Vav 3 Oncogene (VAV3) Antibody

Este producto es parte de VAV - VAV guanine nucleotide exchange factor
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416€ (200 µl)

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935106861
info@markelab.com
name
Vav 3 Oncogene (VAV3) Antibody
category
Primary Antibodies
provider
Abbexa
reference
abx433439
tested applications
P-ELISA, IHC, FCM

Description

VAV3 Antibody is a Goat Polyclonal antibody against VAV3.

Documents del producto

Instrucciones
Data sheet
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Product specifications

CategoryPrimary Antibodies
Immunogen TargetVav 3 Oncogene (VAV3)
HostGoat
ReactivityHuman
Recommended DilutionP-ELISA: 1/32000. Optimal dilutions/concentrations should be determined by the end user.
ClonalityPolyclonal
ConjugationUnconjugated
IsotypeIgG
PurificationPurified from goat serum by ammonium sulphate precipitation followed by antigen affinity chromatography using the immunizing peptide.
Size 1200 µl
FormLiquid
Tested ApplicationsP-ELISA, IHC, FCM
BufferTris saline, pH 7.3, containing 0.02% sodium azide and 0.5% bovine serum albumin.
AvailabilityShipped within 5-10 working days.
StorageAliquot and store at -20°C. Avoid repeated freeze/thaw cycles.
Dry IceNo
Gene ID10451
NCBI AccessionNP_006104.4, NP_001073343.1
AliasVAV-3
BackgroundAntibody anti-VAV3
StatusRUO
NoteConcentration: 0.5 mg/ml -

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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