NOP56 cDNA ORF clone, Homo sapiens(human)

Gene
Clones
gRNAs

Summary

Gene Symbol	NOP56
Entrez Gene ID	10528
Full Name	NOP56 ribonucleoprotein
Synonyms	NOL5A,SCA36
General protein information	Preferred Names NOP56 ribonucleoprotein Names nucleolar protein 56 NOP56 ribonucleoprotein homolog nucleolar protein 5A (56kDa with KKE/D repeat)
Gene Type	protein-coding
Organism	Homo sapiens(human)
Genome	Chromosome: 20 Map Location: 20p13
Summary	Nop56p is a yeast nucleolar protein that is part of a complex with the nucleolar proteins Nop58p and fibrillarin. Nop56p is required for assembly of the 60S ribosomal subunit and is involved in pre-rRNA processing. The protein encoded by this gene is similar in sequence to Nop56p and is also found in the nucleolus. Expansion of a GGCCTG repeat from 3-8 copies to 1500-2500 copies in an intron of this gene results in spinocerebellar ataxia 36. Multiple transcript variants encoding several different isoforms have been found for this gene, but the full-length nature of most of them has not been determined. [provided by RefSeq, Jul 2016].
Disorder MIM:	614154
Disorder Html:	Spinocerebellar ataxia 36, 614153 (3)

mRNA and Protein(s)

mRNA	Protein	Name
NM_006392.4	NP_006383.2	nucleolar protein 56
NM_006392.3	NP_006383.2	nucleolar protein 56

Pathways from BioSystems

Homologies

	LOC718202	XP_001110561.2
Bos taurus (cattle)	NOP56	NP_001028794.1
Gallus gallus (chicken)	NOP56	NP_001026559.1
Anopheles gambiae (African malaria mosquito)	AgaP_AGAP002063	XP_320984.4
Saccharomyces cerevisiae (baker's yeast)	NOP56	NP_013298.1
Arabidopsis thaliana (thale cress)	AT3G12860	NP_187892.2
Arabidopsis thaliana (thale cress)	NOP56	NP_176007.1
Mus musculus (house mouse)	Nop56	NP_077155.2
Magnaporthe oryzae (rice blast fungus)	MGG_07915	XP_003713157.1
Xenopus tropicalis (tropical clawed frog)	nop56	NP_001184132.1
Pan troglodytes (chimpanzee)	NOP56	NP_001231603.1
Canis lupus familiaris (dog)	NOP56	XP_851724.2
Rattus norvegicus (Norway rat)	Nop56	NP_001020903.1
Caenorhabditis elegans (roundworm)	K07C5.4	NP_505660.1
Oryza sativa (rice)	Os03g0352300	NP_001050122.1
Drosophila melanogaster (fruit fly)	Nop56	NP_651040.3
Neurospora crassa	NCU06943	XP_958049.2
Homo sapiens (human)	NOP56	NP_006383.2
Danio rerio (zebrafish)	nop56	NP_957511.1
Kluyveromyces lactis	KLLA0D12254g	XP_453608.1
Eremothecium gossypii	AGOS_ACL144C	NP_983260.1
Schizosaccharomyces pombe (fission yeast)	SPBC646.10c	NP_595368.1

Gene Ontology
Bibliography

Related articles in PubMed

Genetic and clinical analysis of spinocerebellar ataxia type 36 in Mainland China.
Zeng S, Zeng J, He M, Zeng X, Zhou Y, Liu Z, Xia K, Pan Q, Jiang H, Shen L, Yan X, Tang B, Wang J
Clinical genetics90(2)141-8(2016 Aug)

[Recent advances in clinical and genetic research of spinocerebellar ataxia type 36].
Zeng S, Tang B, Wang J
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics32(6)886-9(2015 Dec)

The Repeat Expansion Diseases: The dark side of DNA repair.
Zhao XN, Usdin K
DNA repair3296-105(2015 Aug)

E-cadherin interactome complexity and robustness resolved by quantitative proteomics.
Guo Z, Neilson LJ, Zhong H, Murray PS, Zanivan S, Zaidel-Bar R
Science signaling7(354)rs7(2014 Dec)

GeneRIFs: Gene References Into Functions What's a GeneRIF?

