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Recombinant Aspergillus Niger AGLB Protein (21-443 aa), His-tagged

Cat.No. : AGLB-1629A
Product Overview : Recombinant Aspergillus Niger (strain CBS 513.88/FGSC A1513) AGLB Protein (21-443 aa) is produced by Yeast expression system. This protein is fused with a 6xHis tag at the N-terminal. Protein Description: Full Length of Mature Protein.
  • Specification
  • Gene Information
  • Related Products
Description : Hydrolyzes a variety of simple alpha-D-galactoside as well as more complex molecules such as oligosaccharides and polysaccharides.
Source : Yeast
Species : Aspergillus Niger
Tag : His
Form : Tris-based buffer,50% glycerol
Molecular Mass : 48.7 kDa
Protein length : 21-443 aa
AA Sequence : DGVGRTPALGWNSWNAYSCDIDADK IVTAANEVVNLGLKDLGYEYINIDD CWSVKSGRNTTTKRIIPDPDKFPNG ISGVADQVHALGLKLGIYSSAGLTT CAGYPASLGYEEIDAQSFAEWGIDY LKYDNCGVPTNLTDQYTYCVPDSTD GSNYPNGTCVNLTDAAPQGYDWATS TTAKRYQRMRDALLSVNRTILYSLC DWGQADVNAWGNATGNSWRMSGDIT ATWSRIAEIANENSFLMNYANFWGY PDPDMLEVGNGNLTLPENRAHFALW AMMKAPLIIGTPLDSIDTSHLTILS NKPLLTFHQDAVIGRPAYPYKWGYN PDWTFDPEHPAEYWSGPTSSGEVFV LMLNSEGEVKTRSAVWEEVPELKDR GTKKNSKEKKGFKVTDAWTGKDLGC VKDKYEVKLQAHDVAVLVVGGQC
Purity : > 90% as determined by SDS-PAGE.
Notes : Repeated freezing and thawing is not recommended. Store working aliquots at 4 centigrade for up to one week.
Storage : The shelf life is related to many factors, storage state, buffer ingredients, storage temperature and the stability of the protein itself. Generally, the shelf life of liquid form is 6 months at -20 centigrade/-80 centigrade. The shelf life of lyophilized form is 12 months at -20 centigrade/-80 centigrade.
Concentration : A hardcopy of COA with reconstitution instruction is sent along with the products.
Synonyms : aglB; Melibiase B;
UniProt ID : A2QEJ9
Synonyms : aglB; Melibiase B;
UniProt ID : A2QEJ9

For Research Use Only. Not intended for any clinical use. No products from Creative BioMart may be resold, modified for resale or used to manufacture commercial products without prior written approval from Creative BioMart.

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Q&As (20)

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Can AGALB's deficiency be targeted for therapies? 11/30/2022

Research explores potential therapeutic approaches for managing AGALB deficiency.

How does AGALB dysfunction impact blood vessels? 07/19/2022

AGALB deficiency can affect blood vessel health due to glycolipid accumulation.

How is AGALB's enzymatic activity studied? 06/23/2022

Research investigates AGALB's role, enzymatic activity, and potential therapies.

How is AGALB deficiency treated? 06/23/2021

Treatment involves managing symptoms and complications of Schindler disease.

How is AGALB's function important? 01/31/2021

AGALB breaks down glycolipids, preventing their buildup in cells.

Can AGALB deficiency lead to joint problems? 12/06/2020

Yes, AGALB deficiency can result in joint issues due to glycolipid accumulation.

How does AGALB contribute to lipid metabolism? 10/23/2020

AGALB is crucial in lipid metabolism by breaking down glycolipids.

How does AGALB contribute to lysosomal degradation? 04/06/2020

AGALB plays a pivotal role in lysosomal degradation of glycolipids.

Can AGALB deficiency affect nervous system health? 03/16/2020

Yes, AGALB deficiency impacts the nervous system due to glycolipid buildup.

How does AGALB's deficiency affect cell health? 02/28/2020

AGALB deficiency results in glycolipid buildup, impacting cellular function.

What's the role of AGALB in lysosomes? 10/26/2019

AGALB operates within lysosomes, breaking down glycolipids into simpler molecules.

Can AGALB's role extend to skin health? 04/25/2019

Yes, AGALB's deficiency can impact skin health due to glycolipid storage.

Can AGALB deficiency impact digestive processes? 03/03/2019

Yes, AGALB deficiency affects digestion due to its role in breaking down complex sugars.

What are the clinical manifestations of Schindler disease? 11/21/2018

Schindler disease symptoms can include neurological and systemic issues.

What's the connection between AGALB and Schindler disease? 07/22/2018

Schindler disease is caused by AGALB mutations, leading to glycolipid storage and symptoms.

How is AGALB deficiency inherited? 12/12/2017

AGALB deficiency is inherited in an autosomal recessive manner.

Can AGALB mutations lead to diseases? 10/24/2017

Mutations in AGALB cause Schindler disease, characterized by glycolipid accumulation.

Can AGALB deficiency lead to organ damage? 05/27/2017

Yes, AGALB deficiency can result in organ damage due to glycolipid accumulation.

Is AGALB research ongoing? 05/08/2017

Yes, ongoing research uncovers AGALB's roles, disease mechanisms, and potential therapies.

How is AGALB deficiency diagnosed? 10/29/2016

Diagnosis involves measuring AGALB activity in blood or genetic testing.

Customer Reviews (5)

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Reviews
02/25/2020

     The product’s efficacy in promoting specific cellular responses underscored its importance.

    06/23/2019

       Replicating results underscored the reliability and significance of the protein product.

      11/13/2018

        Consistency in the product’s performance fortified the reliability of our experimental conclusions.

        07/15/2018

           The protein product’s innovative features enabled exploration of novel cellular mechanisms.

          04/26/2018

             Utilizing the product led to a reliable enhancement in enzyme activity, confirming its impact.

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