anti- Alpha galactosidase A antibody

Embark on a journey into the world of lysosomal storage disorders with our specialized Anti-Alpha Galactosidase A Polyclonal Antibody, now available in a convenient 100µg size. Alpha galactosidase A is a pivotal enzyme involved in the degradation of glycosphingolipids, and its deficiency leads to Fabry disease, a rare genetic disorder. Our meticulously crafted polyclonal antibody offers exceptional specificity and sensitivity, making it an ideal choice for a wide range of applications, from enzyme kinetics studies to immunofluorescence assays.

What truly distinguishes our Anti-Alpha Galactosidase A Polyclonal Antibody is its exceptional performance. It has undergone rigorous validation and testing to ensure consistent and reproducible results, effectively reducing experimental variability and saving valuable time and resources.

With a generous 100µg size, this product provides an ideal balance between cost-effectiveness and practicality, offering ample antibody for multiple experiments while minimizing wastage, aligning with our commitment to sustainable research practices.

Engineered for user-friendliness, our Anti-Alpha Galactosidase A Polyclonal Antibody is suitable for researchers of all experience levels, from newcomers to seasoned scientists. It seamlessly integrates into various laboratory techniques, enhancing the accuracy and dependability of your experiments.

Contribute to a deeper understanding of rare diseases and enzymology with confidence, knowing you have the support of a high-quality, meticulously crafted Anti-Alpha Galactosidase A Polyclonal Antibody. Advance your research and be part of groundbreaking discoveries in the field.

Product Name

Alpha galactosidase A antibody

Size

100µg

Form

liquid

Purification

Immunogen affinity purified

Purity

≥95% as determined by SDS-PAGE

Host

Rabbit

Clonality

polyclonal

Isotype

IgG

Storage

PBS with 0.02% sodium azide and 50% glycerol pH 7.3, -20℃ for 12 months(Avoid repeated freeze / thaw cycles.)

BACKGROUND

GLA, also named as Melibiase, Agalsidas and Alpha-galactosidase A, Belongs to the glycosyl hydrolase 27 family. It hydrolysis of terminal, non-reducing alpha-D-galactose residues in alpha-D-galactosides, including galactose oligosaccharides, galactomannans and galactolipids. Fabry disease is an X-linked lysosomal storage disorder resulting from the deficient activity of GLA. Enzyme replacement therapy(ERT) with GLA is currently the most effective therapeutic strategy for patients with Fabry disease, a lysosomal storage disease.

IMMUNOGEN INFORMATION

Immunogen

galactosidase, alpha

Synonyms

Alpha galactosidase A, galactosidase, alpha

Observed MW

49 kDa

APPLICATION

Tested Application

ELISA, IHC, IP, WB

Recommended Dilution

WB: 1:500-1:5000; IHC: 1:20-1:200; IP: 1:500-1:5000

UNIPROT INFORMATION

UniProt ID

P06280

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