Synaptotagmin 14 (SYT14) (NM_001146261) Human Untagged Clone

CAT#: SC327611

SYT14 (untagged)-Human synaptotagmin XIV (SYT14) transcript variant 1

Specifications

Product Data

• Type: Human Untagged Clone
• Tag: Tag Free
• Symbol: SYT14
• Synonyms: SCAR11; sytXIV
• Vector: pCMV6-XL5
• E. coli Selection: Ampicillin (100 ug/mL)
• Mammalian Cell Selection: None
• Sequence Data:
  Fully Sequenced ORF

  >NCBI ORF sequence for NM_001146261, the custom clone sequence may differ by one or more nucleotides
  ATGGCGAGCGCATCATGGCGATTGAAGGTGGAGAGAGAACCTGTGGAGTACATGAACTTA
  TCTGTATTAGAAAAGATAGGGTATTTCTCTGTGGCCAGGCTGGAGTACAGTGGCACCATC
  TTGGCTCACTGCAACTTCCGCCTCCTGGGTTCAAACGATTCTTCTGCCTCAGCATCCCAA
  GTAACTGGGACTACAGTATCTCCAGAGGCAGTTGGATTTTTGTCAGCTGTTGGGGTGTTT
  ATTATCTTGATGCTGCTCCTTTTTCTCTATATTAATAAGAAGTTCTGTTTTGAAAATGTT
  GGCGGGTTTCCAGATCTTGGTTCAGAATACAGTACAAGGAAGAATTCACAAGATAAAATT
  TATAATTCCTACATGGACAAAGATGAGCATGGTTCATCCTCTGAAAGTGAAGATGAAGCG
  CTGGGTAAATATCATGAGGCCTTATCCAGAACACACAATTCCAGACTACCACTGGCAGAT
  TCTAGACAAAGGAACTATGCTTGGGAAACAAGGCAGAAATACAGTCCTCTATCGGCAGAG
  TATGATGGATACAGTAGTGAAGCATCAATAGATGAAGGAAACTGCATTCAGAGAATGAGA
  AGAACACCCCCGCTGGATGAATTGCAGCCACCACCATATCAGGATGACAGTGGTTCTCCC
  CATCTGTCATGTACACCCTCAGAAATTGGGGACAGTAAATGTGAATTTTCCCACTGCAGC
  AACAGTCCAAGATGCTCATATAACAAGTGCCCAAGTGAAGGAAGCACAGGTCATGAAATA
  GAAAGTTTTCATAATAAAGGATATGAAGAAGATGTTCCAAGTGACAGCACTGCAGTCCTG
  AGCCCTGAAGATATGTCAGCTCAAGGATCATCTTCGCAGCTTCCTAAACCTTTTGATCCT
  GAGCCAGAAGCTAAATATGGCACACTGGATGTGACTTTTGACTATGACTCACAAGAACAG
  AAGCTTCTGGTAACAGTGACAGCTGTCACAGACATCCCAACATATAACAGGACAGGTGGC
  AACTCATGGCAAGTACACCTTGTTCTTCTACCTATAAAGAAACAGAGAGCAAAAACCAGC
  ATCCAGAGAGGACCATGCCCTGTCTTCACAGAAACATTTAAATTTAATCATGTTGAATCT
  GAGATGATTGGAAATTATGCAGTTCGGTTTAGACTGTATGGTGTACATCGCATGAAAAAA
  GAAAAGATTGTGGGGGAAAAGATTTTTTATTTAACAAAATTGAATCTTCAAGGGAAAATG
  TCATTGCCTGTGATATTGGAACCTTCTTACAATCATTCTGGCTGTGACTCCCAAATGAGC
  GTGTCAGAAATGTCGTGTAGTGAAAGTACATCCTCATGTCAGTCTCTTGAACATGGCTCA
  GTTCCAGAAATTCTTATTGGCCTGCTTTATAATGCCACAACTGGAAGACTATCAGCAGAA
  GTGATAAAAGGCAGCCACTTCAAAAATTTGGCAGCAAACAGACCACCCAATGGACTGTTC
  TGTTGTCTAAAACACTTGATAGGTGGACAGGTTTATATAATCCGAGATACATATGTTAAG
  TTAACTCTACTGAATTCCATGGGTCAAGAGATGTCCAAATGCAAGACATCCATCCGCAGA
  GGGCAGCCAAATCCAGTATATAAGGAAACTTTTGTCTTTCAAGTGGCCCTATTTCAGCTT
  TCTGATGTGACACTCATACTGTCTGTGTATAACAAACGCAGCATGAAAAGAAAAGAGATG
  ATAGGCTGGATTTCTTTAGGTCTCAACAGCTCTGGAGAAGAAGAACTCAATCACTGGACT
  GAAATGAAAGAGTCAAAAGGACAGCAAGTATGTAGATGGCATGCGTTGCTAGAGTCA
  
• Restriction Sites: Please inquire
• ACCN: NM_001146261
• ORF Size: 1860 bp
• Insert Size: 5186
• 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: This TrueClone is provided through our Custom Cloning Process that includes sub-cloning into OriGene's pCMV6 vector and full sequencing to provide a non-variant match to the expected reference without frameshifts, and is delivered as lyophilized plasmid DNA.

Reference Data

• RefSeq: NM_001146261.1, NP_001139733.1
• RefSeq Size: 5186
• RefSeq ORF: 1860
• Locus ID: 255928
• Protein Families: Transmembrane
• Gene Summary: This gene is a member of the synaptotagmin gene family and encodes a protein similar to other family members that mediate membrane trafficking in synaptic transmission. The encoded protein is a calcium-independent synaptotagmin. Mutations in this gene are a cause of autosomal recessive spinocerebellar ataxia-11 (SCAR11), and a t(1;3) translocation of this gene has been associated with neurodevelopmental abnormalities. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene, and a pseudogene of this gene is located on the long arm of chromosome 4. [provided by RefSeq, Dec 2011]
  Transcript Variant: This variant (1) encodes the longest 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.