PYGM anticorps (C-Term)

N° du produit ABIN5531905

Détail du produit anti-PYGM anticorps

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

Épitope: AA 698-727, C-Term

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp PYGM est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Purification: This antibody is prepared by Saturated Ammonium Sulfate (SAS) precipitation followed by dialysis

Immunogène: This PYGM antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 698-727 amino acids from the C-terminal region of human PYGM.

Isotype: Ig Fraction

Information d'application

Indications d'application: For WB starting dilution is: 1:1000

For IHC-P starting dilution is: 1:10~50

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 2 mg/mL

Buffer: Supplied in PBS with 0.09 % (W/V) 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,-20 °C

Stockage commentaire: Store at 4°C for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.

Détails sur PYGM

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

Autre désignation: PYGM (PYGM Produits)

Synonymes: anticorps pygb, anticorps im:7150327, anticorps zgc:110706, anticorps AI115133, anticorps PG, anticorps Muscpho, anticorps zgc:63642, anticorps phosphorylase, glycogen, muscle L homeolog, anticorps glycogen phosphorylase, muscle associated, anticorps phosphorylase, glycogen, muscle A, anticorps glycogen phosphorylase, muscle form, anticorps muscle glycogen phosphorylase, anticorps phosphorylase, glycogen, muscle b, anticorps pygm.L, anticorps PYGM, anticorps pygma, anticorps THA_70, anticorps Pygm, anticorps pygmb

Sujet: PYGM catalyzes and regulates the breakdown of glycogen to glucose-1-phosphate. Defects in PYGM are the cause of glycogen storage disease type 5 (GSD5), also known as McArdle disease. GSD5 is a metabolic disorder resulting in myopathy characterized by exercise intolerance, cramps, muscle weakness and recurrent myoglobinuria.

Poids moléculaire: 97 kDa

ID gène: 5837

UniProt: P11217

Pathways: Cellular Glucan Metabolic Process