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Thermo Fisher Scientific PEX19 Polyclonal Antibody
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PEX19 단백질을 인식하는 Thermo Fisher Scientific의 폴리클로날 항체로, WB, IHC, ICC/IF 등 다양한 응용에 적합합니다. 인간, 생쥐, 랫트 반응성이 있으며, 고순도 항원 친화 크로마토그래피로 정제되었습니다. 세포 내 퍼옥시좀 생합성 연구에 유용합니다.
- 카탈로그번호
- PA522129
- 판매단위
- pk
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마지막 업데이트 2025. 08. 03. 오전 12:37
카탈로그 번호 · 상품 설명출고판매가담기
Thermo Fisher Scientific PA522129 PEX19 Polyclonal Antibody 100 ul pk판매 단위 pk ·
재고 확인 필요
721,400원VAT 포함 793,540원
Thermo Fisher Scientific · Thermo Fisher Scientific PEX19 Polyclonal Antibody
Applications
| Application | Tested Dilution | Publications |
|---|---|---|
| Western Blot (WB) | 1:500–1:20,000 | View 3 publications |
| Immunohistochemistry (Paraffin) (IHC (P)) | 1:100–1:1,000 | - |
| Immunocytochemistry (ICC/IF) | 1:100–1:1,000 | - |
Product Specifications
| Specification | Description |
|---|---|
| Species Reactivity | Human, Mouse, Rat |
| Published Species | Not Applicable |
| Host / Isotype | Rabbit / IgG |
| Class | Polyclonal |
| Type | Antibody |
| Immunogen | Recombinant fragment corresponding to amino acids 1–299 of PEX19 (Uniprot ID: P40855) |
| Conjugate | Unconjugated |
| Form | Liquid |
| Concentration | 1.01 mg/mL |
| Purification | Antigen affinity chromatography |
| Storage Buffer | PBS, pH 7, with 20% glycerol |
| Contains | 0.025% ProClin 300 |
| 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_11152064 |
Product Specific Information
- Recommended positive controls: Jurkat, Raji, NCI-H929, K562, THP-1, HL-60, mouse liver, PC-12, Rat-2
- Predicted reactivity: Mouse (91%), Rat (93%), Bovine (95%)
- Store product as a concentrated solution. Centrifuge briefly prior to opening the vial.
Target Information
PEX19 is required for early peroxisomal biogenesis. It functions as a cytosolic chaperone and import receptor for peroxisomal membrane proteins (PMPs). Peroxins (PEXs) are essential for assembling functional peroxisomes.
Peroxisome biogenesis disorders (PBDs) are genetically heterogeneous autosomal recessive diseases with multiple defects in peroxisomal function. Defects in this gene are associated with Zellweger syndrome (ZWS).
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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