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General description
This gene encodes a lysosomal membrane protein that cleaves the beta-glucosidic linkage of glycosylceramide, an intermediate in glycolipid metabolism. Mutations in this gene cause Gaucher disease, a lysosomal storage disease characterized by an accumulation of glucocerebrosides. A related pseudogene is approximately 12 kb downstream of this gene on chromosome 1. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2010]
Immunogen
A synthesized peptide derived from human Glucosylceramidase beta (Glucosylceramidase beta (GBA))
Physical form
Buffer: PBS with 0.02% sodium azide,0.05% BSA,50% glycerol,pH7.3.
| biological source | rabbit |
| Quality Segment | 100 |
| conjugate | unconjugated |
| antibody product type | primary antibodies |
| clone | monoclonal |
| form | liquid |
| species reactivity | mouse, rat |
| concentration | 0.51 mg/mL |
| technique(s) | western blot: 1:500-1:2000 |
| UniProt accession no. | P04062 |
| shipped in | wet ice |
| storage temp. | −20°C |
| target post-translational modification | unmodified |
| Gene Information | human ... GBA(2629) |
| 长度(mm) | |
| 宽度(mm) | |
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| 重量(kg) |
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¥ 1451.54
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¥ 4039.86
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¥ 5887.85
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¥ 1956.41
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¥ 6894.69
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¥ 4390.38
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¥ 2842.54
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¥ 2666.57
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¥ 1476.00
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¥ 1509.00
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¥ 2277.64
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