Thermo Fisher Scientific PEX19 Recombinant Rabbit Monoclonal Antibody (JE54-93)
PEX19 단백질을 인식하는 토끼 모노클로날 항체로, 인간 시료에 반응합니다. Western blot, IHC, Flow cytometry 등 다양한 응용에 적합합니다. 재조합 형식이며 Protein A로 정제되었습니다. 연구용으로만 사용 가능합니다.
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Applications
| Application | Tested Dilution | Notes |
|---|---|---|
| Western Blot (WB) | 1:500 | |
| Immunohistochemistry (Paraffin) (IHC (P)) | Assay-dependent | |
| Flow Cytometry (Flow) | Assay-dependent |
Product Specifications
| 항목 | 내용 |
|---|---|
| Species Reactivity | Human |
| Host / Isotype | Rabbit / IgG |
| Expression System | HEK293 cells |
| Class | Recombinant Monoclonal |
| Type | Antibody |
| Clone | JE54-93 |
| Immunogen | Recombinant protein within Human PEX19 (aa 1–140) |
| Conjugate | Unconjugated |
| Form | Liquid |
| Concentration | 1 mg/mL |
| Purification | Protein A |
| Storage Buffer | TBS, pH 7.4, with 0.05% BSA, 40% glycerol |
| Contains | 0.05% sodium azide |
| Storage Conditions | Store at 4°C short term. For long term, store at -20°C, avoiding freeze/thaw cycles. |
| Shipping Conditions | Wet ice |
| RRID | AB_2890341 |
Target Information
This gene is necessary for early peroxisomal biogenesis. It acts both as a cytosolic chaperone and as an import receptor for peroxisomal membrane proteins (PMPs). Peroxins (PEXs) are proteins essential for assembling functional peroxisomes. Peroxisomal biogenesis disorders (PBDs) are genetically heterogeneous, autosomal recessive diseases with defects in peroxisome function. Although clinical features vary, cells from all PBD patients exhibit defects in importing peroxisomal matrix proteins. Defects in this gene cause Zellweger syndrome (ZWS).
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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