Glucose 6 phosphate isomerase (GPI) Mouse Monoclonal Antibody [Clone ID: 1B7D7]
CAT#: AM06224SU-N
Glucose 6 phosphate isomerase (GPI) mouse monoclonal antibody, clone 1B7D7, Ascites
Other products for "GPI"
Specifications
Product Data | |
Clone Name | 1B7D7 |
Applications | ELISA, IF, IHC, WB |
Recommended Dilution | ELISA: 1/10000. Western Blot: 1/500 - 1/2000. Immunofluorescence: 1/200 - 1/1000. Immunohistochemistry on Paraffin Sections: 1/200 - 1/1000. |
Reactivities | Human |
Host | Mouse |
Isotype | IgG1 |
Clonality | Monoclonal |
Immunogen | Purified recombinant fragment of human GPI expressed in E. Coli. |
Specificity | Recognizes Glucose-6-phosphate isomerase |
Formulation | State: Ascites State: Ascitic fluid containing 0.03% Sodium Azide. |
Conjugation | Unconjugated |
Storage | Store the antibody undiluted at 2-8°C for one month or (in aliquots) at -20°C for longer. Avoid repeated freezing and thawing. |
Stability | Shelf life: one year from despatch. |
Gene Name | glucose-6-phosphate isomerase |
Database Link | |
Background | Glucose-6-phosphate isomerase, or phosphoglucose isomerase, also known as GPI. It belongs to the GPI family whose members encode multifunctional phosphoglucose isomerase proteins involved in energy pathways and it is an enzyme that catalyzes the conversion of glucose-6-phosphate into fructose 6-phosphate in the second step of glycolysis. The protein functions in different capacities inside and outside the cell. In the cytoplasm, the gene product is involved in glycolysis and gluconeogenesis, while outside the cell it functions as a neurotrophic factor for spinal and sensory neurons. Defects in GPI are the cause of nonspherocytic hemolytic anemia and a severe enzyme deficiency can be associated with hydrops fetalis, immediate neonatal death and neurological impairment. |
Synonyms | Phosphoglucose isomerase, PGI, Phosphohexose isomerase, PHI, Neuroleukin, NLK |
Reference Data |
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