Thermo Fisher Scientific PEX19 Polyclonal Antibody
PEX19 단백질을 인식하는 Thermo Fisher Scientific의 Rabbit Polyclonal Antibody로, WB, IHC, ICC/IF에 사용 가능. 인간, 마우스, 랫트 반응성. 고순도 친화성 정제, 액상 형태로 -20°C 보관. 세포 내 퍼옥시솜 생합성 연구에 적합.
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- PA5102781
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- pk
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Applications
| Application | Tested Dilution |
|---|---|
| Western Blot (WB) | 1:500–1:2,000 |
| Immunohistochemistry (Paraffin) (IHC (P)) | 1:50–1:200 |
| Immunocytochemistry (ICC/IF) | 1:100–1:500 |
Product Specifications
| Specification | Detail |
|---|---|
| Species Reactivity | Human, Mouse, Rat |
| Host / Isotype | Rabbit / IgG |
| Class | Polyclonal |
| Type | Antibody |
| Immunogen | A synthesized peptide derived from human PEX19 (Accession P40855), corresponding to amino acid residues Y218–L268 |
| Conjugate | Unconjugated |
| Form | Liquid |
| Concentration | 1 mg/mL |
| Purification | Affinity chromatography |
| Storage Buffer | PBS, pH 7.4, with 50% glycerol |
| Contains | 0.02% sodium azide |
| Storage Conditions | -20°C |
| Shipping Conditions | Wet ice |
| RRID | AB_2852172 |
Product Specific Information
Antibody detects endogenous levels of total PEX19.
Target Information
PEX19 is essential for early peroxisomal biogenesis. It functions as both a cytosolic chaperone and an import receptor for peroxisomal membrane proteins (PMPs). Peroxins (PEXs) are required for assembling functional peroxisomes. Defects in this gene are associated with peroxisome biogenesis disorders (PBDs), a group of autosomal recessive diseases characterized by impaired peroxisomal matrix protein import. Mutations can cause Zellweger syndrome (ZWS).
For Research Use Only.
Not for use in diagnostic procedures. Not for resale without express authorization.
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