GPR172B Antikörper

Produktnummer ABIN7239008

Produktdetails anti-GPR172B Antikörper

Target: GPR172B (G Protein-Coupled Receptor 172B (GPR172B))

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser GPR172B Antikörper ist unkonjugiert

Applikation: ELISA, Immunohistochemistry (IHC)

Produktmerkmale: Polyclonal Antibody

Aufreinigung: Affinity purification

Immunogen: Synthetic peptide of human SLC52A1

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: IHC 1:50-1:200

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 0.8 mg/mL

Buffer: PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4

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 GPR172B

Target: GPR172B (G Protein-Coupled Receptor 172B (GPR172B))

Andere Bezeichnung: GPR172B (GPR172B Produkte)

Synonyme: GPR172A antikoerper, MGC79729 antikoerper, GPR172B antikoerper, gpcr41 antikoerper, GPCR42 antikoerper, PAR2 antikoerper, RBFVD antikoerper, RFT1 antikoerper, RFVT1 antikoerper, hRFT1 antikoerper, Gpr172a antikoerper, Gpr172b antikoerper, RGD1560410 antikoerper, rRFT1 antikoerper, POPAR antikoerper, 2010003P03Rik antikoerper, D15Ertd747e antikoerper, mRFT1 antikoerper, solute carrier family 52 member 1 antikoerper, solute carrier family 52 member 2 antikoerper, solute carrier family 52 (riboflavin transporter), member 1 antikoerper, solute carrier family 52 (riboflavin transporter), member 1 L homeolog antikoerper, solute carrier protein 52, member 2 antikoerper, SLC52A1 antikoerper, SLC52A2 antikoerper, slc52a1 antikoerper, slc52a1.L antikoerper, Slc52a2 antikoerper

Hintergrund: Biological redox reactions require electron donors and acceptor. Vitamin B2 is the source for the flavin in flavin adenine dinucleotide (FAD) and flavin mononucleotide (FMN) which are common redox reagents. This gene encodes a member of the riboflavin (vitamin B2) transporter family. Haploinsufficiency of this protein can cause maternal riboflavin deficiency. Multiple alternatively spliced variants, encoding the same protein, have been identified.

NCBI Accession: NP_001098047

UniProt: Q9NWF4