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Glucose 6 Phosphate Dehydrogenase Antibody (2F6) - BSA Free

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Western Blot: Glucose 6 Phosphate Dehydrogenase Antibody (2F6) [NBP1-30358] - Lane 1. MCF cell lysate, Lane 2. HeLa cell lysate, Lane 3. Jurkat cell lysate.
Immunocytochemistry/ Immunofluorescence: Glucose 6 Phosphate Dehydrogenase Antibody (2F6) [NBP1-30358] - Analysis in HeLa cells line, stained with DAPI (Blue) for nucleus staining and monoclonal anti-human G6PD antibody ...read more

Product Details

Summary
Reactivity HuSpecies Glossary
Applications WB, ELISA, ICC/IF
Clone
2F6
Clonality
Monoclonal
Host
Mouse
Conjugate
Unconjugated
Format
BSA Free
Concentration
1.0 mg/ml

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Glucose 6 Phosphate Dehydrogenase Antibody (2F6) - BSA Free Summary

Immunogen
Recombinant human Glucose 6 Phosphate Dehydrogenase (35-506aa) purified from E. coli
Marker
Cytosol Marker
Isotype
IgG2b Kappa
Clonality
Monoclonal
Host
Mouse
Gene
G6PD
Purity
Protein G purified
Innovator's Reward
Test in a species/application not listed above to receive a full credit towards a future purchase.

Applications/Dilutions

Dilutions
  • ELISA 1:100-1:2000
  • Immunocytochemistry/ Immunofluorescence 1:100
  • Western Blot 1:1000-1:2000

Packaging, Storage & Formulations

Storage
Store at 4C short term. Aliquot and store at -20C long term. Avoid freeze-thaw cycles.
Buffer
PBS (pH 7.4), 10% Glycerol
Preservative
0.02% Sodium Azide
Concentration
1.0 mg/ml
Purity
Protein G purified

Alternate Names for Glucose 6 Phosphate Dehydrogenase Antibody (2F6) - BSA Free

  • G6PD
  • G6PD1EC 1.1.1.49
  • G6PDH
  • glucose-6-phosphate dehydrogenase

Background

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. [provided by RefSeq]. Transcript Variant: This variant (1) represents the longer transcript and encodes the longer isoform (a). This full-length 545 aa form has been reported to be inactive, but may be processed to the smaller (515 aa) active form. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.

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.

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Publications for Glucose 6 Phosphate Dehydrogenase Antibody (NBP1-30358) (0)

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Product General Protocols

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Video Protocols

WB Video Protocol
ICC/IF Video Protocol

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Secondary Antibodies

 

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Bioinformatics

Gene Symbol G6PD
Entrez
Uniprot