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Recombinant Human B3GAT3 Protein, N-His

Catalog #:   YHB42801 Specific References (25) DATASHEET
Applications: ELISA, Immunogen, SDS-PAGE, WB, Bioactivity testing in progress
Expression system: E. coli
Accession: O94766
Protein length: Leu74-Val335
Overview

Catalog No.

YHB42801

Expression system

E. coli

Species

Homo sapiens (Human)

Protein length

Leu74-Val335

Predicted molecular weight

31.34 kDa

Nature

Recombinant

Endotoxin level

Please contact with the lab for this information.

Purity

>90% as determined by SDS-PAGE.

Accession

O94766

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

Galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase 3, Beta-1,3-glucuronyltransferase 3, GlcUAT-I, Glucuronosyltransferase I, GlcAT-I, B3GAT3, UDP-GlcUA:Gal beta-1,3-Gal-R glucuronyltransferase

Data Image
  • SDS-PAGE
    SDS PAGE for recombinant Human B3GAT3 protein
References

Sulfated glycosaminoglycans are host epithelial cell targets of the Candida albicans toxin candidalysin., PMID:39285260

Prenatal and neonatal phenotype of Larsen of La Réunion Island syndrome (B4GALT7-linkeropathy)., PMID:38705458

Metabolic Cardiomyopathies and Cardiac Defects in Inherited Disorders of Carbohydrate Metabolism: A Systematic Review., PMID:37239976

Investigation of Copy Number Variation in South African Patients With Congenital Heart Defects., PMID:36205932

SLC35B2 Acts in a Dual Role in the Host Sulfation Required for EV71 Infection., PMID:35420441

Severe phenotypes of B3GAT3-related disorder caused by two heterozygous variants: a case report and literature review., PMID:35151321

Glycogenes in Oncofetal Chondroitin Sulfate Biosynthesis are Differently Expressed and Correlated With Immune Response in Placenta and Colorectal Cancer., PMID:34966741

B3GAT3-related linkeropathy and an in-frame homozygous deletion in an adult patient., PMID:34537402

Identification of Potentially Related Genes and Mechanisms Involved in Skeletal Muscle Atrophy Induced by Excessive Exercise in Zebrafish., PMID:34439993

Chikungunya Virus Strains from Each Genetic Clade Bind Sulfated Glycosaminoglycans as Attachment Factors., PMID:32999033

Pseudodiastrophic dysplasia expands the known phenotypic spectrum of defects in proteoglycan biosynthesis., PMID:31988067

Further Defining the Phenotypic Spectrum of B3GAT3 Mutations and Literature Review on Linkeropathy Syndromes., PMID:31438591

The clinical and mutational spectrum of B3GAT3 linkeropathy: two case reports and literature review., PMID:31196143

High Expression B3GAT3 Is Related with Poor Prognosis of Liver Cancer., PMID:30847403

Role of heparan sulfate in the Zika virus entry, replication, and cell death., PMID:30684694

B3GAT3-related disorder with craniosynostosis and bone fragility due to a unique mutation., PMID:28771243

Genome-Wide Screening Uncovers the Significance of N-Sulfation of Heparan Sulfate as a Host Cell Factor for Chikungunya Virus Infection., PMID:28404855

Functional validation of novel compound heterozygous variants in B3GAT3 resulting in severe osteopenia and fractures: expanding the disease phenotype., PMID:27871226

Abnormal Proteoglycan Synthesis Due to Gene Defects Causes Skeletal Diseases with Overlapping Phenotypes., PMID:27871115

A homozygous B3GAT3 mutation causes a severe syndrome with multiple fractures, expanding the phenotype of linkeropathy syndromes., PMID:26086840

Skeletal dysplasia in a consanguineous clan from the island of Nias/Indonesia is caused by a novel mutation in B3GAT3., PMID:25893793

Skeletal dysplasia, global developmental delay, and multiple congenital anomalies in a 5-year-old boy-report of the second family with B3GAT3 mutation and expansion of the phenotype., PMID:24668659

On the roles and regulation of chondroitin sulfate and heparan sulfate in zebrafish pharyngeal cartilage morphogenesis., PMID:22869369

Attachment of Chlamydia trachomatis L2 to host cells requires sulfation., PMID:22675117

Faulty initiation of proteoglycan synthesis causes cardiac and joint defects., PMID:21763480

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 B3GAT3 Protein, N-His [YHB42801]
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