Vav 3 Oncogene Phospho-Tyr173 (VAV3 pY173) Antibody

Este producto es parte de VAV - VAV guanine nucleotide exchange factor
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221€ (50 µg)

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935106861
info@markelab.com
name
Vav 3 Oncogene Phospho-Tyr173 (VAV3 pY173) Antibody
category
Primary Antibodies
provider
Abbexa
reference
abx325918
tested applications
ELISA, WB, IHC

Description

VAV3 (pY173) Antibody is a Rabbit Polyclonal against VAV3 (pY173).

Documents del producto

Instrucciones
Data sheet
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Product specifications

CategoryPrimary Antibodies
Immunogen TargetVav 3 Oncogene Phospho-Tyr173 (VAV3 pY173)
HostRabbit
ReactivityHuman, Mouse
Assay DataModification: Phosphorylation // Target Modification: Tyr173
Recommended DilutionELISA: 1/40000, WB: 1/500 - 1/2000, IHC: 1/100 - 1/300. Optimal dilutions/concentrations should be determined by the end user.
ClonalityPolyclonal
ConjugationUnconjugated
IsotypeIgG
PurificationPurified by affinity chromatography.
Size 150 µg
Size 2100 µg
FormLiquid
Tested ApplicationsELISA, WB, IHC
BufferPBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
AvailabilityShipped within 5-10 working days.
StorageAliquot and store at -20°C. Avoid repeated freeze/thaw cycles.
Dry IceNo
UniProt IDQ9UKW4
Gene ID10451
AliasVAV-3
BackgroundAntibody anti-VAV3
StatusRUO

Descripción

VAV3 is a member of the VAV family of guanine nucleotide exchange factors (GEFs) that regulate Rho family GTPases, such as Rac1, RhoA, and Cdc42, to mediate cytoskeletal reorganization, cell migration, and proliferation. VAV3 is expressed in multiple tissues, including the brain, endothelial cells, and immune cells, where it functions in signaling pathways downstream of receptor tyrosine kinases (RTKs), integrins, and immune receptors. It is involved in processes like angiogenesis, neuronal development, and immune cell activation. Dysregulation of VAV3 is associated with cancer, where it promotes tumor cell migration, metastasis, and survival through Rac1 activation and integrin signaling. VAV3 also plays a role in immune responses, including T-cell activation and macrophage function. Knockout studies demonstrate impaired angiogenesis, defective immune cell migration, and reduced tumor metastasis, highlighting its essential role in cytoskeletal regulation, cell signaling, and tumor progression.

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