General description
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.
Immunogen
PYGM (NP_005600, 522-556)
This antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide selected from the center region of human PYGM.
Physical form
Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide.
- UPC:
- 51201516
- Condition:
- New
- Availability:
- 3-5 Days
- Weight:
- 1.00 Ounces
- HazmatClass:
- No
- WeightUOM:
- LB
- MPN:
- SAB1300548-100UG
- Product Size:
- 100/µG