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Catalog #P1014C1
| Cat # | Size | Price | Quantity | |
|---|---|---|---|---|
| P1014C1 | 25µg | $195.00 | ||
| P1014C1 | 100µg | $395.00 |
| Expression System | CHO |
|---|---|
| Protein Tag | C-His |
| Purity | > 95% by SDS-PAGE under reducing conditions |
| Endotoxin | < 1 EU per ug by the LAL method |
| Activity | Positive |
| Conjugate | Unconjugated |
| Species | Human |
| Accession Number | AAD13932.1 |
| Protein Sequence | Leu23-Thr529 |
| Molecular Weight | The protein has a predicted molecular weight of 60 kDa. The protein migrates at approximately 60-65 kDa on SDS-PAGE with DTT-reduced condition. |
| Formulation | 25mM Tris, 150mM NaCl, pH7.5 |
| Concentration | 25µg size is bottled at 0.2mg/mL concentration. 100 µg and 500 µg size is bottled at lot specific concentration. |
| Purification | Affinity Ni-NTA |
| Applications | ELISA |
| Format | Liquid |
| Reconstitution | NA |
| Shipping Condition | Cold Pack |
| Storage/Shelf Life | An unopened vial can be stored at 4°C for 2 weeks or at -20°C and below for six months. This stock solution should be aliquoted and stored at -70°C to minimize the freeze/thaw cycles. |
| Background Information | The HEXA protein, also known as beta-hexosaminidase subunit alpha, is an enzyme crucial for breaking down gangliosides, particularly GM2, in lysosomes within cells, according to Prospec Protein Specialists and National Institutes of Health (NIH). A deficiency in this enzyme, often caused by mutations in the HEXA gene, leads to Tay-Sachs disease, where GM2 gangliosides accumulate in nerve cells, causing neurological damage. |