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Recombinant Human PYGM Protein, N-His

Catalog #:   YHC86801 Specific References (50) DATASHEET
Applications: ELISA, Immunogen, SDS-PAGE, WB, Bioactivity testing in progress
Expression system: E. coli
Accession: P11217
Protein length: Gly486-Gly827
Overview

Catalog No.

YHC86801

Expression system

E. coli

Species

Homo sapiens (Human)

Protein length

Gly486-Gly827

Predicted molecular weight

41.62 kDa

Nature

Recombinant

Endotoxin level

Please contact with the lab for this information.

Purity

>90% as determined by SDS-PAGE.

Accession

P11217

Applications

ELISA, Immunogen, SDS-PAGE, WB, Bioactivity testing in progress

Form

Lyophilized

Storage buffer

Lyophilized from a solution in PBS pH 7.4, 0.02% NLS, 1mM EDTA, 4% Trehalose, 1% Mannitol.

Reconstitution

Reconstitute in sterile water for a stock solution. A copy of datasheet will be provided with the products, please refer to it for details.

Shipping

In general, proteins are provided as lyophilized powder/frozen liquid. They are shipped out with dry ice/blue ice unless customers require otherwise.

Stability and Storage

Use a manual defrost freezer and avoid repeated freeze thaw cycles. Store at 2 to 8°C for frequent use. Store at -20 to -80°C for twelve months from the date of receipt.

Alternative Names

Glycogen phosphorylase, muscle form, 2.4.1.1, Myophosphorylase, PYGM

Data Image
  • SDS-PAGE
    SDS-PAGE for Recombinant Human PYGM protein
References

Aerobic exercise acts differentially on proteins from glucose and glycogen pathways in the SOL and PL muscles of offspring rats submitted to a low-protein maternal diet., PMID:39954356

Identify of blood glucose metabolism regulation pathways and related proteins in the db/db mouse model through iTRAQ quantitative mass spectrometry., PMID:39932544

Molecular characterization of AMP-activated protein kinase (AMPK) α1/α2 from Cyprinus carpio and its roles in glucolipid metabolism and immune response., PMID:39920952

Identification of disease-specific extracellular vesicle-associated plasma protein biomarkers for Duchenne Muscular Dystrophy and Facioscapulohumeral Muscular Dystrophy., PMID:39649602

Elucidation of molecular mechanisms, pathways, and diseases modulated by arsenicals through toxogenomics and multi-omics analysis., PMID:39531826

Comprehensive Proteomic Analysis of Dysferlinopathy Unveiling Molecular Mechanisms and Biomarkers Linked to Pathological Progression., PMID:39350328

Biological function and potential application of PANoptosis-related genes in colorectal carcinogenesis., PMID:39237645

Key genes and regulatory networks for diabetic retinopathy based on hypoxia-related genes: a bioinformatics analysis., PMID:39156775

New perspectives for the treatment and follow-up of glycogen storage disease type V: DL-3-hydroxybutyric acid with modified Atkins diet and quadriceps femoris shear wave elastography., PMID:39101220

An autosomal recessive variant in PYGM causes myophosphorylase deficiency in Red Angus composite cattle., PMID:38678201

The importance of muscle glycogen phosphorylase in glial cells function., PMID:38661212

Novel Pathogenic Mutation of P209L in TRPC6 Gene Causes Adult Focal Segmental Glomerulosclerosis., PMID:38315264

A novel genetic model provides a unique perspective on the relationship between postexercise glycogen concentration and increases in the abundance of key metabolic proteins after acute exercise., PMID:38289946

Recurrent atraumatic compartment syndrome as a manifestation of genetic neuromuscular disease., PMID:37919205

Fluoride as a Potential Repressor of Glycogen Metabolism in Skeletal Muscle Cell Line CCL136., PMID:37630316

Distribution of Exonic Variants in Glycogen Synthesis and Catabolism Genes in Late Onset Pompe Disease (LOPD)., PMID:37185710

Exogenous L-lactate administration in rat hippocampus increases expression of key regulators of mitochondrial biogenesis and antioxidant defense., PMID:37008779

"What We Know and What We Do Not Know about Evolutionary Genetic Adaptation to High Altitude Hypoxia in Andean Aymaras"., PMID:36980912

