PGD recombinant monoclonal antibody
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Specification
Product Description
Rabbit recombinant monoclonal antibody raised against recombinant PGD.
Antibody Species
Rabbit
Immunogen
Original antibody is raised against a synthetic peptide of human PGD.
Theoretical MW (kDa)
52
Reactivity
Human, Mouse, Rat
Specificity
Recognizes endogenous levels of PGD protein.
Form
Liquid
Purification
Immunogen affinity chromatography
Isotype
IgG
Recommend Usage
Immunocytochemistry (1:50-1:100)
Immunofluorescence (1:50-1:100)
Immunoprecipitation(1:10-1:50)
Western Blot (1:500-1:1000)Storage Buffer
In 50mM Tris-Glycine, pH 7.4 (0.15M NaCl, 50% Glycerol, 0.01% Sodium azide and 0.05% BSA)
Storage Instruction
Store at 4°C short term.
Aliquot and store at -20°C long term.
Avoid freeze-thaw cycles.Note
This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Applications
Western Blot (Cell lysate)
Western blot analysis of C6 (A), NIH3T3 (B), Hela (C) whole cell lysates with PGD recombinant monoclonal antibody (Cat # RAB02418).Immunocytochemistry
Immunofluorescence
Immunofluorescent analysis of HeLa cells with PGD recombinant monoclonal antibody (Cat # RAB02418). Formalin-fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 5-10 minutes and blocked with 3% BSA-PBS for 30 minutes at room temperature. Cells were probed with the primary antibody in 3% BSA-PBS and incubated overnight at 4 °C in a hidified chamber. Cells were washed with PBST and incubated with a AF488-conjugated secondary antibody (green) in PBS at room temperature in the dark.Immunoprecipitation
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Gene Info — PGD
Entrez GeneID
5226Protein Accession#
P52209Gene Name
PGD
Gene Alias
6PGD
Gene Description
phosphogluconate dehydrogenase
Omim ID
172200Gene Ontology
HyperlinkGene Summary
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. [provided by RefSeq
Other Designations
6-phosphogluconate dehydrogenase
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