PGD Antibody (S02-7C6)

Western Blot: PGD Antibody (S02-7C6) [NBP3-19520] - Western blot detection of PGD in C6, 3T3, Hela cell lysates using NBP3-19520 (1:1000 diluted). Predicted band size: 53kDa. Observed band size: 49kDa.

Immunocytochemistry/Immunofluorescence: PGD Antibody (S02-7C6) [NBP3-19520] - Immunofluorescence of PGD (green) in Hela cells using NBP3-19520 at dilution 1/200, and DAPI (blue)

• Reactivity: Hu, Mu, Rt
• Applications: WB, ICC/IF
• Clone: S02-7C6
• Clonality: Monoclonal
• Host: Rabbit
• Conjugate: Unconjugated
• Concentration: 0.3 mg/ml

PGD Antibody (S02-7C6) Summary

• Description: Novus Biologicals Rabbit PGD Antibody (S02-7C6) (NBP3-19520) is a recombinant monoclonal antibody validated for use in WB and ICC/IF. All Novus Biologicals antibodies are covered by our 100% guarantee.
• Additional Information: Recombinant Monoclonal Antibody
• Immunogen: A synthetic peptide of human PGD (Uniprot # P52209)
• Source: HEK293
• Isotype: IgG
• Clonality: Monoclonal
• Host: Rabbit
• Gene: PGD
• Purity: Affinity purified

Applications/Dilutions

• Dilutions:
  • Immunocytochemistry/ Immunofluorescence 1/50-1/200
  • Western Blot 1/1000-1/5000
• Theoretical MW: 49 kDa.
  Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors.

Packaging, Storage & Formulations

• Storage: Store at 4C short term. Aliquot and store at -20C long term. Avoid freeze-thaw cycles.
• Buffer: 50mM Tris-Glycine(pH 7.4), 0.15M NaCl, 40% Glycerol, 0.05% BSA
• Preservative: 0.01% Sodium Azide
• Concentration: 0.3 mg/ml
• Purity: Affinity purified

Alternate Names for PGD Antibody (S02-7C6)

• 6PGD
• EC 1.1.1.44,6-phosphogluconate dehydrogenase, decarboxylating
• PGD
• PGDH
• phosphogluconate dehydrogenase

Background

6-phosphogluconate dehydrogenase 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.

Limitations

This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.

Bioinformatics

• Gene Symbol: PGD