Genetic and clinical analysis of spinocerebellar ataxia type 36 in Mainland China, with its causative mutation as a hexanucleotide GGCCTG repeat expansion in intron 1 of the NOP56 gene, has been described.
Title: Genetic and clinical analysis of spinocerebellar ataxia type 36 in Mainland China.

Studies indicate that the causative mutation for spinocerebellar ataxias SCA36, namely intronic hexanucleotide GGCCTG expansion in NOP56 gene, has been identified.
Title: [Recent advances in clinical and genetic research of spinocerebellar ataxia type 36].

We newly found intronic hexanucleotide GGCCTG gene expansion in NOP56 gene as the causative mutation in nine unrelated Japanese familial hereditary spinocerebellar ataxia patients
Title: Cognitive and affective impairments of a novel SCA/MND crossroad mutation Asidan.

This study demonistrated that NOP56 mutation is response spinocerebellar ataxia 36 in Spainish family.
Title: 'Costa da Morte' ataxia is spinocerebellar ataxia 36: clinical and genetic characterization.

Expansion of the intronic GGCCTG hexanucleotide repeat in NOP56 causes a unique form of spinocerebellar ataxias, SCA36, which shows not only ataxia but also motor neuron dysfunction.
Title: Expansion of intronic GGCCTG hexanucleotide repeat in NOP56 causes SCA36, a type of spinocerebellar ataxia accompanied by motor neuron involvement.

The following NOP56 gene cDNA ORF clone sequences were retrieved from the NCBI Reference Sequence Database (RefSeq). These sequences represent the protein coding region of the NOP56 cDNA ORF which is encoded by the open reading frame (ORF) sequence. ORF sequences can be delivered in our standard vector, pcDNA3.1⁺/C-(K)DYK or the vector of your choice as an expression/transfection-ready ORF clone. Not the clone you want? Click here to find your clone.

***CloneID	Accession No.	Definition	**Vector	*Turnaround time	Price (USD)
OHu26853	NM_006392.4 Latest version!	Homo sapiens NOP56 ribonucleoprotein (NOP56), transcript variant 1, mRNA.	pcDNA3.1-C-(k)DYK or customized vector	in pcDNA3.1-C-(k)DYK	$219.50-$307.30 $439.00
View Old Accession Versions >>
OHu26853	NM_006392.3	Homo sapiens NOP56 ribonucleoprotein (NOP56), transcript variant 1, mRNA.	pcDNA3.1-C-(k)DYK or customized vector	in pcDNA3.1-C-(k)DYK	$219.50-$307.30 $439.00
Hide Old Accession Versions >>

ORF Online Only Promotion

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

*Business Day

** You may select a custom vector to replace pcDNA3.1+/C-(K)DYK after clone is added to cart.

** GenScript guarantees 100% sequence accuracy of all synthetic DNA constructs we deliver, but we do not guarantee protein expression in your experimental system. Protein expression is influenced by many factors that may vary between experiments or laboratories. In addition, please pay attention to the signal peptide, propeptide and transit peptide in target ORF, which may affect the choice of vector (N/C terminal tag vector).

***One clone ID might be correlated to multiple accession numbers, which share the same CDS sequence.

Reference Sequences (Refseq)

NOP56 ( NM_006392.4 ) cDNA ORF clone, Homo sapiens(human) -> NP_006383.2 Homo sapiens NOP56 ribonucleoprotein (NOP56), transcript variant 1, mRNA.

