Thermo Fisher Scientific HSP60 Polyclonal Antibody
HSP60 단백질을 인식하는 Rabbit Polyclonal Antibody로 다양한 종(Human, Mouse, Rat 등)에 반응. WB, IHC, ICC/IF 등 다중 응용 가능. 높은 특이성과 안정성, 연구용으로 적합. 장기 보관 시 -20°C에서 안정적으로 유지.
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Applications
| Application | Tested Dilution | Publications |
|---|---|---|
| Western Blot (WB) | 1:5,000–1:20,000 | View 1 publication |
| Immunohistochemistry (IHC) | – | View 1 publication |
| Immunohistochemistry (Paraffin) (IHC (P)) | 1:100–1:1,000 | – |
| Immunocytochemistry (ICC/IF) | 1:100–1:1,000 | View 1 publication |
Product Specifications
| Specification | Description |
|---|---|
| Species Reactivity | Hamster, Human, Mouse, Rat |
| Published Species | Human |
| Host / Isotype | Rabbit / IgG |
| Class | Polyclonal |
| Type | Antibody |
| Immunogen | Recombinant fragment corresponding to a region within amino acids 205–483 of HSP60 (Uniprot ID: P10809) |
| Conjugate | Unconjugated |
| Form | Liquid |
| Concentration | 0.3 mg/mL |
| Purification | Antigen affinity chromatography |
| Storage Buffer | PBS, pH 7, with 20% glycerol, 1% BSA |
| Contains | 0.025% ProClin 300 |
| Storage Conditions | Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles. |
| Shipping Conditions | Wet ice |
| RRID | AB_2552112 |
Product Specific Information
- Recommended positive controls: 293T, A431, HeLa, HepG2, mouse brain, rat brain
- Predicted reactivity: Mouse (97%), Rat (97%), Zebrafish (85%), Xenopus laevis (91%), Pig (99%), Chicken (94%), Rhesus Monkey (97%), Chimpanzee (99%), Bovine (98%)
- Store product as a concentrated solution. Centrifuge briefly prior to opening the vial.
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 region functions as a bidirectional promoter between two related family members. Several pseudogenes are associated with this gene. Two transcript variants encoding the same protein have been identified. Mutations 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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