Recombinant Rat GAA Protein
Cat.No. : | GAA-2438R |
Product Overview : | Recombinant Rat GAA full length or partial length protein was expressed. |
- Specification
- Gene Information
- Related Products
Source : | Mammalian Cells |
Species : | Rat |
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 Name : | Gaa glucosidase, alpha, acid [ Rattus norvegicus ] |
Official Symbol : | GAA |
Gene ID : | 367562 |
mRNA Refseq : | NM_199118.1 |
Protein Refseq : | NP_954549.1 |
MIM : | |
UniProt ID : | Q6P7A9 |
Products Types
◆ Recombinant Protein | ||
Gaa-3124M | Recombinant Mouse Gaa Protein, Myc/DDK-tagged | +Inquiry |
GAA-2094R | Recombinant Rat GAA Protein, His (Fc)-Avi-tagged | +Inquiry |
GAA-176H | Recombinant Human GAA protein, MYC/DDK-tagged | +Inquiry |
GAA-159H | Recombinant Human GAA Protein, His-tagged | +Inquiry |
GAA-28087TH | Recombinant Human GAA | +Inquiry |
◆ Lysates | ||
GAA-6077HCL | Recombinant Human GAA 293 Cell Lysate | +Inquiry |
◆ Assay kits | ||
Kit-0353 | GAA Activity Colorimetric Assay Kit | +Inquiry |
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.
Inquiry
- Q&As
- Reviews
Q&As (5)
Ask a questionGAA protein is one of several enzymes involved in glycogen metabolism, each playing a specific role in glycogen breakdown.
Enzyme replacement therapy (ERT) and gene therapy are two treatment options available for Pompe disease patients to replace or correct the deficient GAA protein.
GAA protein deficiency is primarily associated with Pompe disease, but there are other glycogen storage diseases related to deficiencies of different enzymes.
ERT involves the infusion of recombinant GAA protein to replace the missing or deficient enzyme in Pompe disease patients.
While GAA protein therapy can improve the symptoms and quality of life for Pompe disease patients, it may not fully reverse the damage caused by the disease.
Customer Reviews (3)
Write a reviewAdditionally, cost-effectiveness, competitive pricing, and bulk purchase options can also be advantageous for researchers working within limited budgets.
The ability to customize the GAA protein variants or modifications offered by the manufacturer is also advantageous, as it allows me to tailor the protein to my specific research objectives.
I appreciate the manufacturer's commitment to maintaining exceptional protein quality standards, which ensures reliable and consistent results in my trials.
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