IHC buffers - Quenching - AP

IHC buffers - Quenching - AP


Chromogenic detection methods often use a conjugated enzyme to visualize epitope-antibody interactions. When using this method of detection, the endogenous activity of the same enzyme must be blocked. For example, protocols that include horseradish peroxidase (HRP) or alkaline phosphatase (AP) may require reagents to prevent non-specific signals. Tissues such as kidney, liver, or vascular areas with red blood cells, contain endogenous peroxidase activity. Peroxidase blocking reagents formulated with 3-10% H2O2 can be used to prevent endogenous peroxidase from cleaving the substrate. Endogenous AP found in intestine, kidney, lymphoid and other tissue can be blocked with 1 mM Levamisole. The intestinal form of AP is unaffected by Levamisole but can be blocked by using 1% acetic acid.

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Descripción
Cond.
Precio Sin IVA
orb320484-5g
 5g 
orb134393-100mg
 100mg 
orb134393-1g
 1g 
orb134393-250mg
 250mg 
orb1225990-50mg
 50mg 
orb320484-10g
 10g 
orb1225990-200mg
 200mg 
orb1310146-500mg
 500mg 
orb1225990-25mg
 25mg 
orb1225990-100mg
 100mg 
orb1225990-10mg
 10mg 
orb1904052-500mg
 500mg 
259114-10mg
 10mg 
259114-100mg
 100mg 
002311-5mg
 5mg 
259114-50mg
 50mg 
285166-10mg
 10mg 
018241-10mg
 10mg 
285166-5mg
 5mg 
285166-100mg
 100mg