Recombinant Zebrafish AGLA

• Cat.No.: AGLA-7697Z
• Product Overview: Recombinant Zebrafish AGLA full length or partial length protein was expressed.

Specification

• Source: Mammalian Cells
• Species: Zebrafish
• Tag: His
• Form: Liquid or lyophilized powder
• Endotoxin: < 1.0 eu per μg of the protein as determined by the LAL method.
• Purity: >80%
• Notes: This item requires custom production and lead time is between 5-9 weeks. We can custom produce according to your specifications.
• Storage: Store it at +4 oC for short term. For long term storage, store it at -20 oC～-80 oC.
• Storage Buffer: PBS buffer

Gene Information

• Gene Name: agla amylo-alpha-1, 6-glucosidase, 4-alpha-glucanotransferase a [ Danio rerio (zebrafish) ]
• Official Symbol: AGLA
• Gene ID: 567798
• mRNA Refseq: NM_001172653
• Protein Refseq: NP_001166124
• UniProt ID: X1WFT9

Reviews

08/26/2021

 Despite its price, the protein product’s contributions to our research made it a worthwhile investment.

04/15/2020

 Replicable outcomes across different cell lines showcased the protein product’s consistency.

08/23/2019

 Comprehensive documentation eased the integration of the protein product into our workflow.

03/11/2019

 Consistently obtaining specific outcomes with the protein product validated its importance.

10/13/2016

 The unique features of the protein product enriched our research endeavors.

Q&As

How does AGLA's activity impact kidney function?

AGLA deficiency affects kidney function due to glycolipid accumulation.

What are the applications of AGLA research?

AGLA research guides diagnosis, treatment, and understanding of lysosomal disorders.

What's the role of AGLA in lysosomes?

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

Can AGLA be used as a therapeutic target?

AGLA's enzymatic deficiency is targeted in treatments for lysosomal disorders.

How is AGLA deficiency inherited?

AGLA deficiency is inherited in an X-linked manner, affecting males more severely.

Can AGLA deficiency lead to diseases?

Deficiency of AGLA causes Fabry disease, characterized by glycolipid buildup.

Can AGLA deficiency impact the nervous system?

Yes, AGLA deficiency affects the nervous system due to glycolipid buildup.

What is the AGLA protein?

AGLA stands for "Alpha-Galactosidase A," involved in breaking down complex sugars.

What's the connection between AGLA and Fabry disease?

Fabry disease results from AGLA deficiency, causing glycolipid storage and symptoms.

How does AGLA's deficiency affect cell function?

AGLA deficiency leads to glycolipid accumulation, impacting cellular health.

How does AGLA contribute to lipid metabolism?

AGLA participates in lipid metabolism by breaking down glycolipids.

Can AGLA deficiency lead to organ damage?

Yes, AGLA deficiency can cause organ damage due to glycolipid accumulation.

Can AGLA's role extend to heart health?

Yes, AGLA's deficiency impacts heart health due to glycolipid storage.

How is AGLA's role studied?

Research investigates AGLA's function, deficiency, and therapeutic approaches.

How is AGLA's function significant?

AGLA breaks down glycolipids, preventing their accumulation in cells.

Is AGLA research ongoing?

Yes, ongoing research uncovers AGLA's roles, implications, and treatment avenues.

Can AGLA deficiency lead to hearing loss?

Yes, AGLA deficiency can cause hearing loss due to glycolipid buildup.

How does AGLA's dysfunction impact blood vessels?

AGLA deficiency can affect blood vessel health due to glycolipid buildup.

How is AGLA's activity restored in treatment?

Enzyme replacement therapy is used to introduce functional AGLA into the body.

Can AGLA deficiency impact skin health?

Yes, AGLA deficiency affects skin health due to glycolipid accumulation.