BSX cDNA ORF clone, Homo sapiens(human)

The following BSX gene cDNA ORF clone sequences were retrieved from the NCBI Reference Sequence Database (RefSeq). These sequences represent the protein coding region of the BSX 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) Select
OHu29968 NM_001098169.2
Latest version!
Homo sapiens brain specific homeobox (BSX), mRNA. pcDNA3.1-C-(k)DYK or customized vector
in pcDNA3.1-C-(k)DYK
$49.50-$69.30
$99.00
View Old Accession Versions >>
OHu29968 NM_001098169.1 Homo sapiens brain specific homeobox (BSX), mRNA. pcDNA3.1-C-(k)DYK or customized vector
in pcDNA3.1-C-(k)DYK
$49.50-$69.30
$99.00
Hide Old Accession Versions >>

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** 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)
    CloneID OHu29968
    Clone ID Related Accession (Same CDS sequence) NM_001098169.2 , NM_001098169.1
    Accession Version NM_001098169.2 Latest version! Documents for ORF clone product in default vector
    Sequence Information ORF Nucleotide Sequence (Length: 702bp)
    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 2019-12-20
    Organism Homo sapiens(human)
    Product brain-specific homeobox protein homolog
    Comment Comment: VALIDATED REFSEQ: This record has undergone validation or preliminary review. The reference sequence was derived from AP003040.2. On May 17, 2019 this sequence version replaced NM_001098169.1. Sequence Note: The RefSeq transcript and protein were derived from genomic sequence to make the sequence consistent with the reference genome assembly. The genomic coordinates used for the transcript record were based on alignments. ##RefSeq-Attributes-START## MANE Ensembl match :: ENST00000343035.3/ ENSP00000344285.2 RefSeq Select criteria :: based on single protein-coding transcript ##RefSeq-Attributes-END##

    1
    61
    121
    181
    241
    301
    361
    421
    481
    541
    601
    661
    ATGAATCTCA ACTTCACCTC TCCTCTACAC CCGGCGTCTT CTCAGAGGCC CACATCCTTC 
    TTCATCGAGG ACATCCTGCT GCACAAGCCC AAGCCGCTGA GAGAGGTGGC CCCAGACCAT
    TTCGCCAGCT CTCTGGCCTC TCGGGTGCCT CTGCTAGACT ATGGCTACCC CCTCATGCCC
    ACACCCACCC TCTTGGCTCC TCACGCCCAT CACCCTCTGC ATAAGGGAGA CCACCATCAT
    CCTTATTTCC TCACCACCTC GGGGATGCCA GTCCCAGCGC TGTTCCCGCA CCCGCAGCAC
    GCGGAGCTGC CGGGGAAGCA CTGCCGCCGC CGCAAAGCCC GCACGGTTTT CTCTGACTCG
    CAGCTCTCGG GCTTGGAGAA GAGGTTCGAG ATCCAGCGCT ACCTGTCCAC GCCAGAACGA
    GTGGAGCTGG CCACGGCCCT CAGCCTGTCC GAGACGCAGG TGAAAACGTG GTTCCAGAAC
    CGGCGGATGA AGCATAAAAA GCAACTGCGG AAAAGCCAAG ACGAACCCAA AGCACCAGAC
    GGGCCAGAAA GCCCCGAGGG CAGCCCCCGC GGTTCAGAGG CCGCCACCGC CGCCGAGGCT
    CGGCTGAGCC TGCCCGCCGG TCCCTTCGTG CTGACCGAGC CAGAGGACGA GGTGGACATT
    GGAGACGAGG GGGAGCTGGG CTCAGGGCCG CACGTGCTCT GA

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

    RefSeq NP_001091639.1
    CDS164..865
    Translation

    Target ORF information:

    RefSeq Version NM_001098169.2
    Organism Homo sapiens(human)
    Definition Homo sapiens brain specific homeobox (BSX), mRNA.

