GAA Polyclonal Antibody | G-AB-11801
Gentaur Antibodies
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Gentaur Antibodies
GAA Polyclonal Antibody | G-AB-11801
- SKU:
- G-AB-11801
- Availability:
- 3 to 5 Working Days
- Host:
- Rabbit
- Reactivity:
- Human, Mouse, Rat
GAA Polyclonal Antibody | G-AB-11801 | Gentaur Antibodies
Overview: This gene encodes lysosomal alpha-glucosidase, which is essential for the degradation of glycogen to glucose in lysosomes. The encoded preproprotein is proteolytically processed to generate multiple intermediate forms and the mature form of the enzyme. 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. Alternative splicing results in multiple transcript variants.
Category Type: Polyclonal Antibody
Research Areas: Cancer, Metabolism, Signal Transduction
Synonyms: GAA, LYAG
Reactivity: Human, Mouse, Rat
Host: Rabbit
Isotype: IgG
Gene ID: 2548
Accession #:
Clonality:
Immunogen: A synthetic peptide of human GAA (NP_000143.2) .
Clone #:
Conjugation: Unconjugated
Swissprot: P10253
Santa Cruz:
Calculated MW: 105 kDa
Observed MW: 105 kDa
Concentration: 1 mg/mL
Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3
Purification method: Affinity purification
Application: WB
Dilution: WB 1:500-1:2000
Storage: Store at -20°C. Avoid freeze / thaw cycles.
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