Thermo Fisher Scientific HSP60 (Heat Shock Protein 60) Recombinant Rabbit Monoclonal Antibody (HSPD1, 6498R)
HSP60 단백질을 인식하는 Thermo Fisher Scientific의 재조합 토끼 단클론 항체. Western blot 및 IHC(P) 실험에 최적화. HEK293 세포 발현, Protein A/G 정제, PBS 기반 저장. 다양한 종에 반응하며 연구용으로 적합.
- 카탈로그번호
- 3329-RBM15-P1
- 판매단위
- pk
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Thermo Fisher Scientific HSP60 (Heat Shock Protein 60) Recombinant Rabbit Monoclonal Antibody (HSPD1, 6498R)
Applications and Tested Dilution
| Application | Tested Dilution |
|---|---|
| Western Blot (WB) | 1–2 µg/mL |
| Immunohistochemistry (Paraffin) (IHC (P)) | 1–2 µg/mL |
Product Specifications
| 항목 | 내용 |
|---|---|
| Species Reactivity | Bovine, Dog, Chicken, Hamster, Human, Mouse, Non-human primate, Sheep, Pig, Rabbit, Rat |
| Host / Isotype | Rabbit / IgG |
| Expression System | HEK293 cells |
| Class | Recombinant Monoclonal |
| Type | Antibody |
| Clone | HSPD1, 6498R |
| Immunogen | Recombinant human full-length HSP60 protein |
| Conjugate | Unconjugated |
| Form | Liquid |
| Concentration | 200 µg/mL |
| Purification | Protein A/G |
| Storage Buffer | PBS, pH 7.4, with 0.05% BSA |
| Contains | 0.05% sodium azide |
| Storage Conditions | 4°C |
| Shipping Conditions | Ambient (domestic); Wet ice (international) |
Product Specific Information
- Immunohistochemistry (PFA fixed): incubate antibody for 30 min at room temperature.
- Staining of formalin-fixed tissues requires heating tissue sections in 10 mM Tris with 1 mM EDTA, pH 9.0, for 45 min at 95°C, followed by cooling at room temperature for 20 min.
Target Information
This gene encodes a member of the chaperonin family. The encoded mitochondrial protein may function as a signaling molecule in the innate immune system. It is essential for the folding and assembly of newly imported proteins in the mitochondria. The gene is adjacent to a related family member, and the region between the two genes functions as a bidirectional promoter. Several pseudogenes have been associated with this gene. Two transcript variants encoding the same protein have been identified. Mutations in this gene cause autosomal recessive spastic paraplegia 13.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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