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PYGM encodes a muscle enzyme involved in glycogenolysis. Additionally we are shipping Phosphorylase, Glycogen, Muscle Proteins (14) and Phosphorylase, Glycogen, Muscle Kits (10) and many more products for this protein.
Showing 10 out of 77 products:
Human Polyclonal PYGM Primary Antibody for EIA, WB - ABIN4620508
Tsoi, Cale, Bird, Kay: cDNA microarray analysis of gene expression profiles in human placenta: up-regulation of the transcript encoding muscle subunit of glycogen phosphorylase in preeclampsia. in Journal of the Society for Gynecologic Investigation 2003
Show all 4 references for ABIN4620508
Mouse (Murine) Polyclonal PYGM Primary Antibody for WB - ABIN610863
Adams, Dörfler, Aguzzi, Kozmik, Urbánek, Maurer-Fogy, Busslinger: Pax-5 encodes the transcription factor BSAP and is expressed in B lymphocytes, the developing CNS, and adult testis. in Genes & development 1992
Show all 3 references for ABIN610863
Human Polyclonal PYGM Primary Antibody for IF (p), IHC (p) - ABIN708356
de Luna, Brull, Lucia, Santalla, Garatachea, Martí, Andreu, Pinós: PYGM expression analysis in white blood cells: A complementary tool for diagnosing McArdle disease? in Neuromuscular disorders : NMD 2014
The horse PYGM gene was broadly expressed in all tissues tested with the highest expression observed in skeletal muscle. It contains fewer mobile elements than its human ortholog, resulting in an increase in the structural stability of the gene sequence.
Data suggest that the irreversible inhibition of glycogen (show GYS1 Antibodies) phosphorylase (GP) could represent one of the mechanisms that contribute to mercury-dependent muscle toxicity.
Data show that glycogen (show GYS1 Antibodies) phosphorylase is irreversibly impaired by exposure to peroxynitrite, and suggest that the peroxynitrite-dependent inactivation of the enzyme could be due to the nitration of Tyr613 at the allosteric inhibitor site of the enzyme.
The formation of a complex between the denatured monomeric form of Phb (show PHB Antibodies) and the dissociated forms of GroEL (show GroEL Antibodies) is detected during heating at 46 degrees C.
alpha-crystallin interacts with the intermediates of unfolding of the Phb (show PHB Antibodies) molecule
Variations in AMPD1 (show AMPD1 Antibodies), CPT2 (show CPT2 Antibodies), and PGYM genes are not associated with the onset, susceptibility, or severity of chronic fatigue syndrome.
update of the reported mutations and polymorphisms in the PYGM gene [review]
study found that T lymphocytes expressed myophosphorylase in healthy donors, but expression was significantly lower in McArdle patients (p<0.001); PYGM mRNA levels were also lower in white blood cells from McArdle patients
biological significance of this PKCtheta (show PRKCQ Antibodies);/alphaPIX (show ARHGEF6 Antibodies)/Rac 1 GTPase (show RACGAP1 Antibodies)/PYGM signaling pathway seems to be the control of different cellular responses such as migration and proliferation
5 different PYGM mutations were found in 8 Brazilian families: 4 previously described (p.R50X, p.T692kfs30, p.K609K, and p.G455R), and one, pI513V, a novel heterozygous mutation.
a novel mutation, in the PYGM gene c.632delG, in three unrelated families of Jewish descent originating from the Caucasus region
a new role for Rac1 in cell signaling, showing that this GTPase (show RACGAP1 Antibodies) triggers T-cell proliferation upon IL-2 (show IL2 Antibodies) stimulation by associating with PYGM and modulating its enzymatic activity.
No genotype-phenotype correlation is evident and that no gender effect is related to the phenotype of McArdle's disease (PYGM gene) in a cohort of 123 European McArdle's disease patients.
The current data add to the list of pathogenic mutations in the PYGM gene associated with McArdle disease
This study demonistrated that PYGM mutation in McArdle disease.
Data indicate that a G/T mutation in exon 8 in muscle glycogen phosphorylase (PYGM) was identified and association analysis with meat quality traits showed that it was significantly associated with lean meat percentage(p<0.05).
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.
, glycogen phosphorylase, muscle form
, phosphorylase, glycogen; muscle (McArdle syndrome, glycogen storage disease type V)
, phosphorylase, glycogen. muscle
, Phosphorylase glycogen
, Phosphorylase, glycogen; muscle (McArdle syndrome)
, muscle (McArdle syndrome)
, muscle glycogen phosphorylase
, glycogen myophosphorylase