GRHPR anticorps (AA 51-150) (Biotin)

N° du produit ABIN6943573

L’anticorps anti-GRHPR Polyclonal Lapin est utilisé pour la détection de GRHPR dans des échantillons de Humain. Il a été validé pour WB, IHC (p) et IHC (fro).

Aperçu rapide pour GRHPR anticorps (AA 51-150) (Biotin) (ABIN6943573)

Antigène: GRHPR (Glyoxylate Reductase/hydroxypyruvate Reductase (GRHPR))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp GRHPR est conjugé à/à la Biotin

Application: Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))

Détail du produit anti-GRHPR anticorps (Biotin)

Épitope: AA 51-150

Fonction: GRHPR Polyclonal Antibody, Biotin Conjugated

Réactivité croisée: Souris

Homologie: Human,Rat,Dog,Cow,Sheep,Horse,Chicken,Rabbit

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human GRHPR

Isotype: IgG

Information d'application

Indications d'application: WB(1:300-5000),

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.

Agent conservateur: ProClin

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

Stock: -20 °C

Stockage commentaire: Store at -20°C for 12 months.

Date de péremption: 12 months

Détails sur GRHPR

Antigène: GRHPR (Glyoxylate Reductase/hydroxypyruvate Reductase (GRHPR))

Autre désignation: GRHPR

Sujet:

Synonyms: GLXR, glycerate 2 dehydrogenase, GLYD, Glyoxylate reductase/hydroxypyruvate reductase, Grhpr, GRHPR_HUMAN, OTTHUMP00000021379, OTTHUMP00000021380, OTTHUMP00000046131, PH 2, PH2, Primary hyperoxaluria type 2.

Background: This gene encodes an enzyme with hydroxypyruvate reductase, glyoxylate reductase, and D-glycerate dehydrogenase enzymatic activities. The enzyme has widespread tissue expression and has a role in metabolism. Type II hyperoxaluria is caused by mutations in this gene. [provided by RefSeq, Jul 2008]

ID gène: 9380

UniProt: Q9UBQ7