Glycolysis, a new mechanism of oleuropein against liver tumor., PMID:36963367

Brain Homogenate of a Rat Model of Alzheimer's Disease Modifies the Secretome of 3D Cultured Periodontal Ligament Stem Cells: A Potential Neuroregenerative Therapy., PMID:36896321

Proteomics Unveils Post-Mortem Changes in Beef Muscle Proteins and Provides Insight into Variations in Meat Quality Traits of Crossbred Young Steers and Heifers Raised in Feedlot., PMID:36293120

Joint Transcriptome and Metabolome Analysis Prevails the Biological Mechanisms Underlying the Pro-Survival Fight in In Vitro Heat-Stressed Granulosa Cells., PMID:35741360

Transcriptome Reveals Granulosa Cells Coping through Redox, Inflammatory and Metabolic Mechanisms under Acute Heat Stress., PMID:35563749

Identification of Potential Muscle Biomarkers in McArdle Disease: Insights from Muscle Proteome Analysis., PMID:35563042

Integrative Analysis of Nanopore and Illumina Sequencing Reveals Alternative Splicing Complexity in Pig Longissimus Dorsi Muscle., PMID:35480309

Genetic Variants of Glycogen Metabolism Genes Were Associated With Liver PDFF Without Increasing NAFLD Risk., PMID:35464866

Linc-RAM promotes muscle cell differentiation via regulating glycogen phosphorylase activity., PMID:35254536

Proteome basis for the biological variations in color and tenderness of longissimus thoracis muscle from beef cattle differing in growth rate and feeding regime., PMID:35227471

Circulating cardiomyocyte-derived extracellular vesicles reflect cardiac injury during systemic inflammatory response syndrome in mice., PMID:35059851

Transcriptome Profiling Reveals Important Transcription Factors and Biological Processes in Skin Regeneration Mediated by Mechanical Stretch., PMID:34659370

Sequencing refractory regions in bird genomes are hotspots for accelerated protein evolution., PMID:34537008

Kohonen Artificial Neural Network and Multivariate Analysis in the Identification of Proteome Changes during Early and Long Aging of Bovine Longissimus dorsi Muscle Using SWATH Mass Spectrometry., PMID:34523341

Regulation and role of glycophagy in skeletal muscle energy metabolism., PMID:34506219

In vitro fertilization causes excessive glycogen accumulation in mouse placenta., PMID:34418752

Muscle Glycogen Phosphorylase and Its Functional Partners in Health and Disease., PMID:33924466

Generation of the iPSC line IISHDOi007-A from peripheral blood mononuclear cells from a patient with McArdle disease harbouring the mutation c.2392 T > C; p.Trp798Arg., PMID:33370875

Functional and clinical implications of genetic structure in 1686 Italian exomes., PMID:33326653

Dietary carbohydrates influence muscle texture of olive flounder Paralichthys olivaceus through impacting mitochondria function and metabolism of glycogen and protein., PMID:33311521

The etiology of rhabdomyolysis: an interaction between genetic susceptibility and external triggers., PMID:32978841

PYGM mRNA expression in McArdle disease: Demographic, clinical, morphological and genetic features., PMID:32735634

A New Glycogen Storage Disease Caused by a Dominant PYGM Mutation., PMID:32386344

What functional proteomic and biochemical analysis tell us about animal stress in beef?, PMID:32109608

Investigating the genetic susceptibility to exertional heat illness., PMID:32054689

Glucagon regulation of carbohydrate metabolism in rainbow trout: in vivo glucose fluxes and gene expression., PMID:31767730

The effect of muscle glycogen phosphorylase (Pygm) knockdown on zebrafish morphology., PMID:31747538

Bioinformatics-based discovery of PYGM and TNNC2 as potential biomarkers of head and neck squamous cell carcinoma., PMID:31324732

Identification of differentially expressed proteins in the injured lung from zinc chloride smoke inhalation based on proteomics analysis., PMID:30770755

Quantitative proteomics analysis to identify biomarkers of chronic myofascial pain and therapeutic targets of dry needling in a rat model of myofascial trigger points., PMID:30662282

Epidermal growth factor receptor controls glycogen phosphorylase in T cells through small GTPases of the RAS family., PMID:30647127

Retinopathy Associated with Biallelic Mutations in PYGM (McArdle Disease)., PMID:30316539

Datasheet
$ 313
Product specifications
100 μg 313 1 mg 1629

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For research use only. Not for human or drug use.

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Recombinant Human PYGM Protein, N-His [YHC86801]
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