Price & Availability↑

CloneID	OHu26853
Clone ID Related Accession (Same CDS sequence)	NM_006392.4 , NM_006392.3
Accession Version	NM_006392.4 Latest version!	Documents for ORF clone product in default vector
Sequence Information	ORF Nucleotide Sequence (Length: 1785bp) 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	2019-08-21
Organism	Homo sapiens(human)
Product	nucleolar protein 56
Comment	Comment: REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from DA805367.1, BC104793.1 and BC035369.1. This sequence is a reference standard in the RefSeqGene project. On Nov 22, 2018 this sequence version replaced NM_006392.3. Transcript Variant: This variant (1) represents the protein-coding transcript. 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 :: BX647439.1, SRR3476690.609502.1 [ECO:0000332] RNAseq introns :: single sample supports all introns SAMEA1965299, SAMEA1966682 [ECO:0000348] ##Evidence-Data-END## ##RefSeq-Attributes-START## MANE Ensembl match :: ENST00000329276.10/ ENSP00000370589.3 RefSeq Select criteria :: based on single protein-coding transcript ##RefSeq-Attributes-END## COMPLETENESS: full length.

ATGGTGCTGT TGCACGTGCT GTTTGAGCAC GCGGTCGGCT ACGCGCTGCT GGCGCTGAAG 
GAAGTGGAGG AGATCAGTCT GCTGCAGCCG CAGGTGGAGG AGTCTGTGCT CAACCTGGGC 
AAATTCCACA GCATCGTTCG TCTGGTGGCC TTTTGTCCCT TTGCCTCATC CCAGGTTGCC 
TTGGAAAATG CCAACGCCGT GTCTGAAGGG GTTGTTCATG AGGACCTCCG CCTGCTCTTG 
GAGACCCACC TGCCGTCCAA AAAGAAGAAA GTACTCTTGG GAGTTGGGGA TCCCAAGATT 
GGTGCCGCAA TACAGGAGGA GTTAGGGTAC AACTGCCAGA CTGGAGGAGT CATAGCTGAG 
ATCCTGCGAG GAGTTCGTCT GCACTTCCAC AATCTGGTGA AGGGTCTGAC CGATCTGTCA 
GCTTGTAAAG CACAGCTGGG GCTGGGACAC AGCTATTCCC GTGCCAAAGT TAAGTTTAAT 
GTGAACCGGG TGGACAATAT GATCATCCAG TCCATTAGCC TCCTGGACCA GCTGGATAAG 
GACATCAATA CCTTCTCTAT GCGTGTCAGG GAGTGGTACG GGTATCACTT TCCGGAGCTG 
GTGAAGATCA TCAACGACAA TGCCACATAC TGCCGTCTTG CCCAGTTTAT TGGAAACCGA 
AGGGAACTGA ATGAGGACAA GCTGGAGAAG CTGGAGGAGC TGACAATGGA TGGGGCCAAG 
GCTAAGGCTA TTCTGGATGC CTCACGGTCC TCCATGGGCA TGGACATATC TGCCATTGAC 
TTGATAAACA TCGAGAGCTT CTCCAGTCGT GTGGTGTCTT TATCTGAATA CCGCCAGAGC 
CTACACACTT ACCTGCGCTC CAAGATGAGC CAAGTAGCCC CCAGCCTGTC AGCCCTAATT 
GGGGAAGCGG TAGGTGCACG TCTCATCGCA CATGCTGGCA GCCTCACCAA CCTGGCCAAG 
TATCCAGCAT CCACAGTGCA GATCCTTGGG GCTGAAAAGG CCCTGTTCAG AGCCCTGAAG 
ACAAGGGGTA ACACTCCAAA ATATGGACTC ATTTTCCACT CCACCTTCAT TGGCCGAGCA 
GCTGCCAAGA ACAAAGGCCG CATCTCCCGA TACCTGGCAA ACAAATGCAG TATTGCCTCA 
CGAATCGATT GCTTCTCTGA GGTGCCCACG AGTGTATTCG GGGAGAAGCT TCGAGAACAA 
GTTGAAGAGC GACTGTCCTT CTATGAGACT GGAGAGATAC CACGAAAGAA TCTGGATGTC 
ATGAAGGAAG CAATGGTTCA GGCAGAGGAA GCGGCTGCTG AGATTACTAG GAAGCTGGAG 
AAACAGGAGA AGAAACGCTT AAAGAAGGAA AAGAAACGGC TGGCTGCACT TGCCCTCGCG 
TCTTCAGAAA ACAGCAGTAG TACTCCAGAG GAGTGTGAGG AGATGAGTGA AAAACCCAAA 
AAGAAGAAAA AGCAAAAGCC CCAGGAGGTT CCTCAGGAGA ATGGAATGGA AGACCCATCT 
ATCTCTTTCT CCAAACCCAA GAAAAAGAAA TCTTTTTCCA AGGAGGAGTT GATGAGTAGC 
GATCTTGAAG AGACCGCTGG CAGCACCAGT ATTCCCAAGA GGAAGAAGTC TACACCCAAG 
GAGGAAACAG TTAATGACCC TGAGGAGGCA GGCCACAGAA GTGGCTCCAA GAAAAAGAGG 
AAATTCTCCA AAGAGGAGCC GGTCAGCAGT GGGCCTGAAG AGGCGGTTGG CAAGAGCAGC 
TCCAAGAAGA AGAAAAAGTT CCATAAAGCA TCCCAGGAAG ATTAG

