SNTG1 (NM_001287814) Human Untagged Clone

CAT#: SC336373

SNTG1 (untagged) - Human syntrophin, gamma 1 (SNTG1), transcript variant 3

Specifications

Product Data

• Type: Human Untagged Clone
• Tag: Tag Free
• Symbol: SNTG1
• Synonyms: G1SYN; SYN4
• Vector: pCMV6-Entry
• E. coli Selection: Kanamycin (25 ug/mL)
• Mammalian Cell Selection: Neomycin
• Sequence Data:
  Fully Sequenced ORF

  >NCBI ORF sequence for NM_001287814, the custom clone sequence may differ by one or more nucleotides
  
  
  ATGGATTTCAGAACCGCCTGTGAGGAGACAAAGACAGGAATTTGTTTGCTGCAGGATGGTAACCAGGAGC
  CTTTCAAAGTGCGGCTGCACCTAGCCAAAGACATTTTGATGATCCAGGAACAGGATGTGATATGTGTGTC
  TGGTGAGCCTTTCTATTCTGGTGAAAGAACGGTGACCATCAGAAGACAAACAGTAGGAGGATTTGGATTA
  AGCATAAAGGGAGGAGCAGAACATAACATTCCAGTTGTCGTTTCAAAAATCTCCAAGGAACAAAGAGCGG
  AACTTTCAGGACTACTTTTTATTGGAGATGCAATTCTACAGATAAATGGCATTAATGTGAGAAAATGTAG
  ACATGAAGAAGTGGTTCAGGTTCTTCGGAATGCTGGAGAAGAAGTGACTCTAACAGTGTCATTTTTAAAA
  AGAGCACCTGCTTTCCTCAAACTCCCATTGAATGAAGATTGTGCATGTGCTCCAAGTGACCAGAGCAGTG
  GCACCTCCTCTCCTCTCTGTGACAGTGGCTTACATCTCAACTACCATCCCAACAATACAGACACATTATC
  ATGCTCGTCGTGGCCGACGTCTCCAGGCTTGAGGTGGGAGAAGCGATGGTGCGACCTCAGACTGATCCCT
  CTACTTCATTCGCGCTTCTCTCAGTATGTGCCCGGCACAGATTTGAGTCGGCAGAATGCCTTTCAAGTCA
  TTGCTGTGGATGGGGTCTGCACTGGGATTATTCAGTGCCTCTCTGCTGAAGACTGCGTTGACTGGCTACA
  AGCAATAGCAACTAACATTTCAAATCTCACAAAGCACAATATTAAAAAAATCAACAGAAACTTTCCTGTA
  AACCAGCAGATTGTCTACATGGGCTGGTGTGAAGCCCGGGAGCAAGACCCCCTCCAGGACAGAGTGTACT
  CCCCGACCTTCCTGGCCCTGAGGGGCTCATGTCTCTACAAGTTTCTGGCACCTCCAGTGACCACCTGGGA
  CTGGACGAGAGCAGAGAAAACATTCTCAGTTTATGAGATTATGTGCAAGATCCTCAAGGACAGTGACCTG
  CTGGACCGACGGAAACAGTGCTTCACCGTGCAGTCTGAGTCTGGGGAGGACCTGTACTTCTCAGTGGAGC
  TGGAAAGTGACCTCGCCCAGTGGGAAAGAGCCTTCCAGACAGCAACCTTTCTAGAAGTAGAACGGATACA
  GTGCAAGACCTATGCATGTGTGCTAGAAAGTCATCTAATGGGACTCACAATTGATTTCAGCACAGGATTT
  ATCTGCTTTGATGCTGCAACAAAGGAGTTGGAATTTTCTAATTTATTTGCTGTTCTTCACTGCATTCATT
  CCTTCTTTGCTGCCAAGGTAGCTTGTTTGGACCCTCTATTTTTAGGCAATCAAGCTACTGCTTCTACTGC
  TGCCAGCTCTGCTACCACGAGCAAAGCAAAGTATACAACTTGA
  
  
• Restriction Sites: SgfI-MluI
• ACCN: NM_001287814
• ORF Size: 1443 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_001287814.2, NP_001274743.1
• RefSeq Size: 5856
• RefSeq ORF: 1443
• Locus ID: 54212
• Gene Summary: The protein encoded by this gene is a member of the syntrophin family. Syntrophins are cytoplasmic peripheral membrane proteins that typically contain 2 pleckstrin homology (PH) domains, a PDZ domain that bisects the first PH domain, and a C-terminal domain that mediates dystrophin binding. This family member plays a role in mediating gamma-enolase trafficking to the plasma membrane and in enhancing its neurotrophic activity. Mutations in this gene are associated with idiopathic scoliosis. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Mar 2016]
  Transcript Variant: This variant (3) lacks a 5' non-coding exon and an in-frame penultimate coding exon compared to variant 1. The resulting shorter isoform (2) lacks an internal protein segment in the C-terminal region 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.