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Recombinant Human PGM3 Protein, N-His

Catalog #:   YHB63301 Specific References (49) DATASHEET
Applications: ELISA, Immunogen, SDS-PAGE, WB, Bioactivity testing in progress
Expression system: E. coli
Accession: O95394
Protein length: Met1-Phe542
Overview

Catalog No.

YHB63301

Expression system

E. coli

Species

Homo sapiens (Human)

Protein length

Met1-Phe542

Predicted molecular weight

62.01 kDa

Nature

Recombinant

Endotoxin level

Please contact with the lab for this information.

Purity

>90% as determined by SDS-PAGE.

Accession

O95394

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

Phosphoacetylglucosamine mutase, PAGM, 5.4.2.3, Acetylglucosamine phosphomutase, N-acetylglucosamine-phosphate mutase, Phosphoglucomutase-3, PGM 3, PGM3, AGM1

Data Image
  • SDS-PAGE
    SDS-PAGE for Recombinant Human PGM3 protein
References

Fluorescence melting curve analysis for genotyping of c.1396G > A (rs473267) of phosphoglucomutase-3 gene., PMID:40409221

Targeting PGM3 abolishes SREBP-1 activation-hexosamine synthesis feedback regulation to effectively suppress brain tumor growth., PMID:40249802

Direct detection of 3-nitrotyrosine reveals the nitration of proteins in laboratory exposure and ambient aerosols., PMID:40246517

Hyper IgE Syndrome: Bridging the Gap Between Immunodeficiency, Atopy, and Allergic Diseases., PMID:40082265

PGM3 insufficiency: a glycosylation disorder causing a notable T cell defect., PMID:39776909

Rapid identification of primary atopic disorders (PAD) by a clinical landmark-guided, upfront use of genomic sequencing., PMID:39381601

Effects of L-Leu-L-Leu peptide on growth, proliferation, and apoptosis in broiler intestinal epithelial cells., PMID:38457989

Tumor-Associated and Systemic Autoimmunity in Pre-Clinical Breast Cancer among Post-Menopausal Women., PMID:38002248

Hyper IgE syndrome-related disease treated with dupilumab: A case report., PMID:37720709

The role of glycosylation in clinical allergy and immunology., PMID:37717626

A Systematic Review of Polycyclic Aromatic Hydrocarbon Derivatives: Occurrences, Levels, Biotransformation, Exposure Biomarkers, and Toxicity., PMID:37703436

ERBIN and phosphoglucomutase 3 deficiency., PMID:37369151

Multitranscript analysis reveals an effect of 2-deoxy-d-glucose on gene expression linked to unfolded protein response and integrated stress response in primary human monocytes and monocyte-derived macrophages., PMID:37290716

PGM3 inhibition shows cooperative effects with erastin inducing pancreatic cancer cell death via activation of the unfolded protein response., PMID:37260977

Multi-Omics Profiling in PGM3 and STAT3 Deficiencies: A Tale of Two Patients., PMID:36768728

Proteomics and bioinformatics analysis of cardiovascular related proteins in offspring exposed to gestational diabetes mellitus., PMID:36277748

Severe Protein Loss in a 6-month-old Exclusively Breastfed Infant with Atopic Dermatitis., PMID:36254543

A novel variant in GNPNAT1 gene causing a spondylo-epi-metaphyseal dysplasia resembling PGM3-Desbuquois like dysplasia., PMID:36097642

RELA∙8-Oxoguanine DNA Glycosylase1 Is an Epigenetic Regulatory Complex Coordinating the Hexosamine Biosynthetic Pathway in RSV Infection., PMID:35883652

PGM3 regulates beta-catenin activity to promote colorectal cancer cell progression., PMID:35723049

A De Novo Cause of PGM3 Deficiency Treated with Hematopoietic Stem Cell Transplantation., PMID:35040011

Targeting PGM3 as a Novel Therapeutic Strategy in KRAS/LKB1 Co-Mutant Lung Cancer., PMID:35011738

Profound differences in IgE and IgG recognition of micro-arrayed allergens in hyper-IgE syndromes., PMID:34653276

Skeletal and Bone Mineral Density Features, Genetic Profile in Congenital Disorders of Glycosylation: Review., PMID:34441372

Inborn errors of IL-6 family cytokine responses., PMID:34044328

Promyelocytic Leukemia Antigen Expression: a Histological Marker for Primary Biliary Cholangitis Diagnosis?, PMID:33850801

Dust exposure and pulmonary inflammation in Standardbred racehorses fed dry hay or haylage: A pilot study., PMID:33840486

Two Novel Homozygous Mutations in Phosphoglucomutase 3 Leading to Severe Combined Immunodeficiency, Skeletal Dysplasia, and Malformations., PMID:33534079

Heterozygous PGM3 Variants Are Associated With Idiopathic Focal Epilepsy With Incomplete Penetrance., PMID:33193641

Novel PGM3 compound heterozygous variants with IgE-related dermatitis, lymphopenia, without syndromic features., PMID:33098103

The Child with Elevated IgE and Infection Susceptibility., PMID:32830295

Hexosamine pathway inhibition overcomes pancreatic cancer resistance to gemcitabine through unfolded protein response and EGFR-Akt pathway modulation., PMID:32235891

Compound Heterozygous PGM3 Mutations in a Thai Patient with a Specific Antibody Deficiency Requiring Monthly IVIG Infusions., PMID:31707513

Clinical Utility Gene Card for: PGM3 defective congenital disorder of glycosylation., PMID:31231132

CDG and immune response: From bedside to bench and back., PMID:31095764

Detection of 3-Nitrotyrosine in Atmospheric Environments via a High-performance Liquid Chromatography-electrochemical Detector System., PMID:30774123

Defective glycosylation leads to defective gp130-dependent STAT3 signaling in PGM3-deficient patients., PMID:30578875

The clinical and mechanistic intersection of primary atopic disorders and inborn errors of growth and metabolism., PMID:30565252

An Update on Syndromes with a Hyper-IgE Phenotype., PMID:30466772

Hyper IgE syndromes: clinical and molecular characteristics., PMID:30264496

Eleven percent intact PGM3 in a severely immunodeficient patient with a novel splice-site mutation, a case report., PMID:30157810

Human hyper-IgE syndrome: singular or plural?, PMID:30094507

Hyper-IgE in the allergy clinic--when is it primary immunodeficiency?, PMID:30043993

Multiplexed detection of DOCK8, PGM3 and STAT3 proteins for the diagnosis of Hyper-Immunoglobulin E syndrome using gold nanoparticles-based immunosensor array platform., PMID:30005381

The effect of geographical and climatic properties on grass pollen and Phl p 5 allergen release., PMID:29626255

Inhibition of the Hexosamine Biosynthetic Pathway by targeting PGM3 causes breast cancer growth arrest and apoptosis., PMID:29515119

Sequence-structure relationships, expression profiles, and disease-associated mutations in the paralogs of phosphoglucomutase 1., PMID:28837627

A founder mutation underlies a severe form of phosphoglutamase 3 (PGM3) deficiency in Tunisian patients., PMID:28704707

A Novel PGM3 Mutation Is Associated With a Severe Phenotype of Bone Marrow Failure, Severe Combined Immunodeficiency, Skeletal Dysplasia, and Congenital Malformations., PMID:28543917

Datasheet
$ 313
Product specifications
100 μg 313 1 mg 1629

Contact Information

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Distributor list

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

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Recombinant Human PGM3 Protein, N-His [YHB63301]
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