PYGM Monoclonal Antibody (OTI5D1), Invitrogen™
Manufacturer: Thermo Scientific
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | PIMA527442-Each-of-1 | In Stock | ₹ 52,198.50 |
PIMA527442 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 52,198.50
GST (18%): ₹ 9,395.73
Total Price: ₹ 61,594.23
Antigen
PYGM
Classification
Monoclonal
Concentration
1 mg/mL
Formulation
PBS with 1% BSA, 50% glycerol and 0.02% sodium azide; pH 7.3
Gene Accession No.
P09812, P11217, Q9WUB3
Gene Symbols
PYGM
Immunogen
Human recombinant protein fragment corresponding to amino acids 698-842 of PYGM produced in E.coli
Quantity
100μL
Primary or Secondary
Primary
Target Species
Human, Mouse, Rat
Product Type
Antibody
Isotype
IgG1
Applications
Immunohistochemistry (Paraffin), Western Blot
Clone
OTI5D1
Conjugate
Unconjugated
Gene
PYGM
Gene Alias
AI115133; glycogen muscle; glycogen phosphorylase; glycogen phosphorylase, muscle associated; glycogen phosphorylase, muscle form; GPMM; muscle (McArdle syndrome); muscle glycogen phosphorylase; Muscpho; Myophosphorylase; PG; Phosphorylase glycogen; phosphorylase, glycogen, muscle; Phosphorylase, glycogen; muscle (McArdle syndrome); Pygm; unnamed protein product
Host Species
Mouse
Purification Method
Affinity Chromatography
Regulatory Status
RUO
Gene ID (Entrez)
19309, 24701, 5837
Content And Storage
-20° C, Avoid Freeze/Thaw Cycles
Form
Liquid
Related Products
Description
- 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.