PGD antibody (AA 40-120)

Catalog No. ABIN7223134

The Rabbit Polyclonal anti-PGD antibody has been validated for WB and ELISA. It is suitable to detect PGD in samples from Human, Mouse and Rat.

Quick Overview for PGD antibody (AA 40-120) (ABIN7223134)

Target: PGD (Phosphogluconate Dehydrogenase (PGD))

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This PGD antibody is un-conjugated

Application: Western Blotting (WB), ELISA

Product Details anti-PGD Antibody

Binding Specificity: AA 40-120

Purpose: PGD Polyclonal Antibody

Specificity: PGD Polyclonal Antibody detects endogenous levels of PGD protein.

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

Immunogen: Synthesized peptide derived from the Internal region of human PGD at AA range: 40-120

Isotype: IgG

Application Details

Application Notes: Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB (1:500-1:2000), ELISA (1:5000). Not yet tested in other applications.

Comment:

Primary Antibody

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 mg/mL

Buffer: PBS containing 50 % Glycerol, 0.5 % BSA and 0.02 % Sodium Azide.

Preservative: Sodium azide

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

Storage: -20 °C

Storage Comment: 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.

Target Details for PGD

Target: PGD (Phosphogluconate Dehydrogenase (PGD))

Alternative Name: PGD

Background: Rabbit Anti-PGD Polyclonal Antibody,PGD, PGDH, 6-phosphogluconate dehydrogenase, decarboxylating,6-phosphogluconate dehydrogenase (PGD) is the second dehydrogenase in the pentose phosphate shunt. Deficiency of this enzyme is generally asymptomatic, and the inheritance of this disorder is autosomal dominant. Hemolysis results from combined deficiency of 6-phosphogluconate dehydrogenase and 6-phosphogluconolactonase suggesting a synergism of the two enzymopathies. Several transcript variants encoding different isoforms have been found for this gene.,6-phosphogluconate dehydrogenase decarboxylating

Molecular Weight: observerd band 40kDa

Gene ID: 5226

UniProt: P52209