AGLA
| Species | Cat.# | Product name | Source (Host) | Tag | Protein Length | Price |
|---|---|---|---|---|---|---|
| Zebrafish | AGLA-7697Z | Recombinant Zebrafish AGLA | Mammalian Cell | His |
|
- Involved Pathway
- Protein Function
- Interacting Protein
AGLA involved in several pathways and played different roles in them. We selected most pathways AGLA participated on our site, such as Starch and sucrose metabolism, Metabolic pathways, which may be useful for your reference. Also, other proteins which involved in the same pathway with AGLA were listed below. Creative BioMart supplied nearly all the proteins listed, you can search them on our site.
| Pathway Name | Pathway Related Protein |
|---|---|
| Starch and sucrose metabolism | AMY2A3;TREH;GAA;UGT5G1;GYS2;UGT1A9;UGT1A1;UGT1A2;AGLA |
| Metabolic pathways | UGT1AB;NDUFS5;GLDC;AMPD1;NDST1;PLD2;MOCS1;PIK3C2A;EXT1A |
AGLA has several biochemical functions, for example, 4-alpha-glucanotransferase activity, amylo-alpha-1,6-glucosidase activity, catalytic activity. Some of the functions are cooperated with other proteins, some of the functions could acted by AGLA itself. We selected most functions AGLA had, and list some proteins which have the same functions with AGLA. You can find most of the proteins on our site.
| Function | Related Protein |
|---|---|
| 4-alpha-glucanotransferase activity | AGL;AGLA |
| amylo-alpha-1,6-glucosidase activity | AGL;AGLA |
| catalytic activity | GOT2B;SLC27A1A;SPTLC3;SLC3A2A;PNP5B;AGXTA;PFKMB;PPM1BA;SULF2B |
AGLA has direct interactions with proteins and molecules. Those interactions were detected by several methods such as yeast two hybrid, co-IP, pull-down and so on. We selected proteins and molecules interacted with AGLA here. Most of them are supplied by our site. Hope this information will be useful for your research of AGLA.
- Q&As
- Reviews
Q&As (20)
Ask a questionAGLA deficiency affects kidney function due to glycolipid accumulation.
AGLA research guides diagnosis, treatment, and understanding of lysosomal disorders.
AGLA operates within lysosomes, breaking down glycolipids into simpler molecules.
AGLA's enzymatic deficiency is targeted in treatments for lysosomal disorders.
AGLA deficiency is inherited in an X-linked manner, affecting males more severely.
Deficiency of AGLA causes Fabry disease, characterized by glycolipid buildup.
Yes, AGLA deficiency affects the nervous system due to glycolipid buildup.
AGLA stands for "Alpha-Galactosidase A," involved in breaking down complex sugars.
Fabry disease results from AGLA deficiency, causing glycolipid storage and symptoms.
AGLA deficiency leads to glycolipid accumulation, impacting cellular health.
AGLA participates in lipid metabolism by breaking down glycolipids.
Yes, AGLA deficiency can cause organ damage due to glycolipid accumulation.
Yes, AGLA's deficiency impacts heart health due to glycolipid storage.
Research investigates AGLA's function, deficiency, and therapeutic approaches.
AGLA breaks down glycolipids, preventing their accumulation in cells.
Yes, ongoing research uncovers AGLA's roles, implications, and treatment avenues.
Yes, AGLA deficiency can cause hearing loss due to glycolipid buildup.
AGLA deficiency can affect blood vessel health due to glycolipid buildup.
Enzyme replacement therapy is used to introduce functional AGLA into the body.
Yes, AGLA deficiency affects skin health due to glycolipid accumulation.
Customer Reviews (5)
Write a reviewDespite its price, the protein product’s contributions to our research made it a worthwhile investment.
Replicable outcomes across different cell lines showcased the protein product’s consistency.
Comprehensive documentation eased the integration of the protein product into our workflow.
Consistently obtaining specific outcomes with the protein product validated its importance.
The unique features of the protein product enriched our research endeavors.
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