G6PD Rabbit Monoclonal Antibody (CAB11234)
- SKU:
- CAB11234
- Product Type:
- Antibody
- Reactivity:
- Human
- Host Species:
- Rabbit
- Isotype:
- IgG
- Antibody Type:
- Monoclonal Antibody
- Research Area:
- Metabolism
Frequently bought together:
Description
Product Name: | G6PD Rabbit Monoclonal Antibody |
SKU: | CAB11234 |
Size: | 20uL, 100uL |
Isotype: | IgG |
Host Species: | Rabbit |
Reactivity: | Human |
Immunogen: | A synthetic peptide corresponding to a sequence within amino acids 400-500 of human G6PD (P11413). |
Sequence: | VYTK MMTK KPGM FFNP EESE LDLT YGNR YKNV KLPD AYER LILD VFCG SQMH FVRS DELR EAWR IFTP LLHQ IELE KPKP IPYI YGSR GPTE ADEL MKRV G |
Tested Applications: | WB ELISA |
Recommended Dilution: | WB,1:500 - 1:2000 |
Synonyms: | G6PD1; G6PD |
Positive Sample: | HeLa,MCF7 |
Conjugate: | Unconjugated |
Cellular Localization: | Cytoplasm, Cytoplasmic side of plasma membrane, cytosol, Extracellular exosome, Nucleus |
Calculated MW: | 59kDa |
Observed MW: | 59kDa |
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.
Purification Method: | Affinity purification |
Gene ID: | 2539 |
Clone Number: | ARC0553 |
Storage Buffer: | Store at -20℃. Avoid freeze / thaw cycles.Buffer: PBS with 0.02% sodium azide,0.05% BSA,50% glycerol,pH7.3. |