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

RefSeq	NP_006383.2
CDS	30..1814
Translation	MVLLHVLFEHAVGYALLALKEVEEISLLQPQVEESVLNLGKFHSIVRLVAFCPFASSQVALENANAVSEGVVHEDLRLLLETHLPSKKKKVLLGVGDPKIGAAIQEELGYNCQTGGVIAEILRGVRLHFHNLVKGLTDLSACKAQLGLGHSYSRAKVKFNVNRVDNMIIQSISLLDQLDKDINTFSMRVREWYGYHFPELVKIINDNATYCRLAQFIGNRRELNEDKLEKLEELTMDGAKAKAILDASRSSMGMDISAIDLINIESFSSRVVSLSEYRQSLHTYLRSKMSQVAPSLSALIGEAVGARLIAHAGSLTNLAKYPASTVQILGAEKALFRALKTRGNTPKYGLIFHSTFIGRAAAKNKGRISRYLANKCSIASRIDCFSEVPTSVFGEKLREQVEERLSFYETGEIPRKNLDVMKEAMVQAEEAAAEITRKLEKQEKKRLKKEKKRLAALALASSENSSSTPEECEEMSEKPKKKKKQKPQEVPQENGMEDPSISFSKPKKKKSFSKEELMSSDLEETAGSTSIPKRKKSTPKEETVNDPEEAGHRSGSKKKRKFSKEEPVSSGPEEAVGKSSSKKKKKFHKASQED

Target ORF information:

RefSeq Version	NM_006392.4
Organism	Homo sapiens(human)
Definition	Homo sapiens NOP56 ribonucleoprotein (NOP56), transcript variant 1, mRNA.

Target ORF information:

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

NM_006392.4

ORF Insert Sequence:

