PGAM1 Mouse Monoclonal Antibody [Clone ID: AT1G4]
CAT#: AM50618PU-N
PGAM1 mouse monoclonal antibody, clone AT1G4, Purified
Size: 50 ul
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CNY 6,620.00
货期*
5周
规格
Specifications
Product Data | |
Clone Name | AT1G4 |
Applications | ELISA, FC, IF, WB |
Recommend Dilution | The antibody has been tested by ELISA, Western blot analysis, ICC/IF and Flow cytometry to assure specificity and reactivity. Since application varies, however, each investigation should be titrated by the reagent to obtain optimal results. |
Reactivity | Human |
Host | Mouse |
Clonality | Monoclonal |
Immunogen | Recombinant human PGAM1 (1-254aa) purified from E. coli. |
Formulation | Liquid. In Phosphate-Buffered Saline (pH 7.4) with 0.02% Sodium Azide, 10% Glycerol. State: Purified State: Liquid purified Ig fraction |
Concentration | lot specific |
Purification | Protein-A affinity chromatography |
Conjugation | Unconjugated |
Storage Condition | Store undiluted at 2-8°C for one month or (in aliquots) at -20°C for longer. Avoid repeated freezing and thawing. |
Gene Name | phosphoglycerate mutase 1 |
Database Link | |
Background | PGAM1 belongs to the phosphoglycerate mutase family. This protein is important components of glucose and 2,3-BPGA (2,3-bisphosphoglycerate) metabolism and catalyzes the reversible reaction of 3-phosphoglycerate (3-PGA) to 2-phosphoglycerate (2-PGA) in the glycolytic pathway. The PGAM is a dimeric enzyme containing, in different tissues, different proportions of a slow-migrating muscle (MM) isozyme, a fast-migrating brain (BB) isozyme, and a hybrid form (MB). Mutations in this protein cause muscle phosphoglycerate mutase eficiency, also known as glycogen storage disease X. |
Synonyms | PGAM 1, Phosphoglycerate mutase 1, PGAMA, PGAM-B |
Reference Data | |
Protein Pathways | Glycolysis / Gluconeogenesis, Metabolic pathways |
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