HAX1 (NM_001018837) Human Untagged Clone

CAT#: SC302205

HAX1 (untagged)-Human HCLS1 associated protein X-1 (HAX1), transcript variant 2

Specifications

Product Data

• Type: Human Untagged Clone
• Tag: Tag Free
• Symbol: HAX1
• Synonyms: HCLSBP1; HS1BP1; SCN3
• Vector: pCMV6-XL5
• E. coli Selection: Ampicillin (100 ug/mL)
• Mammalian Cell Selection: None
• Sequence Data:
  Fully Sequenced ORF

  >OriGene sequence for NM_001018837 edited
  CACATTCTGACCCCCCATCAGCAGCCGCATTCTCAGATCCTTCACCATCACCTGCAGCAG
  GATGGCCAGGGCTGCGCAGGTTGCCCCCGTCTGCGAATGGACCACTGGAGGGGTTCAAAG
  GTTCGCGTCCCAGTACGGGAATGAGCCTCTTTGATCTCTTCCGGGGCTTTTTCGGCTTTC
  CTGGACCTCGGAGCTTCAGCCCAGGAGGAGGGATACGTTTCCACGATAACTTCGGCTTTG
  ATGACCTAGTACGAGATTTCAATAGCATCTTCAGCGATATGGGGGCCTGGACCTTGCCTT
  CCCATCCTCCTGAACTTCCAGGTCCTGAGTCAGAGACACCTGGTGAGAGACTACGGGAGG
  GACAGACACTTCGGGACTCAATGCTTAAGTATCCAGATAGTCACCAGCCCAGGATCTTTG
  GGGGGGTCTTGGAGAGTGATGCAAGAAGTGAATCCCCCCAACCAGCACCAGACTGGGGCT
  CCCAGAGGCCATTTCATAGGTTTGATGATGTATGGCCTATGGACCCCCATCCTAGAACCA
  GAGAGGACAATGATCTTGATTCCCAGGTTTCCCAGGAGGGTCTTGGCCCGGTTCTACAGC
  CCCAGCCCAAATCCTATTTCAAGAGCATCTCTGTGACCAAGATCACTAAACCAGATGGGA
  TAGTGGAGGAGCGCCGGACTGTGGTGGACAGTGAGGGCCGGACAGAGACTACAGTAACCC
  GACACGAAGCAGATAGCAGTCCTAGGGGTGATCCAGAATCACCAAGACCTCCAGCCCTGG
  ATGATGCCTTTTCCATCCTGGACTTATTCCTGGGACGTTGGTTCCGGTCCCGGTAGCCTT
  GTTAACCCTCAGAGGCCTTCAAGTCCTTTCCACCTTTCACCCATTGCCCACCATTAATAA
  GCTTAGCTTCTCTTGCCACCTCAGGGGCTTGGATATGTGGAATAGTGAACTGGGGCCATG
  TCAGTTTGTCACTCACCCAAACTGACCAATAAAACCTTTATTTATGCTAAAAAAAAAAAA
  AAAAAAAAAAAAAAAAAAAAAAAAAAA
  
  5' Read Nucleotide Sequence

  >OriGene 5' read for NM_001018837 unedited
  NTTTTGGGGAAGGTCAGAATTTGTATACGACTCATATAGGGCGGCCGCGAATTCGCACCA
  GCACATTCTGACCCCCCATCAGCAGCCGCATTCTCAGATCCTTCACCATCACCTGCAGCA
  GGATGGCCAGGGCTGCGCAGGTTGCCCCCGTCTGCGAATGGACCACTGGAGGGGTTCAAA
  GGTTCGCGTCCCAGTACGGGAATGAGCCTCTTTGATCTCTTCCGGGGCTTTTTCGGCTTT
  CCTGGACCTCGGAGCTTCAGCCCAGGAGGAGGGATACGTTTCCACGATAACTTCGGCTTT
  GATGACCTAGTACGAGATTTCAATAGCATCTTCAGCGATATGGGGGCCTGGACCTTGCCT
  TCCCATCCTCCTGAACTTCCAGGTCCTGAGTCAGAGACACCTGGTGAGAGACTACGGGAG
  GGACAGACACTTCGGGACTCAATGCTTAAGTATCCAGATAGTCACCAGCCCAGGATCTTT
  GGGGGGGTCTTGGAGAGTGATGCAAGAAGTGAATCCCCCCAACCAGCACCAGACTGGGGC
  TCCCAGAGGCCATTTCATAGGTTTGATGATGTATGGCCTATGGACCCCCATCCTAGAACC
  AGAGAGGACAATGATCTTGATTCCCAGGTTTCCCAGGAGGGTCTTGGCCCGGTTCTACAG
  CCCCAGCCCAAATCCTATTTCAAGAGCATCTCTGTGACCAAGATCACTAAACCAGATGGG
  ATAGTGGAGGAGCGCCGGACTGTGGTGGACAGTGAGGGCCGGACAGAGACTACAGTAACC
  CGACACGAAGCAGATAGCAGTCCTAGGGGTGATCCCAGATCACCAAGACCTCCAGCCCTG
  GATGATGCTTTTNCATCCTGNACTTATTNCTGGACGTTGNTCCCGTCCCNGTAGCTT
  
• Restriction Sites: Please inquire
• ACCN: NM_001018837
• ORF Size: 696 bp
• Insert Size: 1000
• 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).
• OTI Annotation: The open reading frame of this TrueClone was fully sequenced and found to be a perfect match to the protein associated to this reference.

Reference Data

• RefSeq: NM_001018837.1, NP_001018238.1
• RefSeq Size: 1052
• RefSeq ORF: 696
• Locus ID: 10456
• Gene Summary: The protein encoded by this gene is known to associate with hematopoietic cell-specific Lyn substrate 1, a substrate of Src family tyrosine kinases. It also interacts with the product of the polycystic kidney disease 2 gene, mutations in which are associated with autosomal-dominant polycystic kidney disease, and with the F-actin-binding protein, cortactin. It was earlier thought that this gene product is mainly localized in the mitochondria, however, recent studies indicate it to be localized in the cell body. Mutations in this gene result in autosomal recessive severe congenital neutropenia, also known as Kostmann disease. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
  Transcript Variant: This variant (2) uses an alternate in-frame splice site compared to variant 1. The resulting isoform (b) has the same N- and C-termini but is shorter compared to isoform a.