MYCN gene cDNA ORF clone, Homo sapiens(human)

mRNA	Protein	Name
NM_005378.5	NP_005369.2	N-myc proto-oncogene protein isoform 1
NM_001293233.1	NP_001280162.1	N-myc proto-oncogene protein isoform 3
NM_001293231.2	NP_001280160.1	N-myc proto-oncogene protein isoform 2
NM_001293231.1	NP_001280160.1	N-myc proto-oncogene protein isoform 2
NM_001293233.2	NP_001280162.1	N-myc proto-oncogene protein isoform 3
NM_001293228.2	NP_001280157.1	N-myc proto-oncogene protein isoform 1
NM_001293228.1	NP_001280157.1	N-myc proto-oncogene protein isoform 1
NM_005378.6	NP_005369.2	N-myc proto-oncogene protein isoform 1
XM_017004168.1	XP_016859657.1	N-myc proto-oncogene protein isoform X1

***CloneID	Accession No.	Definition	**Vector	*Turnaround time	Price (USD)
OHu27902	NM_005378.6 Latest version!	Homo sapiens MYCN proto-oncogene, bHLH transcription factor (MYCN), transcript variant 2, mRNA.	pcDNA3.1-C-(k)DYK or customized vector	in pcDNA3.1-C-(k)DYK	$159.50-$223.30 $319.00
OHu27902	NM_001293228.2 Latest version!	Homo sapiens MYCN proto-oncogene, bHLH transcription factor (MYCN), transcript variant 1, mRNA.	pcDNA3.1-C-(k)DYK or customized vector	in pcDNA3.1-C-(k)DYK	$159.50-$223.30 $319.00
OHu27904	NM_001293233.2 Latest version!	Homo sapiens MYCN proto-oncogene, bHLH transcription factor (MYCN), transcript variant 2, mRNA.	pcDNA3.1-C-(k)DYK or customized vector	in pcDNA3.1-C-(k)DYK	$49.50-$69.30 $99.00
OHu27902	XM_017004168.1 Latest version!	Homo sapiens v-myc avian myelocytomatosis viral oncogene neuroblastoma derived homolog (MYCN), transcript variant X1, mRNA.	pcDNA3.1-C-(k)DYK or customized vector	in pcDNA3.1-C-(k)DYK	$159.50-$223.30 $319.00
OHu27903	NM_001293231.2 Latest version!	Homo sapiens MYCN proto-oncogene, bHLH transcription factor (MYCN), transcript variant 3, mRNA.	pcDNA3.1-C-(k)DYK or customized vector	7-9	$139.30 $199.00
View Old Accession Versions >>
OHu27903	NM_001293231.1	Homo sapiens MYCN proto-oncogene, bHLH transcription factor (MYCN), transcript variant 3, mRNA.	pcDNA3.1-C-(k)DYK or customized vector	7-9	$139.30 $199.00
OHu27904	NM_001293233.1	Homo sapiens MYCN proto-oncogene, bHLH transcription factor (MYCN), transcript variant 2, mRNA.	pcDNA3.1-C-(k)DYK or customized vector	in pcDNA3.1-C-(k)DYK	$49.50-$69.30 $99.00
OHu27902	NM_001293228.1	Homo sapiens MYCN proto-oncogene, bHLH transcription factor (MYCN), transcript variant 1, mRNA.	pcDNA3.1-C-(k)DYK or customized vector	in pcDNA3.1-C-(k)DYK	$159.50-$223.30 $319.00
OHu27902	NM_005378.5	Homo sapiens MYCN proto-oncogene, bHLH transcription factor (MYCN), transcript variant 2, mRNA.	pcDNA3.1-C-(k)DYK or customized vector	in pcDNA3.1-C-(k)DYK	$159.50-$223.30 $319.00
Hide Old Accession Versions >>

MYCN ( NM_005378.5 ) cDNA ORF clone, Homo sapiens(human) -> NP_005369.2 Homo sapiens MYCN proto-oncogene, bHLH transcription factor (MYCN), transcript variant 2, mRNA.

Price & Availability↑

CloneID	OHu27902
Clone ID Related Accession (Same CDS sequence)	NM_005378.5 , NM_001293228.2 , NM_001293228.1 , NM_005378.6 , XM_017004168.1
Accession Version	NM_005378.5	Documents for ORF clone product in default vector
Sequence Information	ORF Nucleotide Sequence (Length: 1395bp) Protein sequence SNP
Vector	pcDNA3.1-C-(k)DYK or customized vector	User Manual
Clone information	Clone Map	MSDS
Tag on pcDNA3.1⁺/C-(K)DYK	C terminal DYKDDDDK tags
ORF Insert Method	CloneEZ™ Seamless cloning technology
Insert Structure	linear
Update Date	2017-12-10
Organism	Homo sapiens(human)
Product	N-myc proto-oncogene protein isoform 1
Comment	Comment: REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from AC010145.10, BC002712.2 and AI962624.1. This sequence is a reference standard in the RefSeqGene project. On Jun 7, 2014 this sequence version replaced NM_005378.4. Transcript Variant: This variant (2) lacks segment 1b in the 5' region, compared to variant 1. This variant includes two open reading frames; the isoform 1 represented by this RefSeq is translated from the downstream open reading frame. This transcript and variant 1 encode the same isoform 1. Sequence Note: This RefSeq record was created from transcript and genomic sequence data to make the sequence consistent with the reference genome assembly. The genomic coordinates used for the transcript record were based on transcript alignments. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Gene record to access additional publications. ##Evidence-Data-START## CDS exon combination :: BC002712.2, BT007384.1 [ECO:0000331] RNAseq introns :: single sample supports all introns SAMEA1965299, SAMEA1970526 [ECO:0000348] ##Evidence-Data-END## COMPLETENESS: complete on the 3' end.

ATGCCGAGCT GCTCCACGTC CACCATGCCG GGCATGATCT GCAAGAACCC AGACCTCGAG 
TTTGACTCGC TACAGCCCTG CTTCTACCCG GACGAAGATG ACTTCTACTT CGGCGGCCCC 
GACTCGACCC CCCCGGGGGA GGACATCTGG AAGAAGTTTG AGCTGCTGCC CACGCCCCCG 
CTGTCGCCCA GCCGTGGCTT CGCGGAGCAC AGCTCCGAGC CCCCGAGCTG GGTCACGGAG 
ATGCTGCTTG AGAACGAGCT GTGGGGCAGC CCGGCCGAGG AGGACGCGTT CGGCCTGGGG 
GGACTGGGTG GCCTCACCCC CAACCCGGTC ATCCTCCAGG ACTGCATGTG GAGCGGCTTC 
TCCGCCCGCG AGAAGCTGGA GCGCGCCGTG AGCGAGAAGC TGCAGCACGG CCGCGGGCCG 
CCAACCGCCG GTTCCACCGC CCAGTCCCCG GGAGCCGGCG CCGCCAGCCC TGCGGGTCGC 
GGGCACGGCG GGGCTGCGGG AGCCGGCCGC GCCGGGGCCG CCCTGCCCGC CGAGCTCGCC 
CACCCGGCCG CCGAGTGCGT GGATCCCGCC GTGGTCTTCC CCTTTCCCGT GAACAAGCGC 
GAGCCAGCGC CCGTGCCCGC AGCCCCGGCC AGTGCCCCGG CGGCGGGCCC TGCGGTCGCC 
TCGGGGGCGG GTATTGCCGC CCCAGCCGGG GCCCCGGGGG TCGCCCCTCC GCGCCCAGGC 
GGCCGCCAGA CCAGCGGCGG CGACCACAAG GCCCTCAGTA CCTCCGGAGA GGACACCCTG 
AGCGATTCAG ATGATGAAGA TGATGAAGAG GAAGATGAAG AGGAAGAAAT CGACGTGGTC 
ACTGTGGAGA AGCGGCGTTC CTCCTCCAAC ACCAAGGCTG TCACCACATT CACCATCACT 
GTGCGTCCCA AGAACGCAGC CCTGGGTCCC GGGAGGGCTC AGTCCAGCGA GCTGATCCTC 
AAACGATGCC TTCCCATCCA CCAGCAGCAC AACTATGCCG CCCCCTCTCC CTACGTGGAG 
AGTGAGGATG CACCCCCACA GAAGAAGATA AAGAGCGAGG CGTCCCCACG TCCGCTCAAG 
AGTGTCATCC CCCCAAAGGC TAAGAGCTTG AGCCCCCGAA ACTCTGACTC GGAGGACAGT 
GAGCGTCGCA GAAACCACAA CATCCTGGAG CGCCAGCGCC GCAACGACCT TCGGTCCAGC 
TTTCTCACGC TCAGGGACCA CGTGCCGGAG TTGGTAAAGA ATGAGAAGGC CGCCAAGGTG 
GTCATTTTGA AAAAGGCCAC TGAGTATGTC CACTCCCTCC AGGCCGAGGA GCACCAGCTT 
TTGCTGGAAA AGGAAAAATT GCAGGCAAGA CAGCAGCAGT TGCTAAAGAA AATTGAACAC 
GCTCGGACTT GCTAG

The stop codons will be deleted if pcDNA3.1⁺/C-(K)DYK vector is selected.

RefSeq	NP_005369.2
CDS	424..1818
Translation	MPSCSTSTMPGMICKNPDLEFDSLQPCFYPDEDDFYFGGPDSTPPGEDIWKKFELLPTPPLSPSRGFAEHSSEPPSWVTEMLLENELWGSPAEEDAFGLGGLGGLTPNPVILQDCMWSGFSAREKLERAVSEKLQHGRGPPTAGSTAQSPGAGAASPAGRGHGGAAGAGRAGAALPAELAHPAAECVDPAVVFPFPVNKREPAPVPAAPASAPAAGPAVASGAGIAAPAGAPGVAPPRPGGRQTSGGDHKALSTSGEDTLSDSDDEDDEEEDEEEEIDVVTVEKRRSSSNTKAVTTFTITVRPKNAALGPGRAQSSELILKRCLPIHQQHNYAAPSPYVESEDAPPQKKIKSEASPRPLKSVIPPKAKSLSPRNSDSEDSERRRNHNILERQRRNDLRSSFLTLRDHVPELVKNEKAAKVVILKKATEYVHSLQAEEHQLLLEKEKLQARQQQLLKKIEHARTC

Target ORF information:

RefSeq Version	NM_005378.5
Organism	Homo sapiens(human)
Definition	Homo sapiens MYCN proto-oncogene, bHLH transcription factor (MYCN), transcript variant 2, mRNA.

