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GAA Antibody / Glucosidase alpha acid

GAA Antibody / Glucosidase alpha acid is available 1 time from Njs poly labs

R32608 | GAA Antibody / Glucosidase alpha acid size: 0.1mg | 449.08 USD

Catalog number R32608
Supplier NJS poly
Price 449.08 USD
Size 0.1mg
1. Gene info
Synonyms gene name
  • glucosidase, alpha; acid
Discovery year1986-01-01
Havana BLAST/BLATOTTHUMG00000177537
MeSH Data
Tree numbers
  • E05.196.401.143
  • E05.301.300.096
  • E05.478.566.320.200
  • E05.601.262
  • E05.601.470.320.200
Category Antibody
Concentration 0.5mg/ml if reconstituted with 0.2ml sterile DI water
Form Antigen affinity purified
Conjugation Unconjugated
Clone Polyclonal antibody
Recognised antigen GAA / Glucosidase alpha acid
Host animal Rabbit (Oryctolagus cuniculus)
Clonality Polyclonal (rabbit origin)
Species reactivity Human (Homo sapiens), Rat ; Due to limited knowledge and inability to test the antibody against all known species, we cannot guarantee that no other cross reactivity can occur.
Tested applications WB, IHC-P
Recommended dilutions Western blot: 0.5-1ug/ml,Immunohistochemistry (FFPE): 1-2ug/ml
Notes Optimal dilution of the GAA antibody should be determined by the researcher.
Added buffer Lyophilized from 1X Phosphate Buffered Saline (PBS) with 2.5% BSA and 0.025% sodium azide
Intented use This GAA antibodyis to be used only for research purposes and not for diagnostics..
Uniprot # P10253
Purity Antigen affinity
Description Lysosomal alpha-glucosidase is an enzyme that in humans is encoded by the GAA gene. 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.
Immunogen Amino acids 494-527 (TALAWWEDMVAEFHDQVPFDGMWIDMNEPSNFIR-human) were used as the immunogen for the GAA antibody.
Storage After reconstitution, the GAA antibody may be kept for up to one month refrigerated at +4 degrees C.For long-term, aliquot and store at -20 deg. Celcius or lower. Cycles of freezing and thawing can denaturate the peptide chains of the antibodies and reduce their sensitivity and/or change their affinity. Prepare aliqotes in such a manner so that freeze-thaw cycles are minimized. Avoid repeated freezing and thawing.
Localization Cytoplasmic, membranous
Additional description The GAA Antibody / Glucosidase alpha acid is a α- or alpha protein sometimes glycoprotein present in blood.
Properties If you buy Antibodies supplied by NJS poly they should be stored frozen at - 24°C for long term storage and for short term at + 5°C.
French translation anticorps
Gene targetGAA Glucosidase alpha acid
Short name GAA Antibody / Glucosidase alpha acid
Technique Antibody
Alternative name GAA (Antibody to) / Glucosidase a acid
Alternative technique antibodies
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GAA Antibody / Glucosidase alpha acid size: 0.1mg
EU:+32-(0)1-658-90-45 US:+1-(408)780-0908 [email protected]
  • GAA
  • Glucosidase
  • alpha
  • acid
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