Glucose-6-Phosphate Dehydrogenase antibody (Middle Region)
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- Target See all Glucose-6-Phosphate Dehydrogenase (G6PD) Antibodies
- Glucose-6-Phosphate Dehydrogenase (G6PD)
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Binding Specificity
- Middle Region
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Reactivity
- Human
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This Glucose-6-Phosphate Dehydrogenase antibody is un-conjugated
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Application
- Western Blotting (WB)
- Specificity
- G6 PD antibody was raised against the middle region of G6 D
- Purification
- Affinity purified
- Immunogen
- G6 PD antibody was raised using the middle region of G6 D corresponding to a region with amino acids VTKNIHESCMSQIGWNRIIVEKPFGRDLQSSDRLSNHISSLFREDQIYRI
- Top Product
- Discover our top product G6PD Primary Antibody
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- Application Notes
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WB: 1 µg/mL
Optimal conditions should be determined by the investigator. - Comment
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G6PD Blocking Peptide, catalog no. 33R-9850, is also available for use as a blocking control in assays to test for specificity of this G6PD antibody
- Restrictions
- For Research Use only
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- Format
- Lyophilized
- Reconstitution
- Lyophilized powder. Add distilled water for a 1 mg/mL concentration of G0 D antibody in PBS
- Concentration
- Lot specific
- Buffer
- PBS
- Handling Advice
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Avoid repeated freeze/thaw cycles.
Dilute only prior to immediate use. - Storage
- 4 °C/-20 °C
- Storage Comment
- Store at 2-8 °C for short periods. For longer periods of storage, store at -20 °C.
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- Target
- Glucose-6-Phosphate Dehydrogenase (G6PD)
- Alternative Name
- G6PD (G6PD Products)
- Background
- G6PD is a 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.
- Molecular Weight
- 57 kDa (MW of target protein)
- Pathways
- Regulation of Systemic Arterial Blood Pressure by Hormones
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