GPSM2 anticorps

N° du produit ABIN7255365

Détail du produit anti-GPSM2 anticorps

Antigène: GPSM2 (G-Protein Signaling Modulator 2 (GPSM2))

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp GPSM2 est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (IHC)

Attributs du produit: Polyclonal Antibody

Purification: Affinity purification

Immunogène: Recombinant fusion protein of human GPSM2 (NP_037428.3).

Isotype: IgG

Information d'application

Indications d'application: WB 1:1000-1:2000 IHC 1:50-1:200

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

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 GPSM2

Antigène: GPSM2 (G-Protein Signaling Modulator 2 (GPSM2))

Autre désignation: GPSM2 (GPSM2 Produits)

Synonymes: anticorps CMCS, anticorps DFNB82, anticorps LGN, anticorps PINS, anticorps dfnb82, anticorps lgn, anticorps pins, anticorps RGD1560967, anticorps Pinsa, anticorps zgc:63574, anticorps 6230410J09Rik, anticorps Pins, anticorps G protein signaling modulator 2, anticorps G-protein signaling modulator 2 S homeolog, anticorps G-protein signaling modulator 2, anticorps G-protein signalling modulator 2 (AGS3-like, C. elegans), anticorps GPSM2, anticorps gpsm2.S, anticorps Gpsm2, anticorps gpsm2

Sujet: The protein encoded by this gene belongs to a family of proteins that modulate activation of G proteins, which transduce extracellular signals received by cell surface receptors into integrated cellular responses. The N-terminal half of this protein contains 10 copies of leu-gly-asn (LGN) repeat, and the C-terminal half contains 4 GoLoco motifs, which are involved in guanine nucleotide exchange. This protein may play a role in neuroblast division and in the development of normal hearing. Mutations in this gene are associated with autosomal recessive nonsyndromic deafness (DFNB82). Alternative splicing results in multiple transcript variants.

Poids moléculaire:

Observed_MW: 76 kDa

Calculated_MW: 76 kDa

ID gène: 29899

UniProt: P81274

Pathways: Regulation of G-Protein Coupled Receptor Protein Signaling