GPR143 anticorps (AA 120-200)

N° du produit ABIN7222854

Cet anticorps anti-GPR143 Polyclonal Lapin (ABIN7222854) détecte spécifiquement GPR143 dans ELISA et IF. L’anticorps est réactif avec des échantillons de Humain et Souris.

Aperçu rapide pour GPR143 anticorps (AA 120-200) (ABIN7222854)

Antigène: GPR143 (G Protein-Coupled Receptor 143 (GPR143))

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp GPR143 est non-conjugé

Application: ELISA, Immunofluorescence (IF)

Détail du produit anti-GPR143 anticorps

Épitope: AA 120-200

Fonction: Rabbit Anti-GPR143 Polyclonal Antibody

Specificité: GPR143 Polyclonal Antibody detects endogenous levels of GPR143 protein.

Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Immunogène: Synthesized peptide derived from the Internal region of human GPR143 at AA range: 120-200

Isotype: IgG

Information d'application

Indications d'application: Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: IF 1:200-1:1000,ELISA 1:10000,Not yet tested in other applications,

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: Liquid in PBS containing 50 % glycerol, 0.5 % BSA and 0.02 % sodium azide.

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: Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.

Date de péremption: 12 months

Détails sur GPR143

Antigène: GPR143 (G Protein-Coupled Receptor 143 (GPR143))

Autre désignation: GPR143

Sujet: GPR143, OA1, G-protein coupled receptor 143, Ocular albinism type 1 proteinGPR143 encodes a protein that binds to heterotrimeric G proteins and is targeted to melanosomes in pigment cells. This protein is thought to be involved in intracellular signal transduction mechanisms. Mutations in GPR143 cause ocular albinism type 1, also referred to as Nettleship-Falls type ocular albinism, a severe visual disorder. A related pseudogene has been identified on chromosome Y.

ID gène: 4935

UniProt: P51810