CBX2 (NM_032647) Human Untagged Clone

CAT#: SC123042

CBX2 (untagged)-Human chromobox homolog 2 (CBX2), transcript variant 2

Specifications

Product Data

• Type: Human Untagged Clone
• Tag: Tag Free
• Symbol: CBX2
• Synonyms: CDCA6; M33; SRXY5
• Vector: pCMV6-XL5
• E. coli Selection: Ampicillin (100 ug/mL)
• Mammalian Cell Selection: None
• Sequence Data:
  Fully Sequenced ORF

  >OriGene sequence for NM_032647 edited
  GACTGGCGGCGGGCGCCGCGGTCGGGCTGGCTGCCGGGCAGCATGGAGGAGCTGAGCAGC
  GTGGGCGAGCAGGTCTTCGCCGCCGAGTGCATCCTGAGCAAGCGGCTCCGCAAGGGCAAG
  CTGGAGTACCTGGTCAAGTGGCGCGGCTGGTCCTCCAAACATAACAGCTGGGAGCCGGAG
  GAGAACATCCTGGACCCGAGGCTGCTCCTGGCCTTCCAGAAGAAGGAACATGAGAAGGAG
  GTGCAGAACCGGAAGAGAGGCAAGAGGCCGAGAGGCCGGCCAAGGAAGCTCACTGCCATG
  TCCTCCTGCAGCCGGCGCTCCAAGCTCAAGGTGGGTGGCTGCGCTGGGTATGCTGACCCC
  ACCTCCCAGCACCCCCTTGGCGTAGGGGGCAGGCAGAGGGAGGGTTTGGGGCCCTCAGGA
  AGGGGGTGGCACTTCTGCCAACAGTCTGTCCCTCTACTCGGAAAACAGGAGCCCCCTTTC
  TTCCTGTCTCTCAGCTTCTGCTGCCAGGGGCCCCAGCCGGCTGAGAGTTCCTCCCCGCCC
  CTCCCAGGGGCTTCCTGCTTCAGCCTGTCCTGCACGCCTCTCTGCTGGGTGGCAGGGTCA
  AACTGCTGCAGACAAGCACTCTTCCCTCCCAGGGGGTCCTTGGGGGACGGAAAGGAACAG
  GAAGCATGCGTACAGTAGGTGCTCATAGGATTGCCGGCTGGATGTGACTCAAAAGCCTAA
  GATTTGGGGGCTACTCCGGGCCCACCTGCGGGTGCACCTTAAATCGAGGTGGCCACGAAA
  GGCAGGGCTGACTGAATAGCCAGGGGGTGCCAGGAGGGGCCTTGGAGGAGGGCAGAGGCA
  GTGTGGGCTGATGATGTGCTTTGGCCTTCTCGGGACTGTCCTGTCACCCCTCCTCGCTAC
  AGTGATGGGCTCACCCCGCCACAGGTATGCATGCGCCCCTGGGGTCCGTGGTAGGGCCCC
  TCCCTCCCCTGAGGACAGGTGAGGCAGGACAGGATGGGGGAGGAGGGCCTGGCCTCAGTC
  CCGGGTGTGGCTTTGATTCCCTCCTCCGGGCACTGTCCCTGATACAAAAAAAAAAAAAAA
  AAAAAAGAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAC
  
  5' Read Nucleotide Sequence

  >OriGene 5' read for NM_032647 unedited
  NGGAAGCGTCAAAATTGTATACGACTCATATAGGCGGCCGCGNAATTCGCACGAGGGACT
  GGCGGCGGGCGCCGCGGTCGGGCTGGCTGCCGGGCAGCATGGAGGAGCTGAGCAGCGTGG
  GCGAGCAGGTCTTCGCCGCCGAGTGCATCCTGAGCAAGCGGCTCCGCAAGGGCAAGCTGG
  AGTACCTGGTCAAGTGGCGCGGCTGGTCCTCCAAACATAACAGCTGGGAGCCGGAGGAGA
  ACATCCTGGACCCGAGGCTGCTCCTGGCCTTCCAGAAGAAGGAACATGAGAAGGAGGTGC
  AGAACCGGAAGAGAGGCAAGAGGCCGAGAGGCCGGCCAAGGAAGCTCACTGCCATGTCCT
  CCTGCAGCCGGCGCTCCAAGCTCAAGGTGGGTGGCTGCGCTGGGTATGCTGACCCCACCT
  CCCAGCACCCCCTTGGCGTAGGGGGCAGGCAGAGGGAGGGTTTGGGGCCCTCAGGAAGGG
  GGTGGCACTTCTGCCAACAGTCTGTCCCTCTACTCGGAAAACAGGAGCCCCCTTTCTTCC
  TGTCTCTCAGCTTCTGCTGCCAGGGGCCCCAGCCGGCTGAGAGTTCCTCCCCGCCCCTCC
  CGGGGCTTCCTGCTTCAGCCTGTCCTGCACGCCTCTCTGCTGGGTGGCAGGGTCAAACTG
  CTGCAGACAAGCACTCTTCCCTCCCAGGGGGTCCTTGGGGGACGGAAAGGAACAGGAAGC
  ATGCGTACAGTAGGTGCTCATAGGATTGCCGGCTGGATGTGACTCANAAGCCTAAGATTT
  GGGGGCTACTCCGGGCCCACCTGCGGGTGCACCTTANATCGAGGTGGCCACGAAAGGCAG
  GGCTGACTGAATAGCCAGGGGGTGCCAGGAGGGGCCTTGGAGGAAGGCAGAGCAGTGTGG
  CCT
  
• Restriction Sites: Please inquire
• ACCN: NM_032647
• ORF Size: 636 bp
• Insert Size: 1131
• 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_032647.2, NP_116036.1
• RefSeq Size: 1061
• RefSeq ORF: 636
• Locus ID: 84733
• Protein Families: Transcription Factors
• Gene Summary: This gene encodes a component of the polycomb multiprotein complex, which is required to maintain the transcriptionally repressive state of many genes throughout development via chromatin remodeling and modification of histones. Disruption of this gene in mice results in male-to-female gonadal sex reversal. Mutations in this gene are also associated with gonadal dysgenesis in humans. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene. [provided by RefSeq, Mar 2010]
  Transcript Variant: This variant (2) lacks a 3' exon compared to variant 1, resulting in an alternate 3' coding region and UTR. It encodes a shorter isoform (2) with an unique C-terminus compared to isoform 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.