Horses

Suitable for immunomicroscopy and flow cytometry or FACS analysis as well as other antibody based fluorescent assays requiring lot-to-lot consistency. This product is designed for immunofluorescence microscopy, fluorescence based plate assays

Horseradish peroxidase is used for production of peroxidase conjugated antisera. It is a widely used label for immunoglobulins in many different immunochemistry applications including ELISA, immunoblotting, and immunohistochemistry.

This product has been assayed against 1.0 &microg of Horse IgG in a standard capture ELISA using pNPP p-nitrophenyl phosphate code # NPP-10 as a substrate for 30 minutes at room temperature.

This product has been assayed against 1.0 ug of Horse IgG in a standard capture ELISA using Peroxidase Conjugated Streptavidin #S000-03 and ABTS (2,2'-azino-bis-[3-ethylbenthiazoline-6-sulfonic acid]) code # ABTS-100 as a substrate for 30 minutes a

AntiHorserdh Peroxidase(HRP)Biotin,(Poly,Rabbit IgG)100ug

Anti-Horse Albumin,Texas Red,(Poly,rabbit IgG)3mg

Product Type : Elisa Kit Size : 96 Wells Species : Horse Assay Principle : Quantitative Measurement : Sandwich Target Name : Interleukin 1&beta Sample Type : serum, plasma, Urine, tissue homogenates, cell culture supernates Sensitivity : 0.1ng/ml

Product Type : Elisa Kit Size : 96 Wells Species : Horse Assay Principle : Quantitative Measurement : Sandwich Target Name : Interleukin 1&alpha Sample Type : serum, plasma, Urine, tissue homogenates, cell culture supernates Sensitivity : 10 pg/ml D

Whole IgG antibodies are isolated as intact molecules from antisera by immunoaffinity chromatography. They have an Fc portion and two antigen binding Fab portions joined together by disulfide bonds and therefore they are divalent.

Whole IgG antibodies are isolated as intact molecules from antisera by immunoaffinity chromatography. They have an Fc portion and two antigen binding Fab portions joined together by disulfide bonds and therefore they are divalent.

Whole IgG antibodies are isolated as intact molecules from antisera by immunoaffinity chromatography. They have an Fc portion and two antigen binding Fab portions joined together by disulfide bonds and therefore they are divalent.

Whole IgG antibodies are isolated as intact molecules from antisera by immunoaffinity chromatography. They have an Fc portion and two antigen binding Fab portions joined together by disulfide bonds and therefore they are divalent.