    Target ORF information:

    Epitope DYKDDDDK
    Bacterial selection AMPR
    Mammalian selection NeoR
    Vector pcDNA3.1+/C-(K)DYK
    NM_001098169.2

    ORF Insert Sequence:

    1
    61
    121
    181
    241
    301
    361
    421
    481
    541
    601
    661
    ATGAATCTCA ACTTCACCTC TCCTCTACAC CCGGCGTCTT CTCAGAGGCC CACATCCTTC 
    TTCATCGAGG ACATCCTGCT GCACAAGCCC AAGCCGCTGA GAGAGGTGGC CCCAGACCAT
    TTCGCCAGCT CTCTGGCCTC TCGGGTGCCT CTGCTAGACT ATGGCTACCC CCTCATGCCC
    ACACCCACCC TCTTGGCTCC TCACGCCCAT CACCCTCTGC ATAAGGGAGA CCACCATCAT
    CCTTATTTCC TCACCACCTC GGGGATGCCA GTCCCAGCGC TGTTCCCGCA CCCGCAGCAC
    GCGGAGCTGC CGGGGAAGCA CTGCCGCCGC CGCAAAGCCC GCACGGTTTT CTCTGACTCG
    CAGCTCTCGG GCTTGGAGAA GAGGTTCGAG ATCCAGCGCT ACCTGTCCAC GCCAGAACGA
    GTGGAGCTGG CCACGGCCCT CAGCCTGTCC GAGACGCAGG TGAAAACGTG GTTCCAGAAC
    CGGCGGATGA AGCATAAAAA GCAACTGCGG AAAAGCCAAG ACGAACCCAA AGCACCAGAC
    GGGCCAGAAA GCCCCGAGGG CAGCCCCCGC GGTTCAGAGG CCGCCACCGC CGCCGAGGCT
    CGGCTGAGCC TGCCCGCCGG TCCCTTCGTG CTGACCGAGC CAGAGGACGA GGTGGACATT
    GGAGACGAGG GGGAGCTGGG CTCAGGGCCG CACGTGCTCT GA

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

    CloneID OHu29968
    Clone ID Related Accession (Same CDS sequence) NM_001098169.2 , NM_001098169.1
    Accession Version NM_001098169.1 Documents for ORF clone product in default vector
    Sequence Information ORF Nucleotide Sequence (Length: 702bp)
    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 2018-06-23
    Organism Homo sapiens(human)
    Product brain-specific homeobox protein homolog
    Comment Comment: VALIDATED REFSEQ: This record has undergone validation or preliminary review. The reference sequence was derived from AP003040.2 and AB231738.1. On or before May 23, 2007 this sequence version replaced XM_372433.2, XM_939530.1.

    1
    61
    121
    181
    241
    301
    361
    421
    481
    541
    601
    661
    ATGAATCTCA ACTTCACCTC TCCTCTACAC CCGGCGTCTT CTCAGAGGCC CACATCCTTC 
    TTCATCGAGG ACATCCTGCT GCACAAGCCC AAGCCGCTGA GAGAGGTGGC CCCAGACCAT
    TTCGCCAGCT CTCTGGCCTC TCGGGTGCCT CTGCTAGACT ATGGCTACCC CCTCATGCCC
    ACACCCACCC TCTTGGCTCC TCACGCCCAT CACCCTCTGC ATAAGGGAGA CCACCATCAT
    CCTTATTTCC TCACCACCTC GGGGATGCCA GTCCCAGCGC TGTTCCCGCA CCCGCAGCAC
    GCGGAGCTGC CGGGGAAGCA CTGCCGCCGC CGCAAAGCCC GCACGGTTTT CTCTGACTCG
    CAGCTCTCGG GCTTGGAGAA GAGGTTCGAG ATCCAGCGCT ACCTGTCCAC GCCAGAACGA
    GTGGAGCTGG CCACGGCCCT CAGCCTGTCC GAGACGCAGG TGAAAACGTG GTTCCAGAAC
    CGGCGGATGA AGCATAAAAA GCAACTGCGG AAAAGCCAAG ACGAACCCAA AGCACCAGAC
    GGGCCAGAAA GCCCCGAGGG CAGCCCCCGC GGTTCAGAGG CCGCCACCGC CGCCGAGGCT
    CGGCTGAGCC TGCCCGCCGG TCCCTTCGTG CTGACCGAGC CAGAGGACGA GGTGGACATT
    GGAGACGAGG GGGAGCTGGG CTCAGGGCCG CACGTGCTCT GA

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

    RefSeq NP_001091639.1
    CDS1..702
    Translation

    Target ORF information:

    RefSeq Version NM_001098169.1
    Organism Homo sapiens(human)
    Definition Homo sapiens brain specific homeobox (BSX), mRNA.

