Mannose Phosphate Isomerase (MPI) Antibody
Por favor contáctenos para obtener información detallada sobre el precio y disponibilidad.
Description
MPI Antibody is a Rabbit Polyclonal Antibody against MPI.
Documents del producto
Product specifications
| Category | Primary Antibodies |
| Immunogen Target | Mannose Phosphate Isomerase (MPI) |
| Host | Rabbit |
| Reactivity | Human, Mouse, Rat |
| Recommended Dilution | ELISA: 1 µg/ml, WB: 1/500 - 1/2000. Optimal dilutions/concentrations should be determined by the end user. |
| Clonality | Polyclonal |
| Conjugation | Unconjugated |
| Isotype | IgG |
| Purification | Purified by affinity chromatography. |
| Size 1 | 20 µl |
| Size 2 | 100 µl |
| Size 3 | 2 × 100 µl |
| Form | Liquid |
| Tested Applications | ELISA, WB |
| Buffer | PBS, pH 7.3, containing 0.02% sodium azide, 50% glycerol. |
| Availability | Shipped within 5-10 working days. |
| Storage | Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles. |
| Dry Ice | No |
| UniProt ID | P34949 |
| Gene ID | 4351 |
| NCBI Accession | NP_002426.1 |
| Background | Antibody anti-MPI |
| Status | RUO |
| Note | Concentration: > 0.2 mg/ml - |
Descripción
Related Products
MPI antibody
Phosphomannose isomerase catalyzes the interconversion of fructose-6-phosphate and mannose-6-phosphate and plays a critical role in maintaining the supply of D-mannose derivatives, which are required for most glycosylation reactions. Mutations in the MPI gene were found in patients with carbohydrate-deficient glycoprotein syndrome, type Ib. Alternative splicing results in multiple transcript variants.
Ver Producto
Mannose Phosphate Isomerase (MPI) Antibody
MPI Antibody is a Rabbit Polyclonal Antibody against MPI.
Ver Producto
Mannose Phosphate Isomerase (MPI) Antibody
Phosphomannose isomerase catalyzes the interconversion of fructose-6-phosphate and mannose-6-phosphate and plays a critical role in maintaining the supply of D-mannose derivatives, which are required for most glycosylation reactions. Mutations in the MPI gene were found in patients with carbohydrate-deficient glycoprotein syndrome, type Ib.
Ver Producto