PYGM polyclonal antibody
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Specification
Product Description
Rabbit polyclonal antibody raised against synthetic peptide of PYGM.
Immunogen
A synthetic peptide (conjugated with KLH) corresponding to human PYGM.
Host
Rabbit
Reactivity
Human
Specificity
C-terminal domain of human .
Form
Liquid
Purification
Immunoaffinity purification
Recommend Usage
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) (20 ug/mL)
The optimal working dilution should be determined by the end user.Storage Buffer
In PBS (0.09% sodium azide)
Storage Instruction
Store at 4°C. For long term storage store at -80°C.
Aliquot to avoid repeated freezing and thawing.Note
This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Applications
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
Immunohistochemical (Formalin/PFA-fixed paraffin-embedded sections) staining of human skeletal muscle with PYGM polyclonal antibody (Cat # PAB16213). -
Gene Info — PYGM
Entrez GeneID
5837Protein Accession#
P11217Gene Name
PYGM
Gene Alias
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Gene Description
phosphorylase, glycogen, muscle
Gene Ontology
HyperlinkGene Summary
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
Other Designations
McArdle syndrome|glycogen phosphorylase|glycogen storage disease type V|myophosphorylase|phosphorylase, glycogen; muscle (McArdle syndrome, glycogen storage disease type V)
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Interactome
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Pathway
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Disease
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