Target ORF information:

Epitope	DYKDDDDK
Bacterial selection	AMP^R
Mammalian selection	Neo^R
Vector	pcDNA3.1⁺/C-(K)DYK

NM_005378.5

ORF Insert Sequence:

ATGCCGAGCT GCTCCACGTC CACCATGCCG GGCATGATCT GCAAGAACCC AGACCTCGAG 
TTTGACTCGC TACAGCCCTG CTTCTACCCG GACGAAGATG ACTTCTACTT CGGCGGCCCC 
GACTCGACCC CCCCGGGGGA GGACATCTGG AAGAAGTTTG AGCTGCTGCC CACGCCCCCG 
CTGTCGCCCA GCCGTGGCTT CGCGGAGCAC AGCTCCGAGC CCCCGAGCTG GGTCACGGAG 
ATGCTGCTTG AGAACGAGCT GTGGGGCAGC CCGGCCGAGG AGGACGCGTT CGGCCTGGGG 
GGACTGGGTG GCCTCACCCC CAACCCGGTC ATCCTCCAGG ACTGCATGTG GAGCGGCTTC 
TCCGCCCGCG AGAAGCTGGA GCGCGCCGTG AGCGAGAAGC TGCAGCACGG CCGCGGGCCG 
CCAACCGCCG GTTCCACCGC CCAGTCCCCG GGAGCCGGCG CCGCCAGCCC TGCGGGTCGC 
GGGCACGGCG GGGCTGCGGG AGCCGGCCGC GCCGGGGCCG CCCTGCCCGC CGAGCTCGCC 
CACCCGGCCG CCGAGTGCGT GGATCCCGCC GTGGTCTTCC CCTTTCCCGT GAACAAGCGC 
GAGCCAGCGC CCGTGCCCGC AGCCCCGGCC AGTGCCCCGG CGGCGGGCCC TGCGGTCGCC 
TCGGGGGCGG GTATTGCCGC CCCAGCCGGG GCCCCGGGGG TCGCCCCTCC GCGCCCAGGC 
GGCCGCCAGA CCAGCGGCGG CGACCACAAG GCCCTCAGTA CCTCCGGAGA GGACACCCTG 
AGCGATTCAG ATGATGAAGA TGATGAAGAG GAAGATGAAG AGGAAGAAAT CGACGTGGTC 
ACTGTGGAGA AGCGGCGTTC CTCCTCCAAC ACCAAGGCTG TCACCACATT CACCATCACT 
GTGCGTCCCA AGAACGCAGC CCTGGGTCCC GGGAGGGCTC AGTCCAGCGA GCTGATCCTC 
AAACGATGCC TTCCCATCCA CCAGCAGCAC AACTATGCCG CCCCCTCTCC CTACGTGGAG 
AGTGAGGATG CACCCCCACA GAAGAAGATA AAGAGCGAGG CGTCCCCACG TCCGCTCAAG 
AGTGTCATCC CCCCAAAGGC TAAGAGCTTG AGCCCCCGAA ACTCTGACTC GGAGGACAGT 
GAGCGTCGCA GAAACCACAA CATCCTGGAG CGCCAGCGCC GCAACGACCT TCGGTCCAGC 
TTTCTCACGC TCAGGGACCA CGTGCCGGAG TTGGTAAAGA ATGAGAAGGC CGCCAAGGTG 
GTCATTTTGA AAAAGGCCAC TGAGTATGTC CACTCCCTCC AGGCCGAGGA GCACCAGCTT 
TTGCTGGAAA AGGAAAAATT GCAGGCAAGA CAGCAGCAGT TGCTAAAGAA AATTGAACAC 
GCTCGGACTT GCTAG

The stop codons will be deleted if pcDNA3.1⁺/C-(K)DYK vector is selected.

MYCN ( NM_001293228.2 ) cDNA ORF clone, Homo sapiens(human) -> NP_001280157.1 Homo sapiens MYCN proto-oncogene, bHLH transcription factor (MYCN), transcript variant 1, mRNA.

Price & Availability↑

CloneID	OHu27902
Clone ID Related Accession (Same CDS sequence)	NM_005378.5 , NM_001293228.2 , NM_001293228.1 , NM_005378.6 , XM_017004168.1
Accession Version	NM_001293228.2 Latest version!	Documents for ORF clone product in default vector
Sequence Information	ORF Nucleotide Sequence (Length: 1395bp) Protein sequence SNP
Vector	pcDNA3.1-C-(k)DYK or customized vector	User Manual
Clone information	Clone Map	MSDS
Tag on pcDNA3.1⁺/C-(K)DYK	C terminal DYKDDDDK tags
ORF Insert Method	CloneEZ™ Seamless cloning technology
Insert Structure	linear
Update Date	2020-01-03
Organism	Homo sapiens(human)
Product	N-myc proto-oncogene protein isoform 1
Comment	Comment: REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from AC010145.10 and BC002712.2. On May 31, 2019 this sequence version replaced NM_001293228.1. Transcript Variant: This variant (1) represents the full-length transcript. Its exon 1 includes segments 1a and 1b (also known as exon 1a and exon 1b, PMID: 20017904). This variant encodes isoform 1. Sequence Note: This RefSeq record was created from transcript and genomic sequence data to make the sequence consistent with the reference genome assembly. The genomic coordinates used for the transcript record were based on transcript alignments. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Gene record to access additional publications. ##Evidence-Data-START## CDS exon combination :: BT007384.1, CV811888.1 [ECO:0000331] RNAseq introns :: single sample supports all introns SAMEA2145245, SAMEA2148874 [ECO:0000348] ##Evidence-Data-END##

ATGCCGAGCT GCTCCACGTC CACCATGCCG GGCATGATCT GCAAGAACCC AGACCTCGAG 
TTTGACTCGC TACAGCCCTG CTTCTACCCG GACGAAGATG ACTTCTACTT CGGCGGCCCC 
GACTCGACCC CCCCGGGGGA GGACATCTGG AAGAAGTTTG AGCTGCTGCC CACGCCCCCG 
CTGTCGCCCA GCCGTGGCTT CGCGGAGCAC AGCTCCGAGC CCCCGAGCTG GGTCACGGAG 
ATGCTGCTTG AGAACGAGCT GTGGGGCAGC CCGGCCGAGG AGGACGCGTT CGGCCTGGGG 
GGACTGGGTG GCCTCACCCC CAACCCGGTC ATCCTCCAGG ACTGCATGTG GAGCGGCTTC 
TCCGCCCGCG AGAAGCTGGA GCGCGCCGTG AGCGAGAAGC TGCAGCACGG CCGCGGGCCG 
CCAACCGCCG GTTCCACCGC CCAGTCCCCG GGAGCCGGCG CCGCCAGCCC TGCGGGTCGC 
GGGCACGGCG GGGCTGCGGG AGCCGGCCGC GCCGGGGCCG CCCTGCCCGC CGAGCTCGCC 
CACCCGGCCG CCGAGTGCGT GGATCCCGCC GTGGTCTTCC CCTTTCCCGT GAACAAGCGC 
GAGCCAGCGC CCGTGCCCGC AGCCCCGGCC AGTGCCCCGG CGGCGGGCCC TGCGGTCGCC 
TCGGGGGCGG GTATTGCCGC CCCAGCCGGG GCCCCGGGGG TCGCCCCTCC GCGCCCAGGC 
GGCCGCCAGA CCAGCGGCGG CGACCACAAG GCCCTCAGTA CCTCCGGAGA GGACACCCTG 
AGCGATTCAG ATGATGAAGA TGATGAAGAG GAAGATGAAG AGGAAGAAAT CGACGTGGTC 
ACTGTGGAGA AGCGGCGTTC CTCCTCCAAC ACCAAGGCTG TCACCACATT CACCATCACT 
GTGCGTCCCA AGAACGCAGC CCTGGGTCCC GGGAGGGCTC AGTCCAGCGA GCTGATCCTC 
AAACGATGCC TTCCCATCCA CCAGCAGCAC AACTATGCCG CCCCCTCTCC CTACGTGGAG 
AGTGAGGATG CACCCCCACA GAAGAAGATA AAGAGCGAGG CGTCCCCACG TCCGCTCAAG 
AGTGTCATCC CCCCAAAGGC TAAGAGCTTG AGCCCCCGAA ACTCTGACTC GGAGGACAGT 
GAGCGTCGCA GAAACCACAA CATCCTGGAG CGCCAGCGCC GCAACGACCT TCGGTCCAGC 
TTTCTCACGC TCAGGGACCA CGTGCCGGAG TTGGTAAAGA ATGAGAAGGC CGCCAAGGTG 
GTCATTTTGA AAAAGGCCAC TGAGTATGTC CACTCCCTCC AGGCCGAGGA GCACCAGCTT 
TTGCTGGAAA AGGAAAAATT GCAGGCAAGA CAGCAGCAGT TGCTAAAGAA AATTGAACAC 
GCTCGGACTT GCTAG

The stop codons will be deleted if pcDNA3.1⁺/C-(K)DYK vector is selected.