ATGGTGCTGT TGCACGTGCT GTTTGAGCAC GCGGTCGGCT ACGCGCTGCT GGCGCTGAAG 
GAAGTGGAGG AGATCAGTCT GCTGCAGCCG CAGGTGGAGG AGTCTGTGCT CAACCTGGGC 
AAATTCCACA GCATCGTTCG TCTGGTGGCC TTTTGTCCCT TTGCCTCATC CCAGGTTGCC 
TTGGAAAATG CCAACGCCGT GTCTGAAGGG GTTGTTCATG AGGACCTCCG CCTGCTCTTG 
GAGACCCACC TGCCGTCCAA AAAGAAGAAA GTACTCTTGG GAGTTGGGGA TCCCAAGATT 
GGTGCCGCAA TACAGGAGGA GTTAGGGTAC AACTGCCAGA CTGGAGGAGT CATAGCTGAG 
ATCCTGCGAG GAGTTCGTCT GCACTTCCAC AATCTGGTGA AGGGTCTGAC CGATCTGTCA 
GCTTGTAAAG CACAGCTGGG GCTGGGACAC AGCTATTCCC GTGCCAAAGT TAAGTTTAAT 
GTGAACCGGG TGGACAATAT GATCATCCAG TCCATTAGCC TCCTGGACCA GCTGGATAAG 
GACATCAATA CCTTCTCTAT GCGTGTCAGG GAGTGGTACG GGTATCACTT TCCGGAGCTG 
GTGAAGATCA TCAACGACAA TGCCACATAC TGCCGTCTTG CCCAGTTTAT TGGAAACCGA 
AGGGAACTGA ATGAGGACAA GCTGGAGAAG CTGGAGGAGC TGACAATGGA TGGGGCCAAG 
GCTAAGGCTA TTCTGGATGC CTCACGGTCC TCCATGGGCA TGGACATATC TGCCATTGAC 
TTGATAAACA TCGAGAGCTT CTCCAGTCGT GTGGTGTCTT TATCTGAATA CCGCCAGAGC 
CTACACACTT ACCTGCGCTC CAAGATGAGC CAAGTAGCCC CCAGCCTGTC AGCCCTAATT 
GGGGAAGCGG TAGGTGCACG TCTCATCGCA CATGCTGGCA GCCTCACCAA CCTGGCCAAG 
TATCCAGCAT CCACAGTGCA GATCCTTGGG GCTGAAAAGG CCCTGTTCAG AGCCCTGAAG 
ACAAGGGGTA ACACTCCAAA ATATGGACTC ATTTTCCACT CCACCTTCAT TGGCCGAGCA 
GCTGCCAAGA ACAAAGGCCG CATCTCCCGA TACCTGGCAA ACAAATGCAG TATTGCCTCA 
CGAATCGATT GCTTCTCTGA GGTGCCCACG AGTGTATTCG GGGAGAAGCT TCGAGAACAA 
GTTGAAGAGC GACTGTCCTT CTATGAGACT GGAGAGATAC CACGAAAGAA TCTGGATGTC 
ATGAAGGAAG CAATGGTTCA GGCAGAGGAA GCGGCTGCTG AGATTACTAG GAAGCTGGAG 
AAACAGGAGA AGAAACGCTT AAAGAAGGAA AAGAAACGGC TGGCTGCACT TGCCCTCGCG 
TCTTCAGAAA ACAGCAGTAG TACTCCAGAG GAGTGTGAGG AGATGAGTGA AAAACCCAAA 
AAGAAGAAAA AGCAAAAGCC CCAGGAGGTT CCTCAGGAGA ATGGAATGGA AGACCCATCT 
ATCTCTTTCT CCAAACCCAA GAAAAAGAAA TCTTTTTCCA AGGAGGAGTT GATGAGTAGC 
GATCTTGAAG AGACCGCTGG CAGCACCAGT ATTCCCAAGA GGAAGAAGTC TACACCCAAG 
GAGGAAACAG TTAATGACCC TGAGGAGGCA GGCCACAGAA GTGGCTCCAA GAAAAAGAGG 
AAATTCTCCA AAGAGGAGCC GGTCAGCAGT GGGCCTGAAG AGGCGGTTGG CAAGAGCAGC 
TCCAAGAAGA AGAAAAAGTT CCATAAAGCA TCCCAGGAAG ATTAG

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

NOP56 ( NM_006392.3 ) cDNA ORF clone, Homo sapiens(human) -> NP_006383.2 Homo sapiens NOP56 ribonucleoprotein (NOP56), transcript variant 1, mRNA.

Price & Availability↑

CloneID	OHu26853
Clone ID Related Accession (Same CDS sequence)	NM_006392.4 , NM_006392.3
Accession Version	NM_006392.3	Documents for ORF clone product in default vector
Sequence Information	ORF Nucleotide Sequence (Length: 1785bp) 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	2017-10-02
Organism	Homo sapiens(human)
Product	nucleolar protein 56
Comment	Comment: REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from BC104791.1, DA805367.1, BC104793.1 and BC035369.1. This sequence is a reference standard in the RefSeqGene project. On Aug 10, 2011 this sequence version replaced NM_006392.2. Transcript Variant: This variant (1) represents the protein-coding transcript. 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 :: BC035369.1, SRR1660807.235325.1 [ECO:0000332] RNAseq introns :: single sample supports all introns SAMEA1965299, SAMEA1966682 [ECO:0000348] ##Evidence-Data-END## COMPLETENESS: complete on the 3' end.

