MPI anticorps (AA 25-75)

N° du produit ABIN7451179

Détail du produit anti-MPI anticorps

Antigène: MPI (Mannose Phosphate Isomerase (MPI))

Épitope: AA 25-75

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp MPI est non-conjugé

Application: Immunoprecipitation (IP)

Fonction: Rabbit anti-MPI Antibody, Affinity Purified

Homologie: Chimpanzee

Purification: Affinity Purified

Immunogène: Between AA 25 and 75

Isotype: IgG

Information d'application

Indications d'application:

IP: 2 - 10 μg/mg lysate

WB: Not recommended. ABIN7451179 has not performed satisfactorily when used for WB of MPI in crude preparations (e.g. whole cell lysate). This antibody can be used for WB of enriched (e.g. immunoprecipitated) sources of MPI.

Restrictions: For Research Use only

Stockage

Concentration: 1000 μg/mL

Buffer: Tris-citrate/phosphate buffer, pH 7 to 8 containing 0.09 % Sodium Azide

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: 4 °C

Date de péremption: 12 months

Détails sur MPI

Antigène: MPI (Mannose Phosphate Isomerase (MPI))

Autre désignation: MPI (MPI Produits)

Synonymes: anticorps CDG1B, anticorps PMI, anticorps PMI1, anticorps 1110002E17Rik, anticorps AI315153, anticorps Mpi-1, anticorps Mpi1, anticorps im:7140016, anticorps zgc:110773, anticorps cdg1b, anticorps pmi, anticorps pmi1, anticorps CaO19.1390, anticorps mannose phosphate isomerase, anticorps mannose phosphate isomerase S homeolog, anticorps mannose phosphate isomerase (mapped), anticorps mannose-6-phosphate isomerase, anticorps MPI, anticorps Mpi, anticorps mpi, anticorps mpi.S, anticorps PMI1

Sujet: Background: 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 [taken from NCBI Entrez Gene (Gene ID: 4351)].

ID gène: 4351

UniProt: P34949