RefSeq	NP_001280157.1
CDS	622..2016
Translation	MPSCSTSTMPGMICKNPDLEFDSLQPCFYPDEDDFYFGGPDSTPPGEDIWKKFELLPTPPLSPSRGFAEHSSEPPSWVTEMLLENELWGSPAEEDAFGLGGLGGLTPNPVILQDCMWSGFSAREKLERAVSEKLQHGRGPPTAGSTAQSPGAGAASPAGRGHGGAAGAGRAGAALPAELAHPAAECVDPAVVFPFPVNKREPAPVPAAPASAPAAGPAVASGAGIAAPAGAPGVAPPRPGGRQTSGGDHKALSTSGEDTLSDSDDEDDEEEDEEEEIDVVTVEKRRSSSNTKAVTTFTITVRPKNAALGPGRAQSSELILKRCLPIHQQHNYAAPSPYVESEDAPPQKKIKSEASPRPLKSVIPPKAKSLSPRNSDSEDSERRRNHNILERQRRNDLRSSFLTLRDHVPELVKNEKAAKVVILKKATEYVHSLQAEEHQLLLEKEKLQARQQQLLKKIEHARTC

Target ORF information:

RefSeq Version	NM_001293228.2
Organism	Homo sapiens(human)
Definition	Homo sapiens MYCN proto-oncogene, bHLH transcription factor (MYCN), transcript variant 1, mRNA.

Target ORF information:

Epitope	DYKDDDDK
Bacterial selection	AMP^R
Mammalian selection	Neo^R
Vector	pcDNA3.1⁺/C-(K)DYK

NM_001293228.2

ORF Insert Sequence:

ATGCCGAGCT GCTCCACGTC CACCATGCCG GGCATGATCT GCAAGAACCC AGACCTCGAG 
TTTGACTCGC TACAGCCCTG CTTCTACCCG GACGAAGATG ACTTCTACTT CGGCGGCCCC 
GACTCGACCC CCCCGGGGGA GGACATCTGG AAGAAGTTTG AGCTGCTGCC CACGCCCCCG 
CTGTCGCCCA GCCGTGGCTT CGCGGAGCAC AGCTCCGAGC CCCCGAGCTG GGTCACGGAG 
ATGCTGCTTG AGAACGAGCT GTGGGGCAGC CCGGCCGAGG AGGACGCGTT CGGCCTGGGG 
GGACTGGGTG GCCTCACCCC CAACCCGGTC ATCCTCCAGG ACTGCATGTG GAGCGGCTTC 
TCCGCCCGCG AGAAGCTGGA GCGCGCCGTG AGCGAGAAGC TGCAGCACGG CCGCGGGCCG 
CCAACCGCCG GTTCCACCGC CCAGTCCCCG GGAGCCGGCG CCGCCAGCCC TGCGGGTCGC 
GGGCACGGCG GGGCTGCGGG AGCCGGCCGC GCCGGGGCCG CCCTGCCCGC CGAGCTCGCC 
CACCCGGCCG CCGAGTGCGT GGATCCCGCC GTGGTCTTCC CCTTTCCCGT GAACAAGCGC 
GAGCCAGCGC CCGTGCCCGC AGCCCCGGCC AGTGCCCCGG CGGCGGGCCC TGCGGTCGCC 
TCGGGGGCGG GTATTGCCGC CCCAGCCGGG GCCCCGGGGG TCGCCCCTCC GCGCCCAGGC 
GGCCGCCAGA CCAGCGGCGG CGACCACAAG GCCCTCAGTA CCTCCGGAGA GGACACCCTG 
AGCGATTCAG ATGATGAAGA TGATGAAGAG GAAGATGAAG AGGAAGAAAT CGACGTGGTC 
ACTGTGGAGA AGCGGCGTTC CTCCTCCAAC ACCAAGGCTG TCACCACATT CACCATCACT 
GTGCGTCCCA AGAACGCAGC CCTGGGTCCC GGGAGGGCTC AGTCCAGCGA GCTGATCCTC 
AAACGATGCC TTCCCATCCA CCAGCAGCAC AACTATGCCG CCCCCTCTCC CTACGTGGAG 
AGTGAGGATG CACCCCCACA GAAGAAGATA AAGAGCGAGG CGTCCCCACG TCCGCTCAAG 
AGTGTCATCC CCCCAAAGGC TAAGAGCTTG AGCCCCCGAA ACTCTGACTC GGAGGACAGT 
GAGCGTCGCA GAAACCACAA CATCCTGGAG CGCCAGCGCC GCAACGACCT TCGGTCCAGC 
TTTCTCACGC TCAGGGACCA CGTGCCGGAG TTGGTAAAGA ATGAGAAGGC CGCCAAGGTG 
GTCATTTTGA AAAAGGCCAC TGAGTATGTC CACTCCCTCC AGGCCGAGGA GCACCAGCTT 
TTGCTGGAAA AGGAAAAATT GCAGGCAAGA CAGCAGCAGT TGCTAAAGAA AATTGAACAC 
GCTCGGACTT GCTAG

The stop codons will be deleted if pcDNA3.1⁺/C-(K)DYK vector is selected.

MYCN ( NM_001293228.1 ) cDNA ORF clone, Homo sapiens(human) -> NP_001280157.1 Homo sapiens MYCN proto-oncogene, bHLH transcription factor (MYCN), transcript variant 1, mRNA.

Price & Availability↑

CloneID	OHu27902
Clone ID Related Accession (Same CDS sequence)	NM_005378.5 , NM_001293228.2 , NM_001293228.1 , NM_005378.6 , XM_017004168.1
Accession Version	NM_001293228.1	Documents for ORF clone product in default vector
Sequence Information	ORF Nucleotide Sequence (Length: 1395bp) Protein sequence SNP
Vector	pcDNA3.1-C-(k)DYK or customized vector	User Manual
Clone information	Clone Map	MSDS
Tag on pcDNA3.1⁺/C-(K)DYK	C terminal DYKDDDDK tags
ORF Insert Method	CloneEZ™ Seamless cloning technology
Insert Structure	linear
Update Date	2019-02-23
Organism	Homo sapiens(human)
Product	N-myc proto-oncogene protein isoform 1
Comment	Comment: REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from AC010145.10, BC002712.2 and AI962624.1. On Jun 7, 2014 this sequence version replaced XM_006711886.1. Transcript Variant: This variant (1) represents the full-length transcript. Its exon 1 includes segments 1a and 1b (also known as exon 1a and exon 1b, PMID: 20017904). This variant encodes isoform 1. Sequence Note: This RefSeq record was created from transcript and genomic sequence data to make the sequence consistent with the reference genome assembly. The genomic coordinates used for the transcript record were based on transcript alignments. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Gene record to access additional publications. ##Evidence-Data-START## CDS exon combination :: BC002712.2, BT007384.1 [ECO:0000331] RNAseq introns :: single sample supports all introns SAMEA2145245, SAMEA2148874 [ECO:0000348] ##Evidence-Data-END##

ATGCCGAGCT GCTCCACGTC CACCATGCCG GGCATGATCT GCAAGAACCC AGACCTCGAG 
TTTGACTCGC TACAGCCCTG CTTCTACCCG GACGAAGATG ACTTCTACTT CGGCGGCCCC 
GACTCGACCC CCCCGGGGGA GGACATCTGG AAGAAGTTTG AGCTGCTGCC CACGCCCCCG 
CTGTCGCCCA GCCGTGGCTT CGCGGAGCAC AGCTCCGAGC CCCCGAGCTG GGTCACGGAG 
ATGCTGCTTG AGAACGAGCT GTGGGGCAGC CCGGCCGAGG AGGACGCGTT CGGCCTGGGG 
GGACTGGGTG GCCTCACCCC CAACCCGGTC ATCCTCCAGG ACTGCATGTG GAGCGGCTTC 
TCCGCCCGCG AGAAGCTGGA GCGCGCCGTG AGCGAGAAGC TGCAGCACGG CCGCGGGCCG 
CCAACCGCCG GTTCCACCGC CCAGTCCCCG GGAGCCGGCG CCGCCAGCCC TGCGGGTCGC 
GGGCACGGCG GGGCTGCGGG AGCCGGCCGC GCCGGGGCCG CCCTGCCCGC CGAGCTCGCC 
CACCCGGCCG CCGAGTGCGT GGATCCCGCC GTGGTCTTCC CCTTTCCCGT GAACAAGCGC 
GAGCCAGCGC CCGTGCCCGC AGCCCCGGCC AGTGCCCCGG CGGCGGGCCC TGCGGTCGCC 
TCGGGGGCGG GTATTGCCGC CCCAGCCGGG GCCCCGGGGG TCGCCCCTCC GCGCCCAGGC 
GGCCGCCAGA CCAGCGGCGG CGACCACAAG GCCCTCAGTA CCTCCGGAGA GGACACCCTG 
AGCGATTCAG ATGATGAAGA TGATGAAGAG GAAGATGAAG AGGAAGAAAT CGACGTGGTC 
ACTGTGGAGA AGCGGCGTTC CTCCTCCAAC ACCAAGGCTG TCACCACATT CACCATCACT 
GTGCGTCCCA AGAACGCAGC CCTGGGTCCC GGGAGGGCTC AGTCCAGCGA GCTGATCCTC 
AAACGATGCC TTCCCATCCA CCAGCAGCAC AACTATGCCG CCCCCTCTCC CTACGTGGAG 
AGTGAGGATG CACCCCCACA GAAGAAGATA AAGAGCGAGG CGTCCCCACG TCCGCTCAAG 
AGTGTCATCC CCCCAAAGGC TAAGAGCTTG AGCCCCCGAA ACTCTGACTC GGAGGACAGT 
GAGCGTCGCA GAAACCACAA CATCCTGGAG CGCCAGCGCC GCAACGACCT TCGGTCCAGC 
TTTCTCACGC TCAGGGACCA CGTGCCGGAG TTGGTAAAGA ATGAGAAGGC CGCCAAGGTG 
GTCATTTTGA AAAAGGCCAC TGAGTATGTC CACTCCCTCC AGGCCGAGGA GCACCAGCTT 
TTGCTGGAAA AGGAAAAATT GCAGGCAAGA CAGCAGCAGT TGCTAAAGAA AATTGAACAC 
GCTCGGACTT GCTAG

The stop codons will be deleted if pcDNA3.1⁺/C-(K)DYK vector is selected.

