This gene encodes a member of the glycosyl hydrolase 2 family. The encoded protein localizes to the lysosome where it is the final exoglycosidase in the pathway for N-linked glycoprotein oligosaccharide catabolism. Mutations in this gene are associated with beta-mannosidosis, a lysosomal storage disease that has a wide spectrum of neurological involvement. [provided by RefSeq, Jul 2008]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| MANBABA-20-REGO | 20 (40 μL) | 200 μL |
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| MANBABA-20-REGR | 20 (40 μL) | 200 μL |
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| MANBABA-20-ORGR | 20 (40 μL) | 200 μL |
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| MANBABA-20-GOGR | 20 (40 μL) | 200 μL |
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| MANBABA-20-GRRE | 20 (40 μL) | 200 μL |
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| MANBABA-20-GROR | 20 (40 μL) | 200 μL |
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| MANBABA-20-GRGO | 20 (40 μL) | 200 μL |
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| MANBABA-20-AQOR | 20 (40 μL) | 200 μL |
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This gene encodes a member of the glycosyl hydrolase 2 family. The encoded protein localizes to the lysosome where it is the final exoglycosidase in the pathway for N-linked glycoprotein oligosaccharide catabolism. Mutations in this gene are associated with beta-mannosidosis, a lysosomal storage disease that has a wide spectrum of neurological involvement. [provided by RefSeq, Jul 2008]
Gene Symbol : MANBA
Gene Name : Mannosidase beta
Chromosome : CHR 4: 102,760,997-102,631,485
Locus : 4q24
Alt. Genes : OPTN
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