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Cow (Bovine) Polyclonal PYGM Primary Antibody für 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 Pubmed References
Human Polyclonal PYGM Primary Antibody für IF (p) - ABIN912619
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.
Results show that PYGM and RAC1 are altered in the dorsolateral prefrontal cortex in chronic schizophrenia and are controlled by NMDA signaling in the rodent cortex and cortical astrocytes suggesting an altered NMDA-dependent glycogenolysis in astrocytes in schizophrenia.
Data suggest that the irreversible inhibition of glycogen (zeige GYS1 Antikörper) phosphorylase (GP) could represent one of the mechanisms that contribute to mercury-dependent muscle toxicity.
Data show that glycogen (zeige GYS1 Antikörper) 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 (zeige PHB Antikörper) and the dissociated forms of GroEL (zeige GroEL Antikörper) is detected during heating at 46 degrees C.
alpha-crystallin interacts with the intermediates of unfolding of the Phb (zeige PHB Antikörper) molecule
This report expands the phenotype and genotype of McArdle disease and suggests that PYGM mutations should be looked for in patients with very late-onset myopathy with no previous history of exercise intolerance
Because the NMD mechanism does not seem to operate in nonspecific cells, PBMCs were more suitable than muscle biopsies for detecting the pathogenicity of some PYGM mutations, notably the silent mutation whose effect in the splicing of intron 6 was unnoticed in previous muscle transcriptomic studies
Variations in AMPD1 (zeige AMPD1 Antikörper), CPT2 (zeige CPT2 Antikörper), 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 (zeige PRKCQ Antikörper);/alphaPIX (zeige ARHGEF6 Antikörper)/Rac 1 GTPase (zeige RACGAP1 Antikörper)/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 (zeige RACGAP1 Antikörper) triggers T-cell proliferation upon IL-2 (zeige IL2 Antikörper) stimulation by associating with PYGM and modulating its enzymatic activity.
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