RefSeq	NP_001280157.1
CDS	734..2128
Translation	MPSCSTSTMPGMICKNPDLEFDSLQPCFYPDEDDFYFGGPDSTPPGEDIWKKFELLPTPPLSPSRGFAEHSSEPPSWVTEMLLENELWGSPAEEDAFGLGGLGGLTPNPVILQDCMWSGFSAREKLERAVSEKLQHGRGPPTAGSTAQSPGAGAASPAGRGHGGAAGAGRAGAALPAELAHPAAECVDPAVVFPFPVNKREPAPVPAAPASAPAAGPAVASGAGIAAPAGAPGVAPPRPGGRQTSGGDHKALSTSGEDTLSDSDDEDDEEEDEEEEIDVVTVEKRRSSSNTKAVTTFTITVRPKNAALGPGRAQSSELILKRCLPIHQQHNYAAPSPYVESEDAPPQKKIKSEASPRPLKSVIPPKAKSLSPRNSDSEDSERRRNHNILERQRRNDLRSSFLTLRDHVPELVKNEKAAKVVILKKATEYVHSLQAEEHQLLLEKEKLQARQQQLLKKIEHARTC

Target ORF information:

RefSeq Version	NM_001293228.1
Organism	Homo sapiens(human)
Definition	Homo sapiens MYCN proto-oncogene, bHLH transcription factor (MYCN), transcript variant 1, mRNA.

Target ORF information:

Epitope	DYKDDDDK
Bacterial selection	AMP^R
Mammalian selection	Neo^R
Vector	pcDNA3.1⁺/C-(K)DYK

NM_001293228.1

ORF Insert Sequence:

ATGCCGAGCT GCTCCACGTC CACCATGCCG GGCATGATCT GCAAGAACCC AGACCTCGAG 
TTTGACTCGC TACAGCCCTG CTTCTACCCG GACGAAGATG ACTTCTACTT CGGCGGCCCC 
GACTCGACCC CCCCGGGGGA GGACATCTGG AAGAAGTTTG AGCTGCTGCC CACGCCCCCG 
CTGTCGCCCA GCCGTGGCTT CGCGGAGCAC AGCTCCGAGC CCCCGAGCTG GGTCACGGAG 
ATGCTGCTTG AGAACGAGCT GTGGGGCAGC CCGGCCGAGG AGGACGCGTT CGGCCTGGGG 
GGACTGGGTG GCCTCACCCC CAACCCGGTC ATCCTCCAGG ACTGCATGTG GAGCGGCTTC 
TCCGCCCGCG AGAAGCTGGA GCGCGCCGTG AGCGAGAAGC TGCAGCACGG CCGCGGGCCG 
CCAACCGCCG GTTCCACCGC CCAGTCCCCG GGAGCCGGCG CCGCCAGCCC TGCGGGTCGC 
GGGCACGGCG GGGCTGCGGG AGCCGGCCGC GCCGGGGCCG CCCTGCCCGC CGAGCTCGCC 
CACCCGGCCG CCGAGTGCGT GGATCCCGCC GTGGTCTTCC CCTTTCCCGT GAACAAGCGC 
GAGCCAGCGC CCGTGCCCGC AGCCCCGGCC AGTGCCCCGG CGGCGGGCCC TGCGGTCGCC 
TCGGGGGCGG GTATTGCCGC CCCAGCCGGG GCCCCGGGGG TCGCCCCTCC GCGCCCAGGC 
GGCCGCCAGA CCAGCGGCGG CGACCACAAG GCCCTCAGTA CCTCCGGAGA GGACACCCTG 
AGCGATTCAG ATGATGAAGA TGATGAAGAG GAAGATGAAG AGGAAGAAAT CGACGTGGTC 
ACTGTGGAGA AGCGGCGTTC CTCCTCCAAC ACCAAGGCTG TCACCACATT CACCATCACT 
GTGCGTCCCA AGAACGCAGC CCTGGGTCCC GGGAGGGCTC AGTCCAGCGA GCTGATCCTC 
AAACGATGCC TTCCCATCCA CCAGCAGCAC AACTATGCCG CCCCCTCTCC CTACGTGGAG 
AGTGAGGATG CACCCCCACA GAAGAAGATA AAGAGCGAGG CGTCCCCACG TCCGCTCAAG 
AGTGTCATCC CCCCAAAGGC TAAGAGCTTG AGCCCCCGAA ACTCTGACTC GGAGGACAGT 
GAGCGTCGCA GAAACCACAA CATCCTGGAG CGCCAGCGCC GCAACGACCT TCGGTCCAGC 
TTTCTCACGC TCAGGGACCA CGTGCCGGAG TTGGTAAAGA ATGAGAAGGC CGCCAAGGTG 
GTCATTTTGA AAAAGGCCAC TGAGTATGTC CACTCCCTCC AGGCCGAGGA GCACCAGCTT 
TTGCTGGAAA AGGAAAAATT GCAGGCAAGA CAGCAGCAGT TGCTAAAGAA AATTGAACAC 
GCTCGGACTT GCTAG

The stop codons will be deleted if pcDNA3.1⁺/C-(K)DYK vector is selected.

MYCN ( NM_005378.6 ) cDNA ORF clone, Homo sapiens(human) -> NP_005369.2 Homo sapiens MYCN proto-oncogene, bHLH transcription factor (MYCN), transcript variant 2, mRNA.

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CloneID	OHu27902
Clone ID Related Accession (Same CDS sequence)	NM_005378.5 , NM_001293228.2 , NM_001293228.1 , NM_005378.6 , XM_017004168.1
Accession Version	NM_005378.6 Latest version!	Documents for ORF clone product in default vector
Sequence Information	ORF Nucleotide Sequence (Length: 1395bp) Protein sequence SNP
Vector	pcDNA3.1-C-(k)DYK or customized vector	User Manual
Clone information	Clone Map	MSDS
Tag on pcDNA3.1⁺/C-(K)DYK	C terminal DYKDDDDK tags
ORF Insert Method	CloneEZ™ Seamless cloning technology
Insert Structure	linear
Update Date	2019-12-29
Organism	Homo sapiens(human)
Product	N-myc proto-oncogene protein isoform 1
Comment	Comment: REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from AC010145.10 and BC002712.2. This sequence is a reference standard in the RefSeqGene project. On Nov 23, 2018 this sequence version replaced NM_005378.5. Transcript Variant: This variant (2) lacks segment 1b in the 5' region, compared to variant 1. This variant includes two open reading frames; the isoform 1 represented by this RefSeq is translated from the downstream open reading frame. This transcript and variant 1 encode the same isoform 1. Sequence Note: This RefSeq record was created from transcript and genomic sequence data to make the sequence consistent with the reference genome assembly. The genomic coordinates used for the transcript record were based on transcript alignments. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Gene record to access additional publications. ##Evidence-Data-START## CDS exon combination :: BC002712.2, BT007384.1 [ECO:0000331] RNAseq introns :: single sample supports all introns SAMEA1965299, SAMEA1970526 [ECO:0000348] ##Evidence-Data-END## ##RefSeq-Attributes-START## MANE Ensembl match :: ENST00000281043.4/ ENSP00000281043.3 RefSeq Select criteria :: based on manual assertion, conservation, expression, longest protein ##RefSeq-Attributes-END## COMPLETENESS: full length.

ATGCCGAGCT GCTCCACGTC CACCATGCCG GGCATGATCT GCAAGAACCC AGACCTCGAG 
TTTGACTCGC TACAGCCCTG CTTCTACCCG GACGAAGATG ACTTCTACTT CGGCGGCCCC 
GACTCGACCC CCCCGGGGGA GGACATCTGG AAGAAGTTTG AGCTGCTGCC CACGCCCCCG 
CTGTCGCCCA GCCGTGGCTT CGCGGAGCAC AGCTCCGAGC CCCCGAGCTG GGTCACGGAG 
ATGCTGCTTG AGAACGAGCT GTGGGGCAGC CCGGCCGAGG AGGACGCGTT CGGCCTGGGG 
GGACTGGGTG GCCTCACCCC CAACCCGGTC ATCCTCCAGG ACTGCATGTG GAGCGGCTTC 
TCCGCCCGCG AGAAGCTGGA GCGCGCCGTG AGCGAGAAGC TGCAGCACGG CCGCGGGCCG 
CCAACCGCCG GTTCCACCGC CCAGTCCCCG GGAGCCGGCG CCGCCAGCCC TGCGGGTCGC 
GGGCACGGCG GGGCTGCGGG AGCCGGCCGC GCCGGGGCCG CCCTGCCCGC CGAGCTCGCC 
CACCCGGCCG CCGAGTGCGT GGATCCCGCC GTGGTCTTCC CCTTTCCCGT GAACAAGCGC 
GAGCCAGCGC CCGTGCCCGC AGCCCCGGCC AGTGCCCCGG CGGCGGGCCC TGCGGTCGCC 
TCGGGGGCGG GTATTGCCGC CCCAGCCGGG GCCCCGGGGG TCGCCCCTCC GCGCCCAGGC 
GGCCGCCAGA CCAGCGGCGG CGACCACAAG GCCCTCAGTA CCTCCGGAGA GGACACCCTG 
AGCGATTCAG ATGATGAAGA TGATGAAGAG GAAGATGAAG AGGAAGAAAT CGACGTGGTC 
ACTGTGGAGA AGCGGCGTTC CTCCTCCAAC ACCAAGGCTG TCACCACATT CACCATCACT 
GTGCGTCCCA AGAACGCAGC CCTGGGTCCC GGGAGGGCTC AGTCCAGCGA GCTGATCCTC 
AAACGATGCC TTCCCATCCA CCAGCAGCAC AACTATGCCG CCCCCTCTCC CTACGTGGAG 
AGTGAGGATG CACCCCCACA GAAGAAGATA AAGAGCGAGG CGTCCCCACG TCCGCTCAAG 
AGTGTCATCC CCCCAAAGGC TAAGAGCTTG AGCCCCCGAA ACTCTGACTC GGAGGACAGT 
GAGCGTCGCA GAAACCACAA CATCCTGGAG CGCCAGCGCC GCAACGACCT TCGGTCCAGC 
TTTCTCACGC TCAGGGACCA CGTGCCGGAG TTGGTAAAGA ATGAGAAGGC CGCCAAGGTG 
GTCATTTTGA AAAAGGCCAC TGAGTATGTC CACTCCCTCC AGGCCGAGGA GCACCAGCTT 
TTGCTGGAAA AGGAAAAATT GCAGGCAAGA CAGCAGCAGT TGCTAAAGAA AATTGAACAC 
GCTCGGACTT GCTAG

The stop codons will be deleted if pcDNA3.1⁺/C-(K)DYK vector is selected.

