Synaptotagmin 14 (SYT14) (NM_001256006) Human Untagged Clone
Product Data | |
Type | Human Untagged Clone |
---|---|
Target Symbol | Synaptotagmin 14 |
Synonyms | SCAR11; sytXIV |
Vector | pCMV6-Entry |
Sequence Data |
Fully Sequenced ORF
>SC330344 representing NM_001256006.
Blue=Insert sequence Red=Cloning site Green=Tag(s) ATGCTGCTCCTTTTTCTCTATATTAATAAGAAGTTCTGTTTTGAAAATGTTGGCGGGTTTCCAGATCTT GGTTCAGAATACAGTACAAGGAAGAATTCACAAGATAAAATTTATAATTCCTACATGGACAAAGATGAG CATGGTTCATCCTCTGAAAGTGAAGATGAAGCGCTGGGTAAATATCATGAGGCCTTATCCAGAACACAC AATTCCAGACTACCACTGGCAGATTCTAGACAAAGGAACTATGCTTGGGAAACAAGGCAGAAATACAGT CCTCTATCGGCAGAGTATGATGGATACAGTAGTGAAGCATCAATAGATGAAGGAAACTGCATTCAGAGA ATGAGAAGAACACCCCCGCTGGATGAATTGCAGCCACCACCATATCAGGATGACAGTGGTTCTCCCCAT CTGTCATGTACACCCTCAGAAATTGGGGACAGTAAATGTGAATTTTCCCACTGCAGCAACAGTCCAAGA TGCTCATATAACAAGTGCCCAAGTGAAGGAAGCACAGGTCATGAAATAGAAAGTTTTCATAATAAAGGA TATGAAGAAGATGTTCCAAGTGACAGCACTGCAGTCCTGAGCCCTGAAGATATGTCAGCTCAAGGATCA TCTTCGCAGCTTCCTAAACCTTTTGATCCTGAGCCAGAAGCTAAATATGGCACACTGGATGTGACTTTT GACTATGACTCACAAGAACAGAAGCTTCTGGTAACAGTGACAGCTGTCACAGACATCCCAACATATAAC AGGACAGGTGGCAACTCATGGCAAGTACACCTTGTTCTTCTACCTATAAAGAAACAGAGAGCAAAAACC AGCATCCAGAGAGGACCATGCCCTGTCTTCACAGAAACATTTAAATTTAATCATGTTGAATCTGAGATG ATTGGAAATTATGCAGTTCGGTTTAGACTGTATGGTGTACATCGCATGAAAAAAGAAAAGATTGTGGGG GAAAAGATTTTTTATTTAACAAAATTGAATCTTCAAGGGAAAATGTCATTGCCTGTGATATTGGAACCT TCTTACAATCATTCTGGCTGTGACTCCCAAATGAGCGTGTCAGAAATGTCGTGTAGTGAAAGTACATCC TCATGTCAGTCTCTTGAACATGGCTCAGTTCCAGAAATTCTTATTGGCCTGCTTTATAATGCCACAACT GGAAGACTATCAGCAGAAGTGATAAAAGGCAGCCACTTCAAAAATTTGGCAGCAAACAGACCACCCAAT ACATATGTTAAGTTAACTCTACTGAATTCCATGGGTCAAGAGATGTCCAAATGCAAGACATCCATCCGC AGAGGGCAGCCAAATCCAGTATATAAGGAAACTTTTGTCTTTCAAGTGGCCCTATTTCAGCTTTCTGAT GTGACACTCATACTGTCTGTGTATAACAAACGCAGCATGAAAAGAAAAGAGATGATAGGCTGGATTTCT TTAGGTCTCAACAGCTCTGGAGAAGAAGAACTCAATCACTGGACTGAAATGAAAGAGTCAAAAGGACAG CAAGTATGTAGATGGCATGCGTTGCTAGAGTCATGA |
Restriction Sites | SgfI-MluI |
ACCN | NM_001256006 |
Insert Size | 1554 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). |
Components | The ORF clone is ion-exchange column purified and shipped in a 2D barcoded Matrix tube containing 10ug of transfection-ready, dried plasmid DNA (reconstitute with 100 ul of water). |
Reconstitution Method | 1. Centrifuge at 5,000xg for 5min. 2. Carefully open the tube and add 100ul of sterile water to dissolve the DNA. 3. Close the tube and incubate for 10 minutes at room temperature. 4. Briefly vortex the tube and then do a quick spin (less than 5000xg) to concentrate the liquid at the bottom. 5. Store the suspended plasmid at -20°C. The DNA is stable for at least one year from date of shipping when stored at -20°C. |
Note | Plasmids are not sterile. For experiments where strict sterility is required, filtration with 0.22um filter is required. |
Shipping | Ambient |
Reference Data | |
RefSeq | NM_001256006.1 |
RefSeq Size | 5213 bp |
RefSeq ORF | 1554 bp |
Locus ID | 255928 |
UniProt ID | Q8NB59 |
Cytogenetics | 1q32.2 |
Protein Families | Transmembrane |
MW | 58.3 kDa |
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 (5) lacks two internal exons, contains an alternate internal exon in the 5' region, and initiates translation at a downstream, in-frame start codon, compared to variant 1. The encoded isoform (5) is shorter than 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. |
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