GPSM2 Antikörper

Produktnummer ABIN6566981

Produktdetails anti-GPSM2 Antikörper

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

Reaktivität: Human, Maus

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser GPSM2 Antikörper ist unkonjugiert

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

Aufreinigung: Affinity purification

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

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB 1:1000-1:2000 IHC 1:50-1:200

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1 mg/mL

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

Konservierungsmittel: Sodium azide

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

Lagerung: -20 °C

Informationen zur Lagerung: Store at -20°C. Avoid freeze / thaw cycles.

Details zu GPSM2

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

Andere Bezeichnung: GPSM2 (GPSM2 Produkte)

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

Hintergrund: 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.

Molekulargewicht:

Observed_MW: 77kDa

Calculated_MW: 76kDa

Gen-ID: 29899

UniProt: P81274

Pathways: Regulation of G-Protein Coupled Receptor Protein Signaling