RefSeq	NP_005369.2
CDS	312..1706
Translation	MPSCSTSTMPGMICKNPDLEFDSLQPCFYPDEDDFYFGGPDSTPPGEDIWKKFELLPTPPLSPSRGFAEHSSEPPSWVTEMLLENELWGSPAEEDAFGLGGLGGLTPNPVILQDCMWSGFSAREKLERAVSEKLQHGRGPPTAGSTAQSPGAGAASPAGRGHGGAAGAGRAGAALPAELAHPAAECVDPAVVFPFPVNKREPAPVPAAPASAPAAGPAVASGAGIAAPAGAPGVAPPRPGGRQTSGGDHKALSTSGEDTLSDSDDEDDEEEDEEEEIDVVTVEKRRSSSNTKAVTTFTITVRPKNAALGPGRAQSSELILKRCLPIHQQHNYAAPSPYVESEDAPPQKKIKSEASPRPLKSVIPPKAKSLSPRNSDSEDSERRRNHNILERQRRNDLRSSFLTLRDHVPELVKNEKAAKVVILKKATEYVHSLQAEEHQLLLEKEKLQARQQQLLKKIEHARTC

Target ORF information:

RefSeq Version	NM_005378.6
Organism	Homo sapiens(human)
Definition	Homo sapiens MYCN proto-oncogene, bHLH transcription factor (MYCN), transcript variant 2, mRNA.

Target ORF information:

Epitope	DYKDDDDK
Bacterial selection	AMP^R
Mammalian selection	Neo^R
Vector	pcDNA3.1⁺/C-(K)DYK

NM_005378.6

ORF Insert Sequence:

ATGCCGAGCT GCTCCACGTC CACCATGCCG GGCATGATCT GCAAGAACCC AGACCTCGAG 
TTTGACTCGC TACAGCCCTG CTTCTACCCG GACGAAGATG ACTTCTACTT CGGCGGCCCC 
GACTCGACCC CCCCGGGGGA GGACATCTGG AAGAAGTTTG AGCTGCTGCC CACGCCCCCG 
CTGTCGCCCA GCCGTGGCTT CGCGGAGCAC AGCTCCGAGC CCCCGAGCTG GGTCACGGAG 
ATGCTGCTTG AGAACGAGCT GTGGGGCAGC CCGGCCGAGG AGGACGCGTT CGGCCTGGGG 
GGACTGGGTG GCCTCACCCC CAACCCGGTC ATCCTCCAGG ACTGCATGTG GAGCGGCTTC 
TCCGCCCGCG AGAAGCTGGA GCGCGCCGTG AGCGAGAAGC TGCAGCACGG CCGCGGGCCG 
CCAACCGCCG GTTCCACCGC CCAGTCCCCG GGAGCCGGCG CCGCCAGCCC TGCGGGTCGC 
GGGCACGGCG GGGCTGCGGG AGCCGGCCGC GCCGGGGCCG CCCTGCCCGC CGAGCTCGCC 
CACCCGGCCG CCGAGTGCGT GGATCCCGCC GTGGTCTTCC CCTTTCCCGT GAACAAGCGC 
GAGCCAGCGC CCGTGCCCGC AGCCCCGGCC AGTGCCCCGG CGGCGGGCCC TGCGGTCGCC 
TCGGGGGCGG GTATTGCCGC CCCAGCCGGG GCCCCGGGGG TCGCCCCTCC GCGCCCAGGC 
GGCCGCCAGA CCAGCGGCGG CGACCACAAG GCCCTCAGTA CCTCCGGAGA GGACACCCTG 
AGCGATTCAG ATGATGAAGA TGATGAAGAG GAAGATGAAG AGGAAGAAAT CGACGTGGTC 
ACTGTGGAGA AGCGGCGTTC CTCCTCCAAC ACCAAGGCTG TCACCACATT CACCATCACT 
GTGCGTCCCA AGAACGCAGC CCTGGGTCCC GGGAGGGCTC AGTCCAGCGA GCTGATCCTC 
AAACGATGCC TTCCCATCCA CCAGCAGCAC AACTATGCCG CCCCCTCTCC CTACGTGGAG 
AGTGAGGATG CACCCCCACA GAAGAAGATA AAGAGCGAGG CGTCCCCACG TCCGCTCAAG 
AGTGTCATCC CCCCAAAGGC TAAGAGCTTG AGCCCCCGAA ACTCTGACTC GGAGGACAGT 
GAGCGTCGCA GAAACCACAA CATCCTGGAG CGCCAGCGCC GCAACGACCT TCGGTCCAGC 
TTTCTCACGC TCAGGGACCA CGTGCCGGAG TTGGTAAAGA ATGAGAAGGC CGCCAAGGTG 
GTCATTTTGA AAAAGGCCAC TGAGTATGTC CACTCCCTCC AGGCCGAGGA GCACCAGCTT 
TTGCTGGAAA AGGAAAAATT GCAGGCAAGA CAGCAGCAGT TGCTAAAGAA AATTGAACAC 
GCTCGGACTT GCTAG

The stop codons will be deleted if pcDNA3.1⁺/C-(K)DYK vector is selected.

MYCN ( NM_001293233.1 ) cDNA ORF clone, Homo sapiens(human) -> NP_001280162.1 Homo sapiens MYCN proto-oncogene, bHLH transcription factor (MYCN), transcript variant 2, mRNA.

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CloneID	OHu27904
Clone ID Related Accession (Same CDS sequence)	NM_001293233.1 , NM_001293233.2
Accession Version	NM_001293233.1	Documents for ORF clone product in default vector
Sequence Information	ORF Nucleotide Sequence (Length: 339bp) Protein sequence SNP
Vector	pcDNA3.1-C-(k)DYK or customized vector	User Manual
Clone information	Clone Map	MSDS
Tag on pcDNA3.1⁺/C-(K)DYK	C terminal DYKDDDDK tags
ORF Insert Method	CloneEZ™ Seamless cloning technology
Insert Structure	linear
Update Date	2019-02-23
Organism	Homo sapiens(human)
Product	N-myc proto-oncogene protein isoform 3
Comment	Comment: REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from AC010145.10, BC002712.2 and AI962624.1. Transcript Variant: This variant (2) lacks segment 1b in the 5' region, compared to variant 1. This variant includes two open reading frames; the isoform (3, also known as MYCNOT, see PMID: 20017904) represented by this Refseq is translated from the upstream open reading frame. The isoform 3 has an identical N-terminus to that of the isoform 2, and the function of the isoform 3 is currently unknown. Sequence Note: This RefSeq record was created from transcript and genomic sequence data to make the sequence consistent with the reference genome assembly. The genomic coordinates used for the transcript record were based on transcript alignments. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Gene record to access additional publications. ##Evidence-Data-START## CDS exon combination :: BX393747.2, BX353859.2 [ECO:0000331] RNAseq introns :: single sample supports all introns SAMEA1965299, SAMEA1970526 [ECO:0000348] ##Evidence-Data-END## ##RefSeq-Attributes-START## NMD candidate :: PMID: 20017904 ##RefSeq-Attributes-END##

ATGCGGGGGG CTCCTGGGAA CTGTGTTGGA GCCGAGCAAG CGCTAGCCAG GCGCAAGCGC 
GCACAGACTG TAGCCATCCG AGGACACCCC CGCCCCCCCG GCCCACCCGG AGACACCCGC 
GCAGAATCGC CTCCGGATCC CCTGCAGTCG GCGGGAGTGT TGGAGGTCGG CGCCGGCCCC 
CGCCTTCCGC GCCCCCCACG GGAAGGAAGC ACCCCCGGTA TTAAAACGAA CGGGGCGGAA 
AGAAGCCCTC AGTCGCCGGC CGGGAGGCGA GCCGATGCCG AGCTGCTCCA CGTCCACCAT 
GCCGGGCATG ATCTGCAAGA ACCCAGACCT CGAGTTTGA

The stop codons will be deleted if pcDNA3.1⁺/C-(K)DYK vector is selected.

RefSeq	NP_001280162.1
CDS	150..488
Translation	MRGAPGNCVGAEQALARRKRAQTVAIRGHPRPPGPPGDTRAESPPDPLQSAGVLEVGAGPRLPRPPREGSTPGIKTNGAERSPQSPAGRRADAELLHVHHAGHDLQEPRPRV

Target ORF information:

RefSeq Version	NM_001293233.1
Organism	Homo sapiens(human)
Definition	Homo sapiens MYCN proto-oncogene, bHLH transcription factor (MYCN), transcript variant 2, mRNA.

Target ORF information:

Epitope	DYKDDDDK
Bacterial selection	AMP^R
Mammalian selection	Neo^R
Vector	pcDNA3.1⁺/C-(K)DYK

NM_001293233.1

ORF Insert Sequence:

ATGCGGGGGG CTCCTGGGAA CTGTGTTGGA GCCGAGCAAG CGCTAGCCAG GCGCAAGCGC 
GCACAGACTG TAGCCATCCG AGGACACCCC CGCCCCCCCG GCCCACCCGG AGACACCCGC 
GCAGAATCGC CTCCGGATCC CCTGCAGTCG GCGGGAGTGT TGGAGGTCGG CGCCGGCCCC 
CGCCTTCCGC GCCCCCCACG GGAAGGAAGC ACCCCCGGTA TTAAAACGAA CGGGGCGGAA 
AGAAGCCCTC AGTCGCCGGC CGGGAGGCGA GCCGATGCCG AGCTGCTCCA CGTCCACCAT 
GCCGGGCATG ATCTGCAAGA ACCCAGACCT CGAGTTTGA

The stop codons will be deleted if pcDNA3.1⁺/C-(K)DYK vector is selected.

