BRRN1 (NCAPH) (NM_001281711) Human Untagged Clone

CAT#: SC337289

NCAPH (untagged) - Human non-SMC condensin I complex, subunit H (NCAPH), transcript variant 3


  "NM_001281711" in other vectors (1)

Reconstitution Protocol

USD 730.00

3 Weeks*

Size
    • 10 ug

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Specifications

Product Data
Type Human Untagged Clone
Tag Tag Free
Symbol NCAPH
Synonyms BRRN1; CAP-H; CAPH; MCPH23
Vector pCMV6-Entry
E. coli Selection Kanamycin (25 ug/mL)
Mammalian Cell Selection Neomycin
Sequence Data
>NCBI ORF sequence for NM_001281711, the custom clone sequence may differ by one or more nucleotides


ATGGGACCTCCCGGCCCAGAGCGTGTGTTCCCGATGCCCCTGCCCAGGAAGGCGCCTCTCAATATTCCTG
GCACCCCAGTCCTCGAAGACTTTCCTCAGAATGACGATGAGAAGGAGCGGCTGCAGCGGAGGCGCTCGAG
GGTCTTTGATCTGCAGTTCAGCACTGACTCACCTCGCTTATTGGCCTCCCCCTCCAGCAGGAGTATTGAC
ATTTCAGCTACTATCCCCAAGTTTACAAACACGCAGATTACGGAACATTACTCCACCTGTATCAAACTGT
CCACTGAAAATAAAATCACTACCAAGAATGCTTTTGGTTTGCACTTGATTGATTTTATGTCAGAGATTCT
TAAACAGAAAGACACCGAACCAACCAACTTTAAAGTGGCTGCGGGTACTCTGGATGCCAGCACCAAGATC
TATGCTGTGCGCGTGGATGCCGTCCATGCCGATGTATACAGAGTCCTTGGGGGGCTGGGCAAAGATGCAC
CGTCTTTGGAAGAAGTAGAAGGCCATGTTGCTGATGGAAGTGCTACTGAAATGGGAACAACCAAAAAGGC
TGTAAAGCCAAAGAAGAAGCACTTACACAGAACTATTGAGCAGAACATAAACAACCTCAATGTCTCCGAA
GCAGATCGGAAGTGTGAGATTGATCCCATGTTTCAGAAGACAGCAGCCTCATTTGATGAGTGCAGCACAG
CAGGGGTGTTTCTGTCCACTCTCCACTGCCAGGACTACAGAAGTGAACTGCTGTTTCCCTCTGATGTCCA
GACTCTCTCCACGGGAGAACCTCTCGAGTTGCCAGAGTTAGGTTGTGTAGAAATGACAGATTTAAAAGCG
CCCTTGCAGCAGTGTGCAGAAGATCGCCAGATCTGCCCTTCCCTGGCCGGGTTCCAGTTTACACAGTGGG
ACAGTGAAACACATAATGAGTCTGTGTCGGCCCTGGTAGACAAGTTTAAGAAGAATGACCAGGTATTTGA
CATCAATGCTGAAGTTGACGAGAGTGACTGTGGAGACTTCCCCGATGGGTCCCTGGGGGATGACTTTGAT
GCCAACGATGAACCTGACCACACCGCAGTTGGGGATCATGAAGAGTTCAGGAGCTGGAAGGAGCCCTGCC
AGGTTCAGAGCTGCCAGGAAGAAATGATTTCCCTTGGGGATGGAGACATCAGGACCATGTGCCCCCTTCT
GTCTATGAAACCTGGAGAATATTCTTATTTCAGTCCTCGGACCATGTCGATGTGGGCTGGCCCGGATCAC
TGGCGCTTTAGGCCTCGACGCAAACAAGATGCTCCTTCCCAATCAGAAAACAAAAAGAAGAGTACAAAAA
AAGATTTTGAAATTGACTTTGAAGATGATATTGACTTTGATGTATATTTTAGAAAAACAAAGGCTGCTAC
TATTCTGACCAAGTCCACTTTGGAGAACCAGAATTGGAGAGCTACCACCCTTCCTACAGATTTCAACTAC
AATGTTGACACTCTGGTCCAGCTTCACCTCAAACCAGGCACCAGGTTACTTAAGATGGCCCAGGGCCATA
GGGTAGAGACTGAGCATTATGAAGAAATTGAAGACTATGATTACAACAACCCTAACGACACCTCCAACTT
TTGCCCTGGATTACAGGCTGCTGACAGTGATGATGAAGATTTGGATGACTTATTTGTGGGACCTGTTGGG
AACTCTGACCTCTCACCTTATCCTTGCCATCCACCTAAGACAGCACAACAGAATGGTGACACTCCAGAAG
CCCAAGGATTAGACATCACAACATATGGGGAGTCAAACTTGGTAGCTGAGCCTCAGAAGGTAAATAAAAT
TGAAATTCACTATGCCAAGACTGCCAAAAAGATGGACATGAAGAAACTGAAGCAGAGCATGTGGAGTCTG
CTGACAGCGCTCTCCGGAAAGGAGGCAGATGCAGAGGCAAACCACAGGGAAGCTGGAAAAGAAGCGGCCC
TGGCAGAAGTGGCTGACGAGAAGATGCTTAGCGGGCTCACGAAGGACCTGCAGAGGAGCCTGCCCCCTGT
CATGGCTCAGAACCTCTCCATACCTCTGGCTTTTGCCTGTCTCCTACATTTAGCCAATGAAAAGAATCTA
AAACTGGAAGGAACAGAGGACCTCTCTGATGTTCTTGTGAGGCAAGGAGATTGA


Restriction Sites SgfI-MluI     
ACCN NM_001281711
ORF Size 2154 bp
OTI Disclaimer Our molecular clone sequence data has been matched to the reference identifier above as a point of reference. Note that the complete sequence of our molecular clones may differ from the sequence published for this corresponding reference, e.g., by representing an alternative RNA splicing form or single nucleotide polymorphism (SNP).
Reference Data
RefSeq NM_001281711.1, NP_001268640.1
RefSeq Size 5987
RefSeq ORF 2154
Locus ID 23397
Gene Summary This gene encodes a member of the barr gene family and a regulatory subunit of the condensin complex. This complex is required for the conversion of interphase chromatin into condensed chromosomes. The protein encoded by this gene is associated with mitotic chromosomes, except during the early phase of chromosome condensation. During interphase, the protein has a distinct punctate nucleolar localization. Alternatively spliced transcript variants encoding different proteins have been described. [provided by RefSeq, Jul 2013]
Transcript Variant: This variant (3) uses an alternate splice site in the 5' coding region compared to variant 1. The resulting protein (isoform 3) is shorter but has the same N- and C-termini 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.

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