GAA ELISA试剂盒
(Glucosidase, Alpha, Acid (GAA))
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].
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6 results :
GAA
适用: 人
Colorimetric
Sandwich ELISA
3.125 ng/mL - 200 ng/mL
Plasma, Serum, Tissue Homogenate
1 image
GAA
适用: 小鼠
Colorimetric
Sandwich ELISA
31.2 pg/mL - 2000 pg/mL
Plasma, Saliva, Serum, Tissue Homogenate, Urine
1 image
GAA
适用: 大鼠
Colorimetric
Sandwich ELISA
0.31 ng/mL - 20 ng/mL
Plasma, Serum, Tissue Homogenate
1 image
GAA
适用: 人
Colorimetric
Sandwich ELISA
0.156 ng/mL - 10 ng/mL
Seminal Plasma, Tissue Homogenate
Aliases for GAA ELISA试剂盒
glucosidase alpha, acid (GAA) ELISA试剂盒glucosidase, alpha, acid (Gaa) ELISA试剂盒
transmembrane and coiled-coil domain family 1 (TMCC1) ELISA试剂盒
glucosidase, alpha; acid (Pompe disease, glycogen storage disease type II) (gaa) ELISA试剂盒
glucosidase alpha, acid (Gaa) ELISA试剂盒
E430018M07Rik ELISA试剂盒
LYAG ELISA试剂盒
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