ArtNr |
E-AB-15321-200 |
Hersteller |
Elabscience
|
Menge |
200uL |
Kategorie |
|
Typ |
Antibody Polyclonal |
Applikationen |
WB, IHC, ELISA |
Specific against |
Human, Mouse, Rat |
Host |
Rabbit |
Isotype |
IgG |
ECLASS 10.1 |
32160702 |
ECLASS 11.0 |
32160702 |
UNSPSC |
12352203 |
Alias |
Glycogen phosphorylase, Glycogen phosphorylase muscle form, muscle form, Muscpho, Myophosphorylase, Phosphorylase glycogen muscle (McArdle syndrome glycogen storage disease type V), Pygm, PYGM |
Similar products |
Pygm, Glycogen phosphorylase, PYGM, muscle form, Myophosphorylase, Glycogen phosphorylase muscle form, Muscpho, Phosphorylase glycogen muscle (McArdle syndrome glycogen storage disease type V) |
Lieferbar |
|
Research Areas |
Cancer, Metabolism, Signal Transduction |
Synonyms |
Glycogen phosphorylase, Glycogen phosphorylase muscle form, muscle form, Muscpho, Myophosphorylase, Phosphorylase glycogen muscle (McArdle syndrome glycogen storage disease type V), Pygm, PYGM |
Swissprot |
P11217 |
Background |
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. |
Concentration |
0.4 mg/mL |
Storage |
Store at -20C. Avoid freeze / thaw cycles. |
Immunogen |
Recombinant protein of human PYGM |
Buffer |
PBS with 0.05% sodium azide and 50% glycerol, PH7.4 |
Purification Method |
Affinity purification |
Dilution |
WB 1:500-1:2000, IHC 1:30-1:150 |
Conjugation |
Unconjugated |
Calculated MW |
97kDa |
Gene Accession |
BC126392 |
Santa Cruz # |
sc-130860 |
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