ATGGTGCTGT TGCACGTGCT GTTTGAGCAC GCGGTCGGCT ACGCGCTGCT GGCGCTGAAG 
GAAGTGGAGG AGATCAGTCT GCTGCAGCCG CAGGTGGAGG AGTCTGTGCT CAACCTGGGC 
AAATTCCACA GCATCGTTCG TCTGGTGGCC TTTTGTCCCT TTGCCTCATC CCAGGTTGCC 
TTGGAAAATG CCAACGCCGT GTCTGAAGGG GTTGTTCATG AGGACCTCCG CCTGCTCTTG 
GAGACCCACC TGCCGTCCAA AAAGAAGAAA GTACTCTTGG GAGTTGGGGA TCCCAAGATT 
GGTGCCGCAA TACAGGAGGA GTTAGGGTAC AACTGCCAGA CTGGAGGAGT CATAGCTGAG 
ATCCTGCGAG GAGTTCGTCT GCACTTCCAC AATCTGGTGA AGGGTCTGAC CGATCTGTCA 
GCTTGTAAAG CACAGCTGGG GCTGGGACAC AGCTATTCCC GTGCCAAAGT TAAGTTTAAT 
GTGAACCGGG TGGACAATAT GATCATCCAG TCCATTAGCC TCCTGGACCA GCTGGATAAG 
GACATCAATA CCTTCTCTAT GCGTGTCAGG GAGTGGTACG GGTATCACTT TCCGGAGCTG 
GTGAAGATCA TCAACGACAA TGCCACATAC TGCCGTCTTG CCCAGTTTAT TGGAAACCGA 
AGGGAACTGA ATGAGGACAA GCTGGAGAAG CTGGAGGAGC TGACAATGGA TGGGGCCAAG 
GCTAAGGCTA TTCTGGATGC CTCACGGTCC TCCATGGGCA TGGACATATC TGCCATTGAC 
TTGATAAACA TCGAGAGCTT CTCCAGTCGT GTGGTGTCTT TATCTGAATA CCGCCAGAGC 
CTACACACTT ACCTGCGCTC CAAGATGAGC CAAGTAGCCC CCAGCCTGTC AGCCCTAATT 
GGGGAAGCGG TAGGTGCACG TCTCATCGCA CATGCTGGCA GCCTCACCAA CCTGGCCAAG 
TATCCAGCAT CCACAGTGCA GATCCTTGGG GCTGAAAAGG CCCTGTTCAG AGCCCTGAAG 
ACAAGGGGTA ACACTCCAAA ATATGGACTC ATTTTCCACT CCACCTTCAT TGGCCGAGCA 
GCTGCCAAGA ACAAAGGCCG CATCTCCCGA TACCTGGCAA ACAAATGCAG TATTGCCTCA 
CGAATCGATT GCTTCTCTGA GGTGCCCACG AGTGTATTCG GGGAGAAGCT TCGAGAACAA 
GTTGAAGAGC GACTGTCCTT CTATGAGACT GGAGAGATAC CACGAAAGAA TCTGGATGTC 
ATGAAGGAAG CAATGGTTCA GGCAGAGGAA GCGGCTGCTG AGATTACTAG GAAGCTGGAG 
AAACAGGAGA AGAAACGCTT AAAGAAGGAA AAGAAACGGC TGGCTGCACT TGCCCTCGCG 
TCTTCAGAAA ACAGCAGTAG TACTCCAGAG GAGTGTGAGG AGATGAGTGA AAAACCCAAA 
AAGAAGAAAA AGCAAAAGCC CCAGGAGGTT CCTCAGGAGA ATGGAATGGA AGACCCATCT 
ATCTCTTTCT CCAAACCCAA GAAAAAGAAA TCTTTTTCCA AGGAGGAGTT GATGAGTAGC 
GATCTTGAAG AGACCGCTGG CAGCACCAGT ATTCCCAAGA GGAAGAAGTC TACACCCAAG 
GAGGAAACAG TTAATGACCC TGAGGAGGCA GGCCACAGAA GTGGCTCCAA GAAAAAGAGG 
AAATTCTCCA AAGAGGAGCC GGTCAGCAGT GGGCCTGAAG AGGCGGTTGG CAAGAGCAGC 
TCCAAGAAGA AGAAAAAGTT CCATAAAGCA TCCCAGGAAG ATTAG

