FAM65B anticorps

N° du produit ABIN6571960

Détail du produit anti-FAM65B anticorps

Antigène: FAM65B (Family with Sequence Similarity 65, Member B (FAM65B))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp FAM65B est non-conjugé

Application: Western Blotting (WB)

Purification: Affinity purification

Immunogène: Recombinant Protein of human FAM65B

Isotype: IgG

Information d'application

Indications d'application: WB 1:500 - 1:2000

Restrictions: For Research Use only

Stockage

Concentration: 1 mg/mL

Buffer: Buffer: PBS with 0.02 % sodium azide, 50 % glycerol,  pH 7.3.

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: Store at -20°C. Avoid freeze / thaw cycles.

Détails sur FAM65B

Antigène: FAM65B (Family with Sequence Similarity 65, Member B (FAM65B))

Autre désignation: FAM65B (FAM65B Produits)

Synonymes: anticorps C6orf32, anticorps DIFF40, anticorps DIFF48, anticorps MYONAP, anticorps PL48, anticorps 1700108N18Rik, anticorps 6330500D04Rik, anticorps AI225904, anticorps E430013J17Rik, anticorps si:dkey-218n20.1, anticorps Ab2-162, anticorps RGD1306939, anticorps RHO family interacting cell polarization regulator 2, anticorps family with sequence similarity 65, member B, anticorps ripor2, anticorps RIPOR2, anticorps Ripor2, anticorps FAM65B

Sujet:

Synonyms: RHO Family Interacting Cell Polarization Regulator 2,Family With Sequence Similarity 65 Member B,C6orf32,FAM65B,DIFF48,PL48,Myogenesis-Related And NCAM-Associated Protein Homolog,Rho Family-Interacting Cell Polarization Regulator 2,Family With Sequence Similarity 65, Member B,Chromosome 6 Open Reading Frame 32,Protein FAM65B,KIAA0386,DFNB104,DIFF40,MYONAP

Background: This gene encodes an atypical inhibitor of the small G protein RhoA. Inhibition of RhoA activity by the encoded protein mediates myoblast fusion and polarization of T cells and neutrophils. The encoded protein is a component of hair cell stereocilia that is essential for hearing. A splice site mutation in this gene results in hearing loss in human patients.

Poids moléculaire:

Observed_MW: 118kDa

Calculated_MW: 65kDa/118kDa

ID gène: 9750

UniProt: Q9Y4F9

Pathways: Transition Metal Ion Homeostasis