PYGM anticorps (AA 390-804)

N° du produit ABIN7825691

Cet anticorps anti-PYGM est un anticorps Lapin Polyclonal détectant PYGM dans WB, IHC, ELISA et FACS. Adapté pour Humain, Souris et Rat.

Aperçu rapide pour PYGM anticorps (AA 390-804) (ABIN7825691)

Antigène: PYGM (Phosphorylase, Glycogen, Muscle (PYGM))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp PYGM est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (IHC), ELISA, Flow Cytometry (FACS)

Détail du produit anti-PYGM anticorps

Épitope: AA 390-804

Fonction: Anti-PYGM Antibody

Réactivité croisée (Details): No cross-reactivity with other proteins

Attributs du produit: Anti-PYGM Antibody catalog # A02971-1. Tested in WB, IHC, Flow Cytometry, ELISA applications. This antibody reacts with Human, Mouse, Rat. This is a premium antibody that guarantees superior quality, high affinity, and strong signals with minimal background in Western blot applications.

Purification: Immunogen affinity purified.

Immunogène: E.coli-derived human PYGM recombinant protein (Position: V390-R804). Human PYGMshares 95.9% and 94.2% amino acid (aa) sequence identity with mouse and rat PYGM, respectively.

Isotype: IgG

Information d'application

Indications d'application: Western blot, 0.25-0.5 μg/mL, Mouse, Rat
Immunohistochemistry, 2-5 μg/mL, Human
Flow Cytometry (Fixed), 1-3 μg/1x10⁶ cells, Human
ELISA, 0.1-0.5 μg/mL

Restrictions: For Research Use only

Stockage

Format: Lyophilized

Reconstitution: Adding 0.2 mL of distilled water will yield a concentration of 500 μg/mL.

Concentration: 500 μg/mL

Buffer: Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.

Stock: 4 °C,-20 °C

Stockage commentaire: At -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freezing and thawing.

Détails sur PYGM

Antigène: PYGM (Phosphorylase, Glycogen, Muscle (PYGM))

Autre désignation: PYGM

Sujet: This gene encodes a muscle enzyme involved in glycogenolysis. Highly similar enzymes encoded by different genes are found in liver and brain. Mutations in this gene are associated with McArdle disease (myophosphorylase deficiency), a glycogen storage disease of muscle. Alternative splicing results in multiple transcript variants.

Poids moléculaire: 97 kDa

ID gène: 5837

UniProt: P11217

Pathways: Cellular Glucan Metabolic Process