Recombinant Human AGL protein(731-830 aa), C-His-tagged
Cat.No. : | AGL-2739H |
Product Overview : | Recombinant Human AGL protein(P35573)(731-830 aa), fused with C-terminal His tag, was expressed in E. coli. |
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Source : | E. coli |
Species : | Human |
Tag : | His |
Protein length : | 731-830 aa |
Form : | 0.15 M Phosphate buffered saline |
AASequence : | AVTRHSPSIHQSVVAVSRTAFRNPK TSFYSKEVPQMCIPGKIEEVVLEAR TIERNTKPYRKDENSINGTPDITVE IREHIQLNESKIVKQAGVATKGPNE |
Storage : | Shipped on dry ice. Avoid repeated freeze-thaw cycles. Upon receipt, 2 days when stored at 2 to 8 °C after thawing. Up to 12 months when aliquoted and stored at -20 to -80°C. |
Reconstitution : | It is recommended that sterile water be added to the vial to prepare a stock solution of 0.2 ug/ul. Centrifuge the vial at 4°C before opening to recover the entire contents. |
Gene Name : | AGL amylo-alpha-1, 6-glucosidase, 4-alpha-glucanotransferase [ Homo sapiens ] |
Official Symbol : | AGL |
Synonyms : | AGL; amylo-alpha-1, 6-glucosidase, 4-alpha-glucanotransferase; amylo 1, 6 glucosidase, 4 alpha glucanotransferase; glycogen debranching enzyme; glycogen storage disease type III; glycogen debrancher; amylo-1, 6-glucosidase, 4-alpha-glucanotransferase; GDE; |
Gene ID : | 178 |
mRNA Refseq : | NM_000028 |
Protein Refseq : | NP_000019 |
MIM : | 610860 |
UniProt ID : | P35573 |
Products Types
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◆ Lysates | ||
AGL-8980HCL | Recombinant Human AGL 293 Cell Lysate | +Inquiry |
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Related Gene
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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Customer Reviews (5)
Write a reviewNotable improvements in cell proliferation were attributed to the protein product’s efficacy.
We observed a significant enhancement in enzyme activity using the protein product.
The protein product’s compatibility with various assays broadened the scope of our investigations.
Reliable protein-protein interaction studies were enabled by the protein product’s pure composition.
Minimal background noise in our assays indicated the protein product’s quality.
Q&As (20)
Ask a questionYes, AGL mutations can cause low blood sugar levels due to impaired glucose release.
AGL mutations might contribute to cardiomyopathy due to glycogen accumulation.
Yes, AGL mutations can lead to muscle weakness due to impaired glycogen breakdown.
Research explores whether AGL's function is conserved in different organisms.
AGL activity ensures proper glycogen breakdown, maintaining cellular glycogen levels.
Yes, ongoing research uncovers AGL's roles in metabolism and related diseases.
AGL's enzymatic activity alters glycogen structure by removing branches.
AGL's role in glycogen metabolism makes it a potential therapeutic target.
AGL's enzymatic role is in breaking down glycogen, not synthesizing it.
AGL dysfunction can affect various tissues due to glycogen storage disruptions.
AGL deficiency affects muscle cells due to impaired glycogen breakdown.
Research on AGL provides insights into glycogen metabolism and related diseases.
Yes, hormones regulate AGL activity to maintain glucose levels.
Yes, AGL's role in glycogen breakdown can impact heart function and health.
AGL's role in glycogen breakdown helps maintain glucose homeostasis.
Yes, AGL deficiency is usually inherited in an autosomal recessive manner.
AGL deficiency hinders glucose release from glycogen, affecting energy supply.
Yes, AGL mutations can impact exercise tolerance due to limited energy supply.
Yes, AGL mutations can impact multiple organs due to glycogen storage issues.
AGL mutations can impact brain health due to glycogen storage issues in certain tissues.
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