SNTG1 (NM_001287813) Human Untagged Clone
CAT#: SC336577
SNTG1 (untagged) - Human syntrophin, gamma 1 (SNTG1), transcript variant 2
CNY 5,040.00
货期*
4周
规格
Product images
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经常一起买 (4)
SNTG1 mouse monoclonal antibody, clone OTI3G10 (formerly 3G10)
CNY 1,999.00
CNY 2,700.00
Specifications
Product Data | |
Type | Human Untagged Clone |
Tag | Tag Free |
Synonyms | G1SYN; SYN4 |
Vector | pCMV6-Entry |
Sequence Data |
>SC336577 representing NM_001287813.
Blue=Insert sequence Red=Cloning site Green=Tag(s) ATGGATTTCAGAACCGCCTGTGAGGAGACAAAGACAGGAATTTGTTTGCTGCAGGATGGTAACCAGGAG CCTTTCAAAGTGCGGCTGCACCTAGCCAAAGACATTTTGATGATCCAGGAACAGGATGTGATATGTGTG TCTGGTGAGCCTTTCTATTCTGGTGAAAGAACGGTGACCATCAGAAGACAAACAGTAGGAGGATTTGGA TTAAGCATAAAGGGAGGAGCAGAACATAACATTCCAGTTGTCGTTTCAAAAATCTCCAAGGAACAAAGA GCGGAACTTTCAGGACTACTTTTTATTGGAGATGCAATTCTACAGATAAATGGCATTAATGTGAGAAAA TGTAGACATGAAGAAGTGGTTCAGGTTCTTCGGAATGCTGGAGAAGAAGTGACTCTAACAGTGTCATTT TTAAAAAGAGCACCTGCTTTCCTCAAACTCCCATTGAATGAAGATTGTGCATGTGCTCCAAGTGACCAG AGCAGTGGCACCTCCTCTCCTCTCTGTGACAGTGGCTTACATCTCAACTACCATCCCAACAATACAGAC ACATTATCATGCTCGTCGTGGCCGACGTCTCCAGGCTTGAGGTGGGAGAAGCGATGGTGCGACCTCAGA CTGATCCCTCTACTTCATTCGCGCTTCTCTCAGTATGTGCCCGGCACAGATTTGAGTCGGCAGAATGCC TTTCAAGTCATTGCTGTGGATGGGGTCTGCACTGGGATTATTCAGTGCCTCTCTGCTGAAGACTGCGTT GACTGGCTACAAGCAATAGCAACTAACATTTCAAATCTCACAAAGCACAATATTAAAAAAATCAACAGA AACTTTCCTGTAAACCAGCAGATTGTCTACATGGGCTGGTGTGAAGCCCGGGAGCAAGACCCCCTCCAG GACAGAGTGTACTCCCCGACCTTCCTGGCCCTGAGGGGCTCATGTCTCTACAAGTTTCTGGCACCTCCA GTGACCACCTGGGACTGGACGAGAGCAGAGAAAACATTCTCAGTTTATGAGATTATGTGCAAGATCCTC AAGGACAGTGACCTGCTGGACCGACGGAAACAGTGCTTCACCGTGCAGTCTGAGTCTGGGGAGGACCTG TACTTCTCAGTGGAGCTGGAAAGTGACCTCGCCCAGTGGGAAAGAGCCTTCCAGACAGCAACCTTTCTA GAAGTAGAACGGATACAGTGCAAGACCTATGCATGTGTGCTAGAAAGTCATCTAATGGGACTCACAATT GATTTCAGCACAGGATTTATCTGCTTTGATGCTGCAACAAAGGCTGTCCTTTGGAGGTATAAATTCTCT CAGCTTAAAGGTTCTTCAGATGATGGCAAGAGCAAAATCAAATTTTTGTTTCAGAATCCAGATACTAAA CAGATTGAAGCAAAGGAGTTGGAATTTTCTAATTTATTTGCTGTTCTTCACTGCATTCATTCCTTCTTT GCTGCCAAGGTAGCTTGTTTGGACCCTCTATTTTTAGGCAATCAAGCTACTGCTTCTACTGCTGCCAGC TCTGCTACCACGAGCAAAGCAAAGTATACAACTTGA |
Restriction Sites | SgfI-MluI |
ACCN | NM_001287813 |
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). |
Product 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 | 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. |
Reference Data | |
RefSeq | NM_001287813.1 |
RefSeq Size | 3214 bp |
RefSeq ORF | 1554 bp |
Locus ID | 54212 |
UniProt ID | Q9NSN8 |
MW | 58 kDa |
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 (2) differs in the 5' UTR compared to variant 1. Variants 1, 2 and 4 all encode 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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