Syntenin (SDCBP) (NM_005625) Human Tagged ORF Clone Lentiviral Particle

SKU
RC215390L3V
Lenti ORF particles, SDCBP (Myc-DDK tagged) - Human syndecan binding protein (syntenin) (SDCBP), transcript variant 1, 200ul, >10^7 TU/mL
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    Expression-ready ORF plasmid in lenti backbone

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$850.00
5 Weeks*
Specifications
Product Data
Type Human Tagged ORF Clone Lentiviral Particle
Tag Myc-DDK
Target Symbol Syntenin
Synonyms MDA-9; MDA9; ST1; SYCL; TACIP18
Vector pLenti-C-Myc-DDK-P2A-Puro
Mammalian Cell Selection Puromycin
Sequence Data
ORF Nucleotide Sequence
The ORF insert of this clone is exactly the same as(RC215390).
ACCN NM_005625
ORF Size 894 bp
OTI Disclaimer The molecular sequence of this clone aligns with the gene accession number as a point of reference only. However, individual transcript sequences of the same gene can differ through naturally occurring variations (e.g. polymorphisms), each with its own valid existence. This clone is substantially in agreement with the reference, but a complete review of all prevailing variants is recommended prior to use. More info
OTI Annotation This clone was engineered to express the complete ORF with an expression tag. Expression varies depending on the nature of the gene.
Shipping Dry Ice
Reference Data
RefSeq NM_005625.3
RefSeq Size 2173 bp
RefSeq ORF 897 bp
Locus ID 6386
UniProt ID O00560
Cytogenetics 8q12.1
Domains PDZ
Protein Families Druggable Genome, Transmembrane
MW 32.4 kDa
Summary The protein encoded by this gene was initially identified as a molecule linking syndecan-mediated signaling to the cytoskeleton. The syntenin protein contains tandemly repeated PDZ domains that bind the cytoplasmic, C-terminal domains of a variety of transmembrane proteins. This protein may also affect cytoskeletal-membrane organization, cell adhesion, protein trafficking, and the activation of transcription factors. The protein is primarily localized to membrane-associated adherens junctions and focal adhesions but is also found at the endoplasmic reticulum and nucleus. Alternative splicing results in multiple transcript variants encoding different isoforms. Related pseudogenes have been identified on multiple chromosomes. [provided by RefSeq, Jan 2017]
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