Glucose-6-Phosphate Dehydrogenase antibody
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- Target See all Glucose-6-Phosphate Dehydrogenase (G6PD) Antibodies
- Glucose-6-Phosphate Dehydrogenase (G6PD)
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Reactivity
- Human
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Host
- Mouse
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Clonality
- Monoclonal
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Conjugate
- This Glucose-6-Phosphate Dehydrogenase antibody is un-conjugated
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Application
- Western Blotting (WB), Immunohistochemistry (IHC), ELISA, Flow Cytometry (FACS)
- Purpose
- G6PD Antibody
- Purification
- Ascitic fluid
- Immunogen
- Purified recombinant fragment of human G6PD expressed in E. Coli.
- Clone
- 5E12
- Isotype
- IgG1
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- Application Notes
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ELISA: 1/10000
FCM: 1/200 - 1/400
- Restrictions
- For Research Use only
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- Format
- Liquid
- Buffer
- Ascitic fluid containing 0.03 % 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
- 4 °C,-20 °C
- Storage Comment
- Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.
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Positively selected G6PD-Mahidol mutation reduces Plasmodium vivax density in Southeast Asians." in: Science (New York, N.Y.), Vol. 326, Issue 5959, pp. 1546-9, (2009) (PubMed).
: "Effects of aging on antioxidant response and phagocytosis in senescent erythrocytes." in: Immunological investigations, Vol. 38, Issue 6, pp. 551-9, (2009) (PubMed).
: "
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Positively selected G6PD-Mahidol mutation reduces Plasmodium vivax density in Southeast Asians." in: Science (New York, N.Y.), Vol. 326, Issue 5959, pp. 1546-9, (2009) (PubMed).
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- Target
- Glucose-6-Phosphate Dehydrogenase (G6PD)
- Alternative Name
- G6PD (G6PD Products)
- Background
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Description: This gene encodes glucose-6-phosphate dehydrogenase. This protein is a cytosolic enzyme encoded by a housekeeping X-linked gene whose main function is to produce NADPH, a key electron donor in the defense against oxidizing agents and in reductive biosynthetic reactions. G6PD is remarkable for its genetic diversity. Many variants of G6PD, mostly produced from missense mutations, have been described with wide ranging levels of enzyme activity and associated clinical symptoms. G6PD deficiency may cause neonatal jaundice, acute hemolysis, or severe chronic non-spherocytic hemolytic anemia. Two transcript variants encoding different isoforms have been found for this gene.
Aliases: G6PD1
- Molecular Weight
- 59kDa
- Gene ID
- 2539
- HGNC
- 2539
- UniProt
- P11413
- Pathways
- Regulation of Systemic Arterial Blood Pressure by Hormones
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