GBA Polyclonal Antibody
| Dodavatel: | Reddot Biotech USA Inc. | |||||||||||||||||||
| Teplota skladování: | Store at -20°C. Avoid freeze / thaw cycles. | |||||||||||||||||||
| Katalogové číslo: |
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This is a GBA Polyclonal Antibody from Reddot Biotech. This product is for Research Use Only.
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.
| Clonality | Polyclonal | |
| Purification Method | Antigen affinity purification | |
| Isotype | IgG | |
| Host | Rabbit | |
| Immunogen | Synthetic peptide of human GBA | |
| Swissprot | P04062 | |
| Calculated MW | 60 kDa | |
| Observed MW | Refer to figures | |
| Gene Accession | NP000148 | |
| Reactivity | Human,Mouse | |
| Applications | WB,IHC,ELISA | |
| Conjugation | Unconjugated | |
| Dilution | WB 1:500-1:2000, IHC 1:50-1:100, ELISA 1:5000-1:10000 | |
| Concentration | 1.56 mg/mL | |
| Buffer | PBS with 0.05% NaN3 and 40% Glycerol, pH7.4 |
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