TXNL4A (NM_006701) Human Untagged Clone

CAT#: SC115962

TXNL4A (untagged)-Human thioredoxin-like 4A (TXNL4A)

Specifications

Product Data

• Type: Human Untagged Clone
• Tag: Tag Free
• Symbol: TXNL4A
• Synonyms: BMKS; DIB1; DIM1; SNRNP15; TXNL4; U5-15kD
• Vector: pCMV6-XL5
• E. coli Selection: Ampicillin (100 ug/mL)
• Mammalian Cell Selection: None
• Sequence Data:
  Fully Sequenced ORF

  >OriGene ORF sequence for NM_006701 edited
  ATGTCGTACATGCTCCCGCACCTGCACAACGGCTGGCAGGTGGACCAGGCCATCCTCTCG
  GAGGAGGACCGCGTGGTCGTCATCCGCTTCGGCCACGACTGGGATCCTACGTGCATGAAG
  ATGGACGAGGTCCTGTACAGCATCGCCGAGAAGGTTAAAAATTTTGCAGTTATTTATCTT
  GTGGATATTACAGAAGTGCCTGACTTCAACAAAATGTATGAGTTATACGATCCATGTACT
  GTCATGTTTTTCTTCAGGAACAAGCACATCATGATTGACTTGGGGACTGGCAACAACAAC
  AAGATTAACTGGGCCATGGAGGACAAGCAGGAGATGGTGGACATCATCGAGACGGTGTAC
  CGCGGGGCCCGCAAAGGCCGCGGCCTGGTGGTGTCCCCCAAGGACTACTCCACCAAGTAC
  CGCTACTGA
  
  5' Read Nucleotide Sequence

  >OriGene 5' read for NM_006701 unedited
  CCGTCGGAATTGAAAACGATGCCTATAGGCGGCCGCGNAATTCGCACGAGGCGGGACCGG
  ATTTCGTCCGTGGGCCCGGGGGCGGCGGGGGCCGGGGAGTGAGGGGCCGGCTGAGCCCAC
  CTCGCTGGGCCCTCCCTGGCGCCCCGCCTTGGGCGGCGGCGAGCGCGCGGGCCGCCATGT
  CGTACATGCTCCCGCACCTGCACAACGGCTGGCAGGTGGACCAGGCCATCCTCTCGGAGG
  AGGACCGCGTGGTCGTCATCCGCTTCGGCCACGACTGGGATCCTACGTGCATGAAGATGG
  ACGAGGTCCTGTACAGCATCGCCGAGAAGGTTAAAAATTTTGCAGTTATTTATCTTGTGG
  ATATTACAGAAGTGCCTGACTTCAACAAAATGTATGAGTTATACGATCCATGTACTGTCA
  TGTTTTTCTTCAGGAACAAGCACATCATGATTGACTTGGGGACTGGCAACAACAACAAGA
  TTAACTGGGCCATGGAGGACAAGCAGGAGATGGTGGACATCATCGAGACGGTGTACCGCG
  GGGCCCGCAAAGGCCGCGGCCTGGTGGTGTCCCCCAAGGACTACTCCACCAAGTACCGCT
  ACTGAGGCGCCCTCAGTCTGCGCGGATAAATGTCGTGGAGCCCTTTTTGTATGGAAACGT
  TTTAAGCTATTTAAAGCCTTTGGAAAATACAGGAAGCTCCAGGGCTGGAGCACCTCTGAG
  ATGGAATTGATAACATGGTCTTAACTCNACCGAATAAACAAGCACGTGGTGAGAGGAAAA
  AAAAAAAAAAAAAACTCGACTCTAGATTGCGGCCGCGGCCATACCTGTTTCCTGAACAGA
  TCCCGGGTGGCATCCCTGTGACCCCNCCCCATGCCTCTCCTGCCCTGGA
  
  3' Read Nucleotide Sequence

  >OriGene 3' read for NM_006701 unedited
  CTAGAGTCGAGTTTTTTTTTTTTTTTTTTCCTCTCACACGTGCTTGTTTATTTCGGTGAG
  TTAAGACCATGTTATCAATTCCATCTCAGAGGTGCTCCACCCCTGGAGCTTCCTGTATTT
  TCCAAAGGCTTTAAATAGCTTAAAACGTTTCCATACAAAAAGGGCTCCACGACATTTATC
  CGTGCAGACTGAGGGCGCCTCAGTAGCGGTACTTGGTGGAGTAGTCCTTGGGGGACACCA
  CCAGGCCGCGGCCTTTGCGGCCCCCGTGGCACACCCGTTCGATGATGTCCACCATCTCCT
  GCTTGTCCTCCATGGACCACTCAATCTTGTTGCTGTTGCCAGTCCCCAAGTCAATCATGA
  TGCGCTTGTTCCTGATAAAAACTTGACAGTACATGGATCCTATACCTCATACATTTTGTT
  GAACCCAGGCACTTCTGTAATATCCACAAGATAAATAACTGCAAAACTTTTAACCTTCTC
  CGCGATGCTGTACAGGACCTCCTTCCATTTTCATGTCATCTCCCATCCCCCCTTCTGACT
  TCCATGTTTTCACCACCCACCCCGTTCCACCTCCCAAAAGCACGGCCNTGCCTCATCTCC
  CCCCCTCTCCCTATTTGTGCCGTGCACTTTCCCCCACACGGCCGGTAACCCCTCCCTATC
  CTCCATTACGCCCGCGTTCCATGCCGCCATTCCCCCCCGTGGATTTCCCCCCCATTCCCT
  TTTCCCCACCTTCTTCCACCTCTCCATACCCATATTCCTTCCTCCGTCCCCTTCCTTTCC
  ACCCTCCTTCCCTTCTTTTTACCCCACACCTCCTCCCTCACTCCCTCCATCCCTTCCTTC
  CGCGTCTCCCATTCCTACCATCCCTTCCCTATCCTACTTCACGTTTTTCTCCTTTCACCC
  CCCATCTATTATTTTTTCCTCACCTTATCGTCCCCGCGCATTCTCCATTCACCACCCGTT
  CCTTTCCCGCCTCCTTCTCCTTCTTCCTCCTTACCCCTTCCCCACACATCGCCTTCNTCC
  CCCGTTACTTCTCCCCACATATCTCCGCCACTTTTTCCTTCCCCCCGCCGCATCN
  
• Restriction Sites: NotI-NotI
• ACCN: NM_006701
• ORF Size: 429 bp
• Insert Size: 700
• 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_006701.2, NP_006692.1
• RefSeq Size: 1415
• RefSeq ORF: 429
• Locus ID: 10907
• Domains: DIM1
• Protein Families: Druggable Genome
• Protein Pathways: Spliceosome
• Gene Summary: The protein encoded by this gene is a member of the U5 small ribonucleoprotein particle (snRNP), and is involved in pre-mRNA splicing. This protein contains a thioredoxin-like fold and it is expected to interact with multiple proteins. Protein-protein interactions have been observed with the polyglutamine tract-binding protein 1 (PQBP1). Mutations in both the coding region and promoter region of this gene have been associated with Burn-McKeown syndrome, which is a rare disorder characterized by craniofacial dysmorphisms, cardiac defects, hearing loss, and bilateral choanal atresia. A pseudogene of this gene is found on chromosome 2. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2015]
  Transcript Variant: This variant (1) encodes the longest isoform (1).