MYCN ( NM_001293233.2 ) cDNA ORF clone, Homo sapiens(human) -> NP_001280162.1 Homo sapiens MYCN proto-oncogene, bHLH transcription factor (MYCN), transcript variant 2, mRNA.

Price & Availability↑

CloneID	OHu27904
Clone ID Related Accession (Same CDS sequence)	NM_001293233.1 , NM_001293233.2
Accession Version	NM_001293233.2 Latest version!	Documents for ORF clone product in default vector
Sequence Information	ORF Nucleotide Sequence (Length: 339bp) Protein sequence SNP
Vector	pcDNA3.1-C-(k)DYK or customized vector	User Manual
Clone information	Clone Map	MSDS
Tag on pcDNA3.1⁺/C-(K)DYK	C terminal DYKDDDDK tags
ORF Insert Method	CloneEZ™ Seamless cloning technology
Insert Structure	linear
Update Date	2019-11-04
Organism	Homo sapiens(human)
Product	N-myc proto-oncogene protein isoform 3
Comment	Comment: REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from AC010145.10 and BC002712.2. On May 31, 2019 this sequence version replaced NM_001293233.1. Transcript Variant: This variant (2) lacks segment 1b in the 5' region, compared to variant 1. This variant includes two open reading frames; the isoform (3, also known as MYCNOT, see PMID: 20017904) represented by this Refseq is translated from the upstream open reading frame. The isoform 3 has an identical N-terminus to that of the isoform 2, and the function of the isoform 3 is currently unknown. Sequence Note: This RefSeq record was created from transcript and genomic sequence data to make the sequence consistent with the reference genome assembly. The genomic coordinates used for the transcript record were based on transcript alignments. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Gene record to access additional publications. ##Evidence-Data-START## CDS exon combination :: BX353859.2, BX393747.2 [ECO:0000331] RNAseq introns :: single sample supports all introns SAMEA1965299, SAMEA1970526 [ECO:0000348] ##Evidence-Data-END## ##RefSeq-Attributes-START## NMD candidate :: PMID: 20017904 ##RefSeq-Attributes-END##

ATGCGGGGGG CTCCTGGGAA CTGTGTTGGA GCCGAGCAAG CGCTAGCCAG GCGCAAGCGC 
GCACAGACTG TAGCCATCCG AGGACACCCC CGCCCCCCCG GCCCACCCGG AGACACCCGC 
GCAGAATCGC CTCCGGATCC CCTGCAGTCG GCGGGAGTGT TGGAGGTCGG CGCCGGCCCC 
CGCCTTCCGC GCCCCCCACG GGAAGGAAGC ACCCCCGGTA TTAAAACGAA CGGGGCGGAA 
AGAAGCCCTC AGTCGCCGGC CGGGAGGCGA GCCGATGCCG AGCTGCTCCA CGTCCACCAT 
GCCGGGCATG ATCTGCAAGA ACCCAGACCT CGAGTTTGA

The stop codons will be deleted if pcDNA3.1⁺/C-(K)DYK vector is selected.

RefSeq	NP_001280162.1
CDS	38..376
Translation	MRGAPGNCVGAEQALARRKRAQTVAIRGHPRPPGPPGDTRAESPPDPLQSAGVLEVGAGPRLPRPPREGSTPGIKTNGAERSPQSPAGRRADAELLHVHHAGHDLQEPRPRV

Target ORF information:

RefSeq Version	NM_001293233.2
Organism	Homo sapiens(human)
Definition	Homo sapiens MYCN proto-oncogene, bHLH transcription factor (MYCN), transcript variant 2, mRNA.

Target ORF information:

Epitope	DYKDDDDK
Bacterial selection	AMP^R
Mammalian selection	Neo^R
Vector	pcDNA3.1⁺/C-(K)DYK

NM_001293233.2

ORF Insert Sequence:

ATGCGGGGGG CTCCTGGGAA CTGTGTTGGA GCCGAGCAAG CGCTAGCCAG GCGCAAGCGC 
GCACAGACTG TAGCCATCCG AGGACACCCC CGCCCCCCCG GCCCACCCGG AGACACCCGC 
GCAGAATCGC CTCCGGATCC CCTGCAGTCG GCGGGAGTGT TGGAGGTCGG CGCCGGCCCC 
CGCCTTCCGC GCCCCCCACG GGAAGGAAGC ACCCCCGGTA TTAAAACGAA CGGGGCGGAA 
AGAAGCCCTC AGTCGCCGGC CGGGAGGCGA GCCGATGCCG AGCTGCTCCA CGTCCACCAT 
GCCGGGCATG ATCTGCAAGA ACCCAGACCT CGAGTTTGA

The stop codons will be deleted if pcDNA3.1⁺/C-(K)DYK vector is selected.

MYCN ( XM_017004168.1 ) cDNA ORF clone, Homo sapiens(human) -> XP_016859657.1 Homo sapiens v-myc avian myelocytomatosis viral oncogene neuroblastoma derived homolog (MYCN), transcript variant X1, mRNA.

Price & Availability↑

CloneID	OHu27902
Clone ID Related Accession (Same CDS sequence)	NM_005378.5 , NM_001293228.2 , NM_001293228.1 , NM_005378.6 , XM_017004168.1
Accession Version	XM_017004168.1 Latest version!	Documents for ORF clone product in default vector
Sequence Information	ORF Nucleotide Sequence (Length: 1395bp) Protein sequence SNP
Vector	pcDNA3.1-C-(k)DYK or customized vector	User Manual
Clone information	Clone Map	MSDS
Tag on pcDNA3.1⁺/C-(K)DYK	C terminal DYKDDDDK tags
ORF Insert Method	CloneEZ™ Seamless cloning technology
Insert Structure	linear
Update Date	2016-06-05
Organism	Homo sapiens(human)
Product	N-myc proto-oncogene protein isoform X1
Comment	Comment: MODEL REFSEQ: This record is predicted by automated computational analysis. This record is derived from a genomic sequence (NC_000002.12) annotated using gene prediction method: Gnomon, supported by mRNA and EST evidence. Also see: Documentation of NCBI's Annotation Process ##Genome-Annotation-Data-START## Annotation Provider :: NCBI Annotation Status :: Full annotation Annotation Version :: Homo sapiens Annotation Release 108 Annotation Pipeline :: NCBI eukaryotic genome annotation pipeline Annotation Software Version :: 7.0 Annotation Method :: Best-placed RefSeq; Gnomon Features Annotated :: Gene; mRNA; CDS; ncRNA ##Genome-Annotation-Data-END##

ATGCCGAGCT GCTCCACGTC CACCATGCCG GGCATGATCT GCAAGAACCC AGACCTCGAG 
TTTGACTCGC TACAGCCCTG CTTCTACCCG GACGAAGATG ACTTCTACTT CGGCGGCCCC 
GACTCGACCC CCCCGGGGGA GGACATCTGG AAGAAGTTTG AGCTGCTGCC CACGCCCCCG 
CTGTCGCCCA GCCGTGGCTT CGCGGAGCAC AGCTCCGAGC CCCCGAGCTG GGTCACGGAG 
ATGCTGCTTG AGAACGAGCT GTGGGGCAGC CCGGCCGAGG AGGACGCGTT CGGCCTGGGG 
GGACTGGGTG GCCTCACCCC CAACCCGGTC ATCCTCCAGG ACTGCATGTG GAGCGGCTTC 
TCCGCCCGCG AGAAGCTGGA GCGCGCCGTG AGCGAGAAGC TGCAGCACGG CCGCGGGCCG 
CCAACCGCCG GTTCCACCGC CCAGTCCCCG GGAGCCGGCG CCGCCAGCCC TGCGGGTCGC 
GGGCACGGCG GGGCTGCGGG AGCCGGCCGC GCCGGGGCCG CCCTGCCCGC CGAGCTCGCC 
CACCCGGCCG CCGAGTGCGT GGATCCCGCC GTGGTCTTCC CCTTTCCCGT GAACAAGCGC 
GAGCCAGCGC CCGTGCCCGC AGCCCCGGCC AGTGCCCCGG CGGCGGGCCC TGCGGTCGCC 
TCGGGGGCGG GTATTGCCGC CCCAGCCGGG GCCCCGGGGG TCGCCCCTCC GCGCCCAGGC 
GGCCGCCAGA CCAGCGGCGG CGACCACAAG GCCCTCAGTA CCTCCGGAGA GGACACCCTG 
AGCGATTCAG ATGATGAAGA TGATGAAGAG GAAGATGAAG AGGAAGAAAT CGACGTGGTC 
ACTGTGGAGA AGCGGCGTTC CTCCTCCAAC ACCAAGGCTG TCACCACATT CACCATCACT 
GTGCGTCCCA AGAACGCAGC CCTGGGTCCC GGGAGGGCTC AGTCCAGCGA GCTGATCCTC 
AAACGATGCC TTCCCATCCA CCAGCAGCAC AACTATGCCG CCCCCTCTCC CTACGTGGAG 
AGTGAGGATG CACCCCCACA GAAGAAGATA AAGAGCGAGG CGTCCCCACG TCCGCTCAAG 
AGTGTCATCC CCCCAAAGGC TAAGAGCTTG AGCCCCCGAA ACTCTGACTC GGAGGACAGT 
GAGCGTCGCA GAAACCACAA CATCCTGGAG CGCCAGCGCC GCAACGACCT TCGGTCCAGC 
TTTCTCACGC TCAGGGACCA CGTGCCGGAG TTGGTAAAGA ATGAGAAGGC CGCCAAGGTG 
GTCATTTTGA AAAAGGCCAC TGAGTATGTC CACTCCCTCC AGGCCGAGGA GCACCAGCTT 
TTGCTGGAAA AGGAAAAATT GCAGGCAAGA CAGCAGCAGT TGCTAAAGAA AATTGAACAC 
GCTCGGACTT GCTAG

The stop codons will be deleted if pcDNA3.1⁺/C-(K)DYK vector is selected.