    Target ORF information:

    Epitope DYKDDDDK
    Bacterial selection AMPR
    Mammalian selection NeoR
    Vector pcDNA3.1+/C-(K)DYK
    NM_001098169.1

    ORF Insert Sequence:

    1
    61
    121
    181
    241
    301
    361
    421
    481
    541
    601
    661
    ATGAATCTCA ACTTCACCTC TCCTCTACAC CCGGCGTCTT CTCAGAGGCC CACATCCTTC 
    TTCATCGAGG ACATCCTGCT GCACAAGCCC AAGCCGCTGA GAGAGGTGGC CCCAGACCAT
    TTCGCCAGCT CTCTGGCCTC TCGGGTGCCT CTGCTAGACT ATGGCTACCC CCTCATGCCC
    ACACCCACCC TCTTGGCTCC TCACGCCCAT CACCCTCTGC ATAAGGGAGA CCACCATCAT
    CCTTATTTCC TCACCACCTC GGGGATGCCA GTCCCAGCGC TGTTCCCGCA CCCGCAGCAC
    GCGGAGCTGC CGGGGAAGCA CTGCCGCCGC CGCAAAGCCC GCACGGTTTT CTCTGACTCG
    CAGCTCTCGG GCTTGGAGAA GAGGTTCGAG ATCCAGCGCT ACCTGTCCAC GCCAGAACGA
    GTGGAGCTGG CCACGGCCCT CAGCCTGTCC GAGACGCAGG TGAAAACGTG GTTCCAGAAC
    CGGCGGATGA AGCATAAAAA GCAACTGCGG AAAAGCCAAG ACGAACCCAA AGCACCAGAC
    GGGCCAGAAA GCCCCGAGGG CAGCCCCCGC GGTTCAGAGG CCGCCACCGC CGCCGAGGCT
    CGGCTGAGCC TGCCCGCCGG TCCCTTCGTG CTGACCGAGC CAGAGGACGA GGTGGACATT
    GGAGACGAGG GGGAGCTGGG CTCAGGGCCG CACGTGCTCT GA

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

  • PubMed

    Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche.
    Nature514(7520)92-97(2014 Oct)
    Perry JR,Day F,Elks CE,Sulem P,Thompson DJ,Ferreira T,He C,Chasman DI,Esko T,Thorleifsson G,Albrecht E,Ang WQ,Corre T,Cousminer DL,Feenstra B,Franceschini N,Ganna A,Johnson AD,Kjellqvist S,Lunetta KL,McMahon G,Nolte IM,Paternoster L,Porcu E,Smith AV,Stolk L,Teumer A,T?ernikova N,Tikkanen E,Ulivi S,Wagner EK,Amin N,Bierut LJ,Byrne EM,Hottenga JJ,Koller DL,Mangino M,Pers TH,Yerges-Armstrong LM,Zhao JH,Andrulis IL,Anton-Culver H,Atsma F,Bandinelli S,Beckmann MW,Benitez J,Blomqvist C,Bojesen SE,Bolla MK,Bonanni B,Brauch H,Brenner H,Buring JE,Chang-Claude J,Chanock S,Chen J,Chenevix-Trench G,Coll?e JM,Couch FJ,Couper D,Coveillo AD,Cox A,Czene K,D'adamo AP,Smith GD,De Vivo I,Demerath EW,Dennis J,Devilee P,Dieffenbach AK,Dunning AM,Eiriksdottir G,Eriksson JG,Fasching PA,Ferrucci L,Flesch-Janys D,Flyger H,Foroud T,Franke L,Garcia ME,Garc?a-Closas M,Geller F,de Geus EE,Giles GG,Gudbjartsson DF,Gudnason V,Gu?nel P,Guo S,Hall P,Hamann U,Haring R,Hartman CA,Heath AC,Hofman A,Hooning MJ,Hopper JL,Hu FB,Hunter DJ,Karasik D,Kiel DP,Knight JA,Kosma VM,Kutalik Z,Lai S,Lambrechts D,Lindblom A,M?gi R,Magnusson PK,Mannermaa A,Martin NG,Masson G,McArdle PF,McArdle WL,Melbye M,Michailidou K,Mihailov E,Milani L,Milne RL,Nevanlinna H,Neven P,Nohr EA,Oldehinkel AJ,Oostra BA,Palotie A,Peacock M,Pedersen NL,Peterlongo P,Peto J,Pharoah PD,Postma DS,Pouta A,Pylk?s K,Radice P,Ring S,Rivadeneira F,Robino A,Rose LM,Rudolph A,Salomaa V,Sanna S,Schlessinger D,Schmidt MK,Southey MC,Sovio U,Stampfer MJ,St?ckl D,Storniolo AM,Timpson NJ,Tyrer J,Visser JA,Vollenweider P,V?lzke H,Waeber G,Waldenberger M,Wallaschofski H,Wang Q,Willemsen G,Winqvist R,Wolffenbuttel BH,Wright MJ,,,,,,,Boomsma DI,Econs MJ,Khaw KT,Loos RJ,McCarthy MI,Montgomery GW,Rice JP,Streeten EA,Thorsteinsdottir U,van Duijn CM,Alizadeh BZ,Bergmann S,Boerwinkle E,Boyd HA,Crisponi L,Gasparini P,Gieger C,Harris TB,Ingelsson E,J?rvelin MR,Kraft P,Lawlor D,Metspalu A,Pennell CE,Ridker PM,Snieder H,S?rensen TI,Spector TD,Strachan DP,Uitterlinden AG,Wareham NJ,Widen E,Zygmunt M,Murray A,Easton DF,Stefansson K,Murabito JM,Ong KK


    Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies.
    Nature genetics42(12)1077-85(2010 Dec)
    Elks CE,Perry JR,Sulem P,Chasman DI,Franceschini N,He C,Lunetta KL,Visser JA,Byrne EM,Cousminer DL,Gudbjartsson DF,Esko T,Feenstra B,Hottenga JJ,Koller DL,Kutalik Z,Lin P,Mangino M,Marongiu M,McArdle PF,Smith AV,Stolk L,van Wingerden SH,Zhao JH,Albrecht E,Corre T,Ingelsson E,Hayward C,Magnusson PK,Smith EN,Ulivi S,Warrington NM,Zgaga L,Alavere H,Amin N,Aspelund T,Bandinelli S,Barroso I,Berenson GS,Bergmann S,Blackburn H,Boerwinkle E,Buring JE,Busonero F,Campbell H,Chanock SJ,Chen W,Cornelis MC,Couper D,Coviello AD,d'Adamo P,de Faire U,de Geus EJ,Deloukas P,D?ring A,Smith GD,Easton DF,Eiriksdottir G,Emilsson V,Eriksson J,Ferrucci L,Folsom AR,Foroud T,Garcia M,Gasparini P,Geller F,Gieger C,,Gudnason V,Hall P,Hankinson SE,Ferreli L,Heath AC,Hernandez DG,Hofman A,Hu FB,Illig T,J?rvelin MR,Johnson AD,Karasik D,Khaw KT,Kiel DP,Kilpel?inen TO,Kolcic I,Kraft P,Launer LJ,Laven JS,Li S,Liu J,Levy D,Martin NG,McArdle WL,Melbye M,Mooser V,Murray JC,Murray SS,Nalls MA,Navarro P,Nelis M,Ness AR,Northstone K,Oostra BA,Peacock M,Palmer LJ,Palotie A,Par? G,Parker AN,Pedersen NL,Peltonen L,Pennell CE,Pharoah P,Polasek O,Plump AS,Pouta A,Porcu E,Rafnar T,Rice JP,Ring SM,Rivadeneira F,Rudan I,Sala C,Salomaa V,Sanna S,Schlessinger D,Schork NJ,Scuteri A,Segr? AV,Shuldiner AR,Soranzo N,Sovio U,Srinivasan SR,Strachan DP,Tammesoo ML,Tikkanen E,Toniolo D,Tsui K,Tryggvadottir L,Tyrer J,Uda M,van Dam RM,van Meurs JB,Vollenweider P,Waeber G,Wareham NJ,Waterworth DM,Weedon MN,Wichmann HE,Willemsen G,Wilson JF,Wright AF,Young L,Zhai G,Zhuang WV,Bierut LJ,Boomsma DI,Boyd HA,Crisponi L,Demerath EW,van Duijn CM,Econs MJ,Harris TB,Hunter DJ,Loos RJ,Metspalu A,Montgomery GW,Ridker PM,Spector TD,Streeten EA,Stefansson K,Thorsteinsdottir U,Uitterlinden AG,Widen E,Murabito JM,Ong KK,Murray A


    A census of human transcription factors: function, expression and evolution.
    Nature reviews. Genetics10(4)252-63(2009 04)
    Vaquerizas JM,Kummerfeld SK,Teichmann SA,Luscombe NM


    Chromosomal microarray mapping suggests a role for BSX and Neurogranin in neurocognitive and behavioral defects in the 11q terminal deletion disorder (Jacobsen syndrome).
    Neurogenetics10(2)89-95(2009 Apr)
    Coldren CD,Lai Z,Shragg P,Rossi E,Glidewell SC,Zuffardi O,Mattina T,Ivy DD,Curfs LM,Mattson SN,Riley EP,Treier M,Grossfeld PD


    Cloning and functional analysis of hypothalamic homeobox gene Bsx1a and its isoform, Bsx1b.
    Molecular and cellular biology27(10)3743-9(2007 May)
    Chu HY,Ohtoshi A