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Amyloid Fibrils antibody
As low as
€600.00
In stock
Ref
00097723
Amyloid monomeric proteins can oligomerize into destructive amyloid fibrils. Amyloidogenic conformations of non-disease related proteins can be created by partial protein misfolding or denaturation.
Many degenerative diseases are known to be related to the accumulation of misfolded proteins as amyloid fibers.
Many degenerative diseases are known to be related to the accumulation of misfolded proteins as amyloid fibers.
| ID Covalab | pab60017 |
|---|---|
| Product type | Primary antibodies |
| Clonality | Polyclonal antibody |
| Raised in | Rabbit |
| Immunogen | Fibrils prepared from human Aβ42 peptide |
| Activity cross reaction | Reacts with epitopes common to many human amyloid fibrils and fibrillar oligomers but not prefibrillar oligomers or natively folded proteins. Predicted to recognize mouse and rat based on sequence homology. |
| Species | Hu, Ms, Rat |
| Labelling | None |
| Form | Purified |
| Preservative | NaN3 0.09% |
| Storage instructions | This product is stable for at least 1 year at -20°C. Freeze in multiple aliquots to avoid repeated freeze-thaw cycles. |
| Target | Amyloid Fibrils |
| Applications | DB, ELISA, IHC, WB |
| Working dilutions | Optimal dilutions should be determined by the end user. The following are guidelines only: WB (1 - 2 µg/ml) DB (0.5 - 1 µg/ml) IHC (1 - 5 µg/ml) ELISA (1 - 10 µg/ml with amyloid fibril-containing samples on the solid phase) |
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