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Anti-GAA Polyclonal Antibody
Catalog No. TMAB-06240 Copy Product Info
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Anti-GAA Polyclonal Antibody is a Rabbit antibody targeting GAA. Anti-GAA Polyclonal Antibody can be used in IHC-P,IHC-Fr,IF.
Anti-GAA Polyclonal Antibody
Copy Product Info🥰Excellent
Catalog No. TMAB-06240
Anti-GAA Polyclonal Antibody is a Rabbit antibody targeting GAA. Anti-GAA Polyclonal Antibody can be used in IHC-P,IHC-Fr,IF.
Anti-GAA Polyclonal Antibody
| Pack Size | Price | USA Stock | Global Stock | Quantity |
|---|---|---|---|---|
| 50 μL | $220 | 7-10 days | 7-10 days | |
| 100 μL | $373 | 7-10 days | 7-10 days | |
| 200 μL | $527 | 7-10 days | 7-10 days |
For In stock only · Estimated delivery: USA Stock (1-2 days) Global Stock (5-7 days)
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For research use only—not for human use. No sales to individuals. Use as intended only.
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Product Introduction
Bioactivity
Antigen Details
Chemical Properties
Stability & Storage
| Description | Anti-GAA Polyclonal Antibody is a Rabbit antibody targeting GAA. Anti-GAA Polyclonal Antibody can be used in IHC-P,IHC-Fr,IF. |
| Ig Type | IgG |
| Reactivity | Mouse (predicted:Human,Rat,Dog,Pig,Horse,Sheep) |
| Verified Activity | Paraformaldehyde-fixed, paraffin embedded (Mouse testis); Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15 min; Block endogenous peroxidase by 3% hydrogen peroxide for 20 minutes; Blocking buffer (normal goat serum) at 37°C for 30 min; Antibody incubation with (GAA) Polyclonal Antibody, Unconjugated (TMAB-06240) at 1:400 overnight at 4°C, followed by a conjugated Goat Anti-Rabbit IgG antibody for 90 minutes, and DAPI for nuclei staining. |
| Application | |
| Recommended Dose | IHC-P: 1:100-500; IHC-Fr: 1:100-500; IF: 1:200-800 |
| Antibody Type | Polyclonal |
| Host Species | Rabbit |
| Subcellular Localization | Lysosome. Lysosome membrane. |
| Construction | Polyclonal Antibody |
| Purification | Protein A purified |
| Appearance | Liquid |
| Formulation | 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol. |
| Concentration | 1mg/ml |
| Research Background | This gene encodes acid alpha-glucosidase, which is essential for the degradation of glycogen to glucose in lysosomes. Different forms of acid alpha-glucosidase are obtained by proteolytic processing. Defects in this gene are the cause of glycogen storage disease II, also known as Pompe's disease, which is an autosomal recessive disorder with a broad clinical spectrum. Three transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008]. |
| Immunogen | KLH conjugated synthetic peptide: human GAA/Glucosidase alpha |
| Antigen Species | Human |
| Gene Name | GAA |
| Gene ID | |
| Protein Name | Lysosomal alpha-glucosidase |
| Uniprot ID | |
| Function | Essential for the degradation of glygogen to glucose in lysosomes.
Subcellular Location : Lysosome. Lysosome membrane. |
| Molecular Weight | Theoretical: 83/92/98 kDa. |
| Stability & Storage | Store at 2°C-8°C for 1 month. Store at -20°C or -80°C for 12 months. Avoid repeated freeze-thaw cycles. |
| Transport | Shipping with blue ice. |
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