GRHPR antibody (AA 51-150) (AbBy Fluor® 647)

Catalog No. ABIN6979977

This anti-GRHPR antibody is a Rabbit Polyclonal antibody detecting GRHPR in WB, IF (cc) and IF (p). Suitable for Mouse.

Quick Overview for GRHPR antibody (AA 51-150) (AbBy Fluor® 647) (ABIN6979977)

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

Reactivity: Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This GRHPR antibody is conjugated to AbBy Fluor® 647

Application: Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Product Details anti-GRHPR Antibody (AbBy Fluor® 647)

Binding Specificity: AA 51-150

Cross-Reactivity: Mouse

Predicted Reactivity: Human,Rat,Dog,Cow,Sheep,Horse,Chicken,Rabbit

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human GRHPR

Isotype: IgG

Application Details

Application Notes: IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

Preservative: ProClin

Precaution of Use: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

Storage: -20 °C

Storage Comment: Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Expiry Date: 12 months

Target Details for GRHPR

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

Alternative Name: GRHPR

Background:

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]

Gene ID: 9380

UniProt: Q9UBQ7