RefSeq	XP_016859657.1
CDS	255..1649
Translation	MPSCSTSTMPGMICKNPDLEFDSLQPCFYPDEDDFYFGGPDSTPPGEDIWKKFELLPTPPLSPSRGFAEHSSEPPSWVTEMLLENELWGSPAEEDAFGLGGLGGLTPNPVILQDCMWSGFSAREKLERAVSEKLQHGRGPPTAGSTAQSPGAGAASPAGRGHGGAAGAGRAGAALPAELAHPAAECVDPAVVFPFPVNKREPAPVPAAPASAPAAGPAVASGAGIAAPAGAPGVAPPRPGGRQTSGGDHKALSTSGEDTLSDSDDEDDEEEDEEEEIDVVTVEKRRSSSNTKAVTTFTITVRPKNAALGPGRAQSSELILKRCLPIHQQHNYAAPSPYVESEDAPPQKKIKSEASPRPLKSVIPPKAKSLSPRNSDSEDSERRRNHNILERQRRNDLRSSFLTLRDHVPELVKNEKAAKVVILKKATEYVHSLQAEEHQLLLEKEKLQARQQQLLKKIEHARTC

Target ORF information:

RefSeq Version	XM_017004168.1
Organism	Homo sapiens(human)
Definition	Homo sapiens v-myc avian myelocytomatosis viral oncogene neuroblastoma derived homolog (MYCN), transcript variant X1, mRNA.

Target ORF information:

Epitope	DYKDDDDK
Bacterial selection	AMP^R
Mammalian selection	Neo^R
Vector	pcDNA3.1⁺/C-(K)DYK

XM_017004168.1

ORF Insert Sequence:

ATGCCGAGCT GCTCCACGTC CACCATGCCG GGCATGATCT GCAAGAACCC AGACCTCGAG 
TTTGACTCGC TACAGCCCTG CTTCTACCCG GACGAAGATG ACTTCTACTT CGGCGGCCCC 
GACTCGACCC CCCCGGGGGA GGACATCTGG AAGAAGTTTG AGCTGCTGCC CACGCCCCCG 
CTGTCGCCCA GCCGTGGCTT CGCGGAGCAC AGCTCCGAGC CCCCGAGCTG GGTCACGGAG 
ATGCTGCTTG AGAACGAGCT GTGGGGCAGC CCGGCCGAGG AGGACGCGTT CGGCCTGGGG 
GGACTGGGTG GCCTCACCCC CAACCCGGTC ATCCTCCAGG ACTGCATGTG GAGCGGCTTC 
TCCGCCCGCG AGAAGCTGGA GCGCGCCGTG AGCGAGAAGC TGCAGCACGG CCGCGGGCCG 
CCAACCGCCG GTTCCACCGC CCAGTCCCCG GGAGCCGGCG CCGCCAGCCC TGCGGGTCGC 
GGGCACGGCG GGGCTGCGGG AGCCGGCCGC GCCGGGGCCG CCCTGCCCGC CGAGCTCGCC 
CACCCGGCCG CCGAGTGCGT GGATCCCGCC GTGGTCTTCC CCTTTCCCGT GAACAAGCGC 
GAGCCAGCGC CCGTGCCCGC AGCCCCGGCC AGTGCCCCGG CGGCGGGCCC TGCGGTCGCC 
TCGGGGGCGG GTATTGCCGC CCCAGCCGGG GCCCCGGGGG TCGCCCCTCC GCGCCCAGGC 
GGCCGCCAGA CCAGCGGCGG CGACCACAAG GCCCTCAGTA CCTCCGGAGA GGACACCCTG 
AGCGATTCAG ATGATGAAGA TGATGAAGAG GAAGATGAAG AGGAAGAAAT CGACGTGGTC 
ACTGTGGAGA AGCGGCGTTC CTCCTCCAAC ACCAAGGCTG TCACCACATT CACCATCACT 
GTGCGTCCCA AGAACGCAGC CCTGGGTCCC GGGAGGGCTC AGTCCAGCGA GCTGATCCTC 
AAACGATGCC TTCCCATCCA CCAGCAGCAC AACTATGCCG CCCCCTCTCC CTACGTGGAG 
AGTGAGGATG CACCCCCACA GAAGAAGATA AAGAGCGAGG CGTCCCCACG TCCGCTCAAG 
AGTGTCATCC CCCCAAAGGC TAAGAGCTTG AGCCCCCGAA ACTCTGACTC GGAGGACAGT 
GAGCGTCGCA GAAACCACAA CATCCTGGAG CGCCAGCGCC GCAACGACCT TCGGTCCAGC 
TTTCTCACGC TCAGGGACCA CGTGCCGGAG TTGGTAAAGA ATGAGAAGGC CGCCAAGGTG 
GTCATTTTGA AAAAGGCCAC TGAGTATGTC CACTCCCTCC AGGCCGAGGA GCACCAGCTT 
TTGCTGGAAA AGGAAAAATT GCAGGCAAGA CAGCAGCAGT TGCTAAAGAA AATTGAACAC 
GCTCGGACTT GCTAG

The stop codons will be deleted if pcDNA3.1⁺/C-(K)DYK vector is selected.

MYCN ( NM_001293231.2 ) cDNA ORF clone, Homo sapiens(human) -> NP_001280160.1 Homo sapiens MYCN proto-oncogene, bHLH transcription factor (MYCN), transcript variant 3, mRNA.

Price & Availability↑

CloneID	OHu27903
Clone ID Related Accession (Same CDS sequence)	NM_001293231.2 , NM_001293231.1
Accession Version	NM_001293231.2 Latest version!	Documents for ORF clone product in default vector
Sequence Information	ORF Nucleotide Sequence (Length: 762bp) Protein sequence SNP
Vector	pcDNA3.1-C-(k)DYK or customized vector	User Manual
Clone information	Clone Map	MSDS
Tag on pcDNA3.1⁺/C-(K)DYK	C terminal DYKDDDDK tags
ORF Insert Method	CloneEZ™ Seamless cloning technology
Insert Structure	linear
Update Date	2019-11-04
Organism	Homo sapiens(human)
Product	N-myc proto-oncogene protein isoform 2
Comment	Comment: REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from AC010145.10 and BC002712.2. On May 31, 2019 this sequence version replaced NM_001293231.1. Transcript Variant: This variant (3) lacks segment 1b and exon 2, which results in an upstream AUG start codon, compared to variant 1. The resulting isoform (2) has a shorter and distinct N-terminus, compared to isoform 1. Sequence Note: This RefSeq record was created from transcript and genomic sequence data to make the sequence consistent with the reference genome assembly. The genomic coordinates used for the transcript record were based on transcript alignments. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Gene record to access additional publications. ##Evidence-Data-START## Transcript exon combination :: BE382888.1, BI194921.1 [ECO:0000332] ##Evidence-Data-END##

ATGCGGGGGG CTCCTGGGAA CTGTGTTGGA GCCGAGCAAG CGCTAGCCAG GCGCAAGCGC 
GCACAGACTG TAGCCATCCG AGGACACCCC CGCCCCCCCG GCCCACCCGG AGACACCCGC 
GCAGAATCGC CTCCGGATCC CCTGCAGTCG GCGGGAGATG ATGAAGATGA TGAAGAGGAA 
GATGAAGAGG AAGAAATCGA CGTGGTCACT GTGGAGAAGC GGCGTTCCTC CTCCAACACC 
AAGGCTGTCA CCACATTCAC CATCACTGTG CGTCCCAAGA ACGCAGCCCT GGGTCCCGGG 
AGGGCTCAGT CCAGCGAGCT GATCCTCAAA CGATGCCTTC CCATCCACCA GCAGCACAAC 
TATGCCGCCC CCTCTCCCTA CGTGGAGAGT GAGGATGCAC CCCCACAGAA GAAGATAAAG 
AGCGAGGCGT CCCCACGTCC GCTCAAGAGT GTCATCCCCC CAAAGGCTAA GAGCTTGAGC 
CCCCGAAACT CTGACTCGGA GGACAGTGAG CGTCGCAGAA ACCACAACAT CCTGGAGCGC 
CAGCGCCGCA ACGACCTTCG GTCCAGCTTT CTCACGCTCA GGGACCACGT GCCGGAGTTG 
GTAAAGAATG AGAAGGCCGC CAAGGTGGTC ATTTTGAAAA AGGCCACTGA GTATGTCCAC 
TCCCTCCAGG CCGAGGAGCA CCAGCTTTTG CTGGAAAAGG AAAAATTGCA GGCAAGACAG 
CAGCAGTTGC TAAAGAAAAT TGAACACGCT CGGACTTGCT AG

The stop codons will be deleted if pcDNA3.1⁺/C-(K)DYK vector is selected.

RefSeq	NP_001280160.1
CDS	38..799
Translation	MRGAPGNCVGAEQALARRKRAQTVAIRGHPRPPGPPGDTRAESPPDPLQSAGDDEDDEEEDEEEEIDVVTVEKRRSSSNTKAVTTFTITVRPKNAALGPGRAQSSELILKRCLPIHQQHNYAAPSPYVESEDAPPQKKIKSEASPRPLKSVIPPKAKSLSPRNSDSEDSERRRNHNILERQRRNDLRSSFLTLRDHVPELVKNEKAAKVVILKKATEYVHSLQAEEHQLLLEKEKLQARQQQLLKKIEHARTC

Target ORF information:

RefSeq Version	NM_001293231.2
Organism	Homo sapiens(human)
Definition	Homo sapiens MYCN proto-oncogene, bHLH transcription factor (MYCN), transcript variant 3, mRNA.

