SSH3BP1 (ABI1) (NM_005470) Human Tagged ORF Clone Lentiviral Particle
CAT#: RC217707L2V
- LentiORF®
Lenti ORF particles, ABI1 (mGFP-tagged) - Human abl-interactor 1 (ABI1), transcript variant 1, 200ul, >10^7 TU/mL
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CNY 10,735.00
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Specifications
Product Data | |
Product Name | SSH3BP1 (ABI1) (NM_005470) Human Tagged ORF Clone Lentiviral Particle |
Synonyms | ABI-1; ABLBP4; E3B1; NAP1BP; SSH3BP; SSH3BP1 |
Vector | pLenti-C-mGFP |
ACCN | NM_005470 |
ORF Size | 1353 bp |
Sequence Data |
The ORF insert of this clone is exactly the same as(RC217707).
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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. |
Reference Data | |
RefSeq | NM_005470.2 |
RefSeq Size | 3725 bp |
RefSeq ORF | 1527 bp |
Locus ID | 10006 |
Domains | SH3 |
MW | 55.1 kDa |
Gene Summary | This gene encodes a member of the Abelson-interactor family of adaptor proteins. These proteins facilitate signal transduction as components of several multiprotein complexes, and regulate actin polymerization and cytoskeletal remodeling through interactions with Abelson tyrosine kinases. The encoded protein plays a role in macropinocytosis as a component of the WAVE2 complex, and also forms a complex with EPS8 and SOS1 that mediates signal transduction from Ras to Rac. This gene may play a role in the progression of several malignancies including melanoma, colon cancer and breast cancer, and a t(10;11) chromosomal translocation involving this gene and the MLL gene has been associated with acute myeloid leukemia. 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 14. [provided by RefSeq, Sep 2011] |
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