PFKM anticorps

N° du produit ABIN5703722

L’anticorps Lapin Polyclonal anti-PFKM a été validé pour WB, IHC, ELISA, IF et IP. Il convient pour détecter PFKM dans des échantillons de Humain, Souris et Rat.

Aperçu rapide pour PFKM anticorps (ABIN5703722)

Antigène: PFKM (phosphofructokinase, Muscle (PFKM))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp PFKM est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (IHC), ELISA, Immunofluorescence (IF), Immunoprecipitation (IP)

Détail du produit anti-PFKM anticorps

Fonction: PFKM antibody

Immunogène: phosphofructokinase, muscle

Isotype: IgG

Information d'application

Indications d'application: WB : 1:500-1:5000 IP : 1:500-1:5000 IHC : 1:20-1:200 IF : 1:10-1:100

Commentaires:

human skeletal muscle tissue were subjected to SDS PAGE followed by western blot with FNab06341(PFKM antibody) at dilution of 1:800

Restrictions: For Research Use only

Stockage

Buffer: PBS with 0.02 % sodium azide and 50 % glycerol pH 7.3,

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.

Conseil sur la manipulation: Avoid repeated freeze / thaw cycles.

Stock: -20 °C

Stockage commentaire: -20°C for 12 months

Date de péremption: 12 months

Détails sur PFKM

Antigène: PFKM (phosphofructokinase, Muscle (PFKM))

Autre désignation: PFKM

Sujet:

Synonyms: ATP-dependent 6-phosphofructokinase, muscle type (ATP-PFK, PFK-M)|6-phosphofructokinase type A|Phosphofructo-1-kinase isozyme A (PFK-A)|Phosphohexokinase|PFKM|PFKX

Background: Three phosphofructokinase isozymes exist in humans: muscle, liver and platelet. These isozymes function as subunits of the mammalian tetramer phosphofructokinase, which catalyzes the phosphorylation of fructose-6-phosphate to fructose-1, 6-bisphosphate. Tetramer composition varies depending on tissue type. This gene encodes the muscle-type isozyme. Mutations in this gene have been associated with glycogen storage disease type VII, also known as Tarui disease. Alternatively spliced transcript variants have been described.

Poids moléculaire: 75-85 kDa

ID gène: 5213

UniProt: P08237

Pathways: Positive Regulation of Peptide Hormone Secretion, Negative Regulation of Hormone Secretion, Carbohydrate Homeostasis, L'effet Warburg