Vav3 (NM_020505) Mouse Tagged ORF Clone Lentiviral Particle

CAT#: MR210938L4V

  • LentiORF®

Lenti ORF particles, Vav3 (GFP-tagged) - Mouse vav 3 oncogene (Vav3), transcript variant 1, 200ul, >10^7 TU/mL

Lentiviral Particles: DDK w/ Puro mGFP w/ Puro



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USD 1,326.00

12 Weeks*

Size
    • 200 ul

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Specifications

Product Data
Type Mouse Tagged ORF Clone
Tag mGFP
Symbol Vav3
Synonyms A530094I06Rik; AA986410; Idd18.1
Mammalian Cell Selection Puromycin
Vector pLenti-C-mGFP-P2A-Puro
ACCN NM_020505
ORF Size 2541 bp
Sequence Data
The ORF insert of this clone is exactly the same as(MR210938).
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_020505.2, NP_065251.2
RefSeq Size 5023 bp
RefSeq ORF 2544 bp
Locus ID 57257
UniProt ID Q9R0C8
Cytogenetics 3 F3
Gene Summary Exchange factor for GTP-binding proteins RhoA, RhoG and, to a lesser extent, Rac1. Binds physically to the nucleotide-free states of those GTPases (By similarity). Plays an important role in angiogenesis. Its recruitment by phosphorylated EPHA2 is critical for EFNA1-induced RAC1 GTPase activation and vascular endothelial cell migration and assembly. May be important for integrin-mediated signaling, at least in some cell types. In osteoclasts, along with SYK tyrosine kinase, required for signaling through integrin alpha-v/beta-1 (ITAGV-ITGB1), a crucial event for osteoclast proper cytoskeleton organization and function. This signaling pathway involves RAC1, but not RHO, activation. Necessary for proper wound healing. In the course of wound healing, required for the phagocytotic cup formation preceding macrophage phagocytosis of apoptotic neutrophils. Responsible for integrin beta-2-mediated macrophage adhesion and, to a lesser extent, contributes to beta-3-mediated adhesion. Does not affect integrin beta-1-mediated adhesion.[UniProtKB/Swiss-Prot Function]

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