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alpha-Glucosidase Assay Kit

Cat.No. : Kit-0062
Product Overview : alpha-Glucosidase Assay Kit is a colorimetric kinetic determination of a-Glucosidase activity.
  • Specification
  • Gene Information
  • Related Products
Applications : Direct Assays: α-glucosidase activity in biological samples.Characterization and Quality Control for α-glucosidase production.Drug Discovery: high-throughput screen and evaluation of α-glucosidase inhibitors.
Storage : Store all reagents at -20°C. Shelf life: 6 months after receipt.

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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How does AGLU contribute to cellular homeostasis? 08/26/2022

AGLU's role in glycogen breakdown helps maintain cellular glucose levels.

How does AGLU's activity impact energy availability? 05/16/2022

AGLU's activity provides glucose for energy needs in cells.

How does AGLU deficiency affect muscle cells? 02/18/2022

AGLU deficiency affects muscle cells due to glycogen accumulation.

How does AGLU's activity impact cellular energy? 09/18/2021

AGLU's activity provides glucose for cellular energy production.

Is AGLU research ongoing? 11/16/2020

Yes, ongoing research explores AGLU's roles, implications, and potential therapies.

How does AGLU's role relate to metabolic pathways? 09/29/2020

AGLU participates in metabolic pathways by breaking down glycogen.

How is AGLU's structure characterized? 04/25/2020

AGLU has a specific protein structure that supports its enzymatic function.

Can AGLU's enzymatic activity be restored? 08/31/2019

Enzyme replacement therapy aims to restore AGLU's activity in Pompe disease.

Can AGLU be targeted for therapeutic interventions? 06/08/2019

AGLU's deficiency is targeted in Pompe disease treatments to restore enzyme activity.

Can AGLU deficiency lead to diseases? 06/24/2018

Deficiency of AGLU causes Pompe disease, characterized by glycogen accumulation.

What's the role of AGLU in carbohydrate metabolism? 05/07/2018

AGLU breaks down complex carbohydrates into simpler sugars like glucose.

How is AGLU linked to Pompe disease? 03/16/2018

Pompe disease results from AGLU deficiency, causing glycogen buildup and symptoms.

How does AGLU contribute to glycogen breakdown? 10/17/2017

AGLU plays a key role in breaking down glycogen, releasing glucose for energy.

Can AGLU deficiency affect infantile-onset Pompe disease? 10/04/2017

Yes, infantile-onset Pompe disease is characterized by severe AGLU deficiency.

Can AGLU's activity be regulated? 07/21/2017

Yes, AGLU's activity can be influenced by hormones and metabolic signals.

Can AGLU deficiency impact liver health? 06/21/2017

Yes, AGLU deficiency can affect liver health due to glycogen accumulation.

How does AGLU's dysfunction lead to Pompe disease? 11/02/2016

AGLU deficiency causes glycogen to accumulate, leading to muscle and organ issues.

How does AGLU's deficiency impact glycogen storage? 07/29/2016

AGLU deficiency leads to abnormal glycogen storage, causing tissue damage.

Can AGLU's deficiency affect respiratory muscles? 06/24/2016

Yes, AGLU deficiency can lead to respiratory muscle weakness in Pompe disease.

Can AGLU deficiency impact heart health? 01/08/2016

Yes, AGLU deficiency affects heart health due to glycogen buildup.

Customer Reviews (5)

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Reviews
09/24/2021

    The protein product’s consistent outcomes supported the reproducibility of our studies.

    01/31/2019

       Compatibility across diverse assays expanded our research possibilities significantly.

      06/17/2018

        AGLU interactions were effectively modulated by the protein product, broadening our understanding.

        02/19/2018

           Employing the product across multiple cell types consistently yielded comparable results.

          12/09/2016

            The product’s contributions to our insights justified its cost and return on investment.

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