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

RefSeq	NP_006383.2
CDS	130..1914
Translation	MVLLHVLFEHAVGYALLALKEVEEISLLQPQVEESVLNLGKFHSIVRLVAFCPFASSQVALENANAVSEGVVHEDLRLLLETHLPSKKKKVLLGVGDPKIGAAIQEELGYNCQTGGVIAEILRGVRLHFHNLVKGLTDLSACKAQLGLGHSYSRAKVKFNVNRVDNMIIQSISLLDQLDKDINTFSMRVREWYGYHFPELVKIINDNATYCRLAQFIGNRRELNEDKLEKLEELTMDGAKAKAILDASRSSMGMDISAIDLINIESFSSRVVSLSEYRQSLHTYLRSKMSQVAPSLSALIGEAVGARLIAHAGSLTNLAKYPASTVQILGAEKALFRALKTRGNTPKYGLIFHSTFIGRAAAKNKGRISRYLANKCSIASRIDCFSEVPTSVFGEKLREQVEERLSFYETGEIPRKNLDVMKEAMVQAEEAAAEITRKLEKQEKKRLKKEKKRLAALALASSENSSSTPEECEEMSEKPKKKKKQKPQEVPQENGMEDPSISFSKPKKKKSFSKEELMSSDLEETAGSTSIPKRKKSTPKEETVNDPEEAGHRSGSKKKRKFSKEEPVSSGPEEAVGKSSSKKKKKFHKASQED

Target ORF information:

RefSeq Version	NM_006392.3
Organism	Homo sapiens(human)
Definition	Homo sapiens NOP56 ribonucleoprotein (NOP56), transcript variant 1, mRNA.

Target ORF information:

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

NM_006392.3

ORF Insert Sequence:

