ARG64218

anti-G6PD antibody

anti-G6PD antibody for Western blot and Human

Cancer antibody; Cell Biology and Cellular Response antibody; Metabolism antibody; Signaling Transduction antibody

Overview

Product Description Goat Polyclonal antibody recognizes G6PD
Tested Reactivity Hu
Predict Reactivity Ms, Rat, Dog
Tested Application WB
Specificity This antibody is expected to recognise both reported isoforms (NP_000393.4 and NP_001035810.1).
Host Goat
Clonality Polyclonal
Isotype IgG
Target Name G6PD
Antigen Species Human
Immunogen C-KPASTNSDDVRDEK
Conjugation Un-conjugated
Alternate Names G6PD1; G6PD; EC 1.1.1.49; Glucose-6-phosphate 1-dehydrogenase

Application Instructions

Application Suggestion
Tested Application Dilution
WB1 - 3 µg/ml
Application Note WB: Recommend incubate at RT for 1h.
* The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist.

Properties

Form Liquid
Purification Purified from goat serum by ammonium sulphate precipitation followed by antigen affinity chromatography using the immunizing peptide.
Buffer Tris saline (pH 7.3), 0.02% Sodium azide and 0.5% BSA
Preservative 0.02% Sodium azide
Stabilizer 0.5% BSA
Concentration 0.5 mg/ml
Storage Instruction For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C or below. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use.
Note For laboratory research only, not for drug, diagnostic or other use.

Bioinformation

Database Links

GeneID: 2539 Human G6PD

Swiss-port # P11413 Human Glucose-6-phosphate 1-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, Jul 2008]
Research Area Cancer antibody; Cell Biology and Cellular Response antibody; Metabolism antibody; Signaling Transduction antibody
Calculated MW 59 kDa
PTM Acetylated by ELP3 at Lys-403; acetylation inhibits its homodimerization and enzyme activity. Deacetylated by SIRT2 at Lys-403; deacetylation stimulates its enzyme activity.

Images (1) Click the Picture to Zoom In

  • ARG64218 anti-G6PD antibody WB image

    Western Blot: Peripheral Blood Mononucleocytes lysate (35 µg protein in RIPA buffer) stained with ARG64218 anti-G6PD (aa 305 - 318) antibody at 1 µg/ml dilution.