Target ORF information:

Epitope	DYKDDDDK
Bacterial selection	AMP^R
Mammalian selection	Neo^R
Vector	pcDNA3.1⁺/C-(K)DYK

NM_001293231.2

ORF Insert Sequence:

ATGCGGGGGG CTCCTGGGAA CTGTGTTGGA GCCGAGCAAG CGCTAGCCAG GCGCAAGCGC 
GCACAGACTG TAGCCATCCG AGGACACCCC CGCCCCCCCG GCCCACCCGG AGACACCCGC 
GCAGAATCGC CTCCGGATCC CCTGCAGTCG GCGGGAGATG ATGAAGATGA TGAAGAGGAA 
GATGAAGAGG AAGAAATCGA CGTGGTCACT GTGGAGAAGC GGCGTTCCTC CTCCAACACC 
AAGGCTGTCA CCACATTCAC CATCACTGTG CGTCCCAAGA ACGCAGCCCT GGGTCCCGGG 
AGGGCTCAGT CCAGCGAGCT GATCCTCAAA CGATGCCTTC CCATCCACCA GCAGCACAAC 
TATGCCGCCC CCTCTCCCTA CGTGGAGAGT GAGGATGCAC CCCCACAGAA GAAGATAAAG 
AGCGAGGCGT CCCCACGTCC GCTCAAGAGT GTCATCCCCC CAAAGGCTAA GAGCTTGAGC 
CCCCGAAACT CTGACTCGGA GGACAGTGAG CGTCGCAGAA ACCACAACAT CCTGGAGCGC 
CAGCGCCGCA ACGACCTTCG GTCCAGCTTT CTCACGCTCA GGGACCACGT GCCGGAGTTG 
GTAAAGAATG AGAAGGCCGC CAAGGTGGTC ATTTTGAAAA AGGCCACTGA GTATGTCCAC 
TCCCTCCAGG CCGAGGAGCA CCAGCTTTTG CTGGAAAAGG AAAAATTGCA GGCAAGACAG 
CAGCAGTTGC TAAAGAAAAT TGAACACGCT CGGACTTGCT AG

The stop codons will be deleted if pcDNA3.1⁺/C-(K)DYK vector is selected.

MYCN ( NM_001293231.1 ) cDNA ORF clone, Homo sapiens(human) -> NP_001280160.1 Homo sapiens MYCN proto-oncogene, bHLH transcription factor (MYCN), transcript variant 3, mRNA.

Price & Availability↑

CloneID	OHu27903
Clone ID Related Accession (Same CDS sequence)	NM_001293231.2 , NM_001293231.1
Accession Version	NM_001293231.1	Documents for ORF clone product in default vector
Sequence Information	ORF Nucleotide Sequence (Length: 762bp) Protein sequence SNP
Vector	pcDNA3.1-C-(k)DYK or customized vector	User Manual
Clone information	Clone Map	MSDS
Tag on pcDNA3.1⁺/C-(K)DYK	C terminal DYKDDDDK tags
ORF Insert Method	CloneEZ™ Seamless cloning technology
Insert Structure	linear
Update Date	2019-02-23
Organism	Homo sapiens(human)
Product	N-myc proto-oncogene protein isoform 2
Comment	Comment: REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from AC010145.10, BC002712.2 and AI962624.1. Transcript Variant: This variant (3) lacks segment 1b and exon 2, which results in an upstream AUG start codon, compared to variant 1. The resulting isoform (2) has a shorter and distinct N-terminus, compared to isoform 1. Sequence Note: This RefSeq record was created from transcript and genomic sequence data to make the sequence consistent with the reference genome assembly. The genomic coordinates used for the transcript record were based on transcript alignments. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Gene record to access additional publications. ##Evidence-Data-START## Transcript exon combination :: BE382888.1, BI194921.1 [ECO:0000332] ##Evidence-Data-END##

ATGCGGGGGG CTCCTGGGAA CTGTGTTGGA GCCGAGCAAG CGCTAGCCAG GCGCAAGCGC 
GCACAGACTG TAGCCATCCG AGGACACCCC CGCCCCCCCG GCCCACCCGG AGACACCCGC 
GCAGAATCGC CTCCGGATCC CCTGCAGTCG GCGGGAGATG ATGAAGATGA TGAAGAGGAA 
GATGAAGAGG AAGAAATCGA CGTGGTCACT GTGGAGAAGC GGCGTTCCTC CTCCAACACC 
AAGGCTGTCA CCACATTCAC CATCACTGTG CGTCCCAAGA ACGCAGCCCT GGGTCCCGGG 
AGGGCTCAGT CCAGCGAGCT GATCCTCAAA CGATGCCTTC CCATCCACCA GCAGCACAAC 
TATGCCGCCC CCTCTCCCTA CGTGGAGAGT GAGGATGCAC CCCCACAGAA GAAGATAAAG 
AGCGAGGCGT CCCCACGTCC GCTCAAGAGT GTCATCCCCC CAAAGGCTAA GAGCTTGAGC 
CCCCGAAACT CTGACTCGGA GGACAGTGAG CGTCGCAGAA ACCACAACAT CCTGGAGCGC 
CAGCGCCGCA ACGACCTTCG GTCCAGCTTT CTCACGCTCA GGGACCACGT GCCGGAGTTG 
GTAAAGAATG AGAAGGCCGC CAAGGTGGTC ATTTTGAAAA AGGCCACTGA GTATGTCCAC 
TCCCTCCAGG CCGAGGAGCA CCAGCTTTTG CTGGAAAAGG AAAAATTGCA GGCAAGACAG 
CAGCAGTTGC TAAAGAAAAT TGAACACGCT CGGACTTGCT AG

The stop codons will be deleted if pcDNA3.1⁺/C-(K)DYK vector is selected.

RefSeq	NP_001280160.1
CDS	150..911
Translation	MRGAPGNCVGAEQALARRKRAQTVAIRGHPRPPGPPGDTRAESPPDPLQSAGDDEDDEEEDEEEEIDVVTVEKRRSSSNTKAVTTFTITVRPKNAALGPGRAQSSELILKRCLPIHQQHNYAAPSPYVESEDAPPQKKIKSEASPRPLKSVIPPKAKSLSPRNSDSEDSERRRNHNILERQRRNDLRSSFLTLRDHVPELVKNEKAAKVVILKKATEYVHSLQAEEHQLLLEKEKLQARQQQLLKKIEHARTC

Target ORF information:

RefSeq Version	NM_001293231.1
Organism	Homo sapiens(human)
Definition	Homo sapiens MYCN proto-oncogene, bHLH transcription factor (MYCN), transcript variant 3, mRNA.

Target ORF information:

Epitope	DYKDDDDK
Bacterial selection	AMP^R
Mammalian selection	Neo^R
Vector	pcDNA3.1⁺/C-(K)DYK

NM_001293231.1

ORF Insert Sequence:

ATGCGGGGGG CTCCTGGGAA CTGTGTTGGA GCCGAGCAAG CGCTAGCCAG GCGCAAGCGC 
GCACAGACTG TAGCCATCCG AGGACACCCC CGCCCCCCCG GCCCACCCGG AGACACCCGC 
GCAGAATCGC CTCCGGATCC CCTGCAGTCG GCGGGAGATG ATGAAGATGA TGAAGAGGAA 
GATGAAGAGG AAGAAATCGA CGTGGTCACT GTGGAGAAGC GGCGTTCCTC CTCCAACACC 
AAGGCTGTCA CCACATTCAC CATCACTGTG CGTCCCAAGA ACGCAGCCCT GGGTCCCGGG 
AGGGCTCAGT CCAGCGAGCT GATCCTCAAA CGATGCCTTC CCATCCACCA GCAGCACAAC 
TATGCCGCCC CCTCTCCCTA CGTGGAGAGT GAGGATGCAC CCCCACAGAA GAAGATAAAG 
AGCGAGGCGT CCCCACGTCC GCTCAAGAGT GTCATCCCCC CAAAGGCTAA GAGCTTGAGC 
CCCCGAAACT CTGACTCGGA GGACAGTGAG CGTCGCAGAA ACCACAACAT CCTGGAGCGC 
CAGCGCCGCA ACGACCTTCG GTCCAGCTTT CTCACGCTCA GGGACCACGT GCCGGAGTTG 
GTAAAGAATG AGAAGGCCGC CAAGGTGGTC ATTTTGAAAA AGGCCACTGA GTATGTCCAC 
TCCCTCCAGG CCGAGGAGCA CCAGCTTTTG CTGGAAAAGG AAAAATTGCA GGCAAGACAG 
CAGCAGTTGC TAAAGAAAAT TGAACACGCT CGGACTTGCT AG

The stop codons will be deleted if pcDNA3.1⁺/C-(K)DYK vector is selected.

Gene Symbol	MYCN
Entrez Gene ID	4613
Full Name	MYCN proto-oncogene, bHLH transcription factor
Synonyms	MODED,N-myc,NMYC,ODED,bHLHe37
General protein information	Preferred Names MYCN proto-oncogene, bHLH transcription factor Names N-myc proto-oncogene protein class E basic helix-loop-helix protein 37 neuroblastoma MYC oncogene neuroblastoma-derived v-myc avian myelocytomatosis viral related oncogene oncogene NMYC v-myc avian myelocytomatosis viral oncogene neuroblastoma derived homolog
Gene Type	protein-coding
Organism	Homo sapiens(human)
Genome	Chromosome: 2 Map Location: 2p24.3
Summary	This gene is a member of the MYC family and encodes a protein with a basic helix-loop-helix (bHLH) domain. This protein is located in the nucleus and must dimerize with another bHLH protein in order to bind DNA. Amplification of this gene is associated with a variety of tumors, most notably neuroblastomas. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2014].
Disorder MIM:	164840
Disorder Html:	Feingold syndrome 1, 164280 (3)

Homo sapiens (human)	MYCN	NP_005369.2
	MYCN	XP_001091369.2
Mus musculus (house mouse)	Mycn	NP_032735.3
Gallus gallus (chicken)	MYCN	NP_001026262.1
Pan troglodytes (chimpanzee)	MYCN	XP_001162405.1
Canis lupus familiaris (dog)	MYCN	XP_005630203.1
Rattus norvegicus (Norway rat)	Mycn	NP_001013114.1
Danio rerio (zebrafish)	mycn	NP_997779.1
Bos taurus (cattle)	MYCN	XP_002691569.1
Xenopus tropicalis (tropical clawed frog)	mycn	NP_001006874.1

Next-day Shipping ORF Clones ( in default vector with tag)
1 Clone	30% OFF
2-4 Clone	40% OFF
5 or more Clone	50% OFF
All Other ORF Clones
30% OFF

MYCN cDNA ORF clone, Homo sapiens(human)

Gene

Clones

gRNAs

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