ATGGTGCTGT TGCACGTGCT GTTTGAGCAC GCGGTCGGCT ACGCGCTGCT GGCGCTGAAG 
GAAGTGGAGG AGATCAGTCT GCTGCAGCCG CAGGTGGAGG AGTCTGTGCT CAACCTGGGC 
AAATTCCACA GCATCGTTCG TCTGGTGGCC TTTTGTCCCT TTGCCTCATC CCAGGTTGCC 
TTGGAAAATG CCAACGCCGT GTCTGAAGGG GTTGTTCATG AGGACCTCCG CCTGCTCTTG 
GAGACCCACC TGCCGTCCAA AAAGAAGAAA GTACTCTTGG GAGTTGGGGA TCCCAAGATT 
GGTGCCGCAA TACAGGAGGA GTTAGGGTAC AACTGCCAGA CTGGAGGAGT CATAGCTGAG 
ATCCTGCGAG GAGTTCGTCT GCACTTCCAC AATCTGGTGA AGGGTCTGAC CGATCTGTCA 
GCTTGTAAAG CACAGCTGGG GCTGGGACAC AGCTATTCCC GTGCCAAAGT TAAGTTTAAT 
GTGAACCGGG TGGACAATAT GATCATCCAG TCCATTAGCC TCCTGGACCA GCTGGATAAG 
GACATCAATA CCTTCTCTAT GCGTGTCAGG GAGTGGTACG GGTATCACTT TCCGGAGCTG 
GTGAAGATCA TCAACGACAA TGCCACATAC TGCCGTCTTG CCCAGTTTAT TGGAAACCGA 
AGGGAACTGA ATGAGGACAA GCTGGAGAAG CTGGAGGAGC TGACAATGGA TGGGGCCAAG 
GCTAAGGCTA TTCTGGATGC CTCACGGTCC TCCATGGGCA TGGACATATC TGCCATTGAC 
TTGATAAACA TCGAGAGCTT CTCCAGTCGT GTGGTGTCTT TATCTGAATA CCGCCAGAGC 
CTACACACTT ACCTGCGCTC CAAGATGAGC CAAGTAGCCC CCAGCCTGTC AGCCCTAATT 
GGGGAAGCGG TAGGTGCACG TCTCATCGCA CATGCTGGCA GCCTCACCAA CCTGGCCAAG 
TATCCAGCAT CCACAGTGCA GATCCTTGGG GCTGAAAAGG CCCTGTTCAG AGCCCTGAAG 
ACAAGGGGTA ACACTCCAAA ATATGGACTC ATTTTCCACT CCACCTTCAT TGGCCGAGCA 
GCTGCCAAGA ACAAAGGCCG CATCTCCCGA TACCTGGCAA ACAAATGCAG TATTGCCTCA 
CGAATCGATT GCTTCTCTGA GGTGCCCACG AGTGTATTCG GGGAGAAGCT TCGAGAACAA 
GTTGAAGAGC GACTGTCCTT CTATGAGACT GGAGAGATAC CACGAAAGAA TCTGGATGTC 
ATGAAGGAAG CAATGGTTCA GGCAGAGGAA GCGGCTGCTG AGATTACTAG GAAGCTGGAG 
AAACAGGAGA AGAAACGCTT AAAGAAGGAA AAGAAACGGC TGGCTGCACT TGCCCTCGCG 
TCTTCAGAAA ACAGCAGTAG TACTCCAGAG GAGTGTGAGG AGATGAGTGA AAAACCCAAA 
AAGAAGAAAA AGCAAAAGCC CCAGGAGGTT CCTCAGGAGA ATGGAATGGA AGACCCATCT 
ATCTCTTTCT CCAAACCCAA GAAAAAGAAA TCTTTTTCCA AGGAGGAGTT GATGAGTAGC 
GATCTTGAAG AGACCGCTGG CAGCACCAGT ATTCCCAAGA GGAAGAAGTC TACACCCAAG 
GAGGAAACAG TTAATGACCC TGAGGAGGCA GGCCACAGAA GTGGCTCCAA GAAAAAGAGG 
AAATTCTCCA AAGAGGAGCC GGTCAGCAGT GGGCCTGAAG AGGCGGTTGG CAAGAGCAGC 
TCCAAGAAGA AGAAAAAGTT CCATAAAGCA TCCCAGGAAG ATTAG

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

PubMed

Genetic and clinical analysis of spinocerebellar ataxia type 36 in Mainland China.
Clinical genetics90(2)141-8(2016 Aug)
Zeng S,Zeng J,He M,Zeng X,Zhou Y,Liu Z,Xia K,Pan Q,Jiang H,Shen L,Yan X,Tang B,Wang J

[Recent advances in clinical and genetic research of spinocerebellar ataxia type 36].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics32(6)886-9(2015 Dec)
Zeng S,Tang B,Wang J

The Repeat Expansion Diseases: The dark side of DNA repair.
DNA repair3296-105(2015 Aug)
Zhao XN,Usdin K

E-cadherin interactome complexity and robustness resolved by quantitative proteomics.
Science signaling7(354)rs7(2014 Dec)
Guo Z,Neilson LJ,Zhong H,Murray PS,Zanivan S,Zaidel-Bar R

見積依頼

Eメール

japanmarket@genscript.com

電話

03-6811-6572

FAX

03-6811-6573
050-3174-7589(受注専用)

オンラインフォーム

オンライン注文

NOP56 cDNA ORF clone, Homo sapiens(human)

Gene

Clones

gRNAs

Related articles in PubMed

Target ORF information:

Target ORF information:

ORF Insert Sequence:

Target ORF information:

Target ORF information:

ORF Insert Sequence:

見積依頼

Eメール

電話

FAX

オンラインフォーム

サポート

会社情報

サポート

会社情報