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ELISA Reagents and Buffers

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Phosph-Free Block ELISA Blocking Buffer

Immunochemistry Technologies LLC

Phosph-Free Block ELISA Blocking Buffer is a novel non-protein blocking formulation designed to eliminate interference and nonspecific background noise associated with antibody-coated ELISA formats and sandwich ELISAs.Phosph-Free Block is formulated for ELISAs using alkaline phosphatase detection or for assays with ultra-sensitivity requirements. However, it is appropriate for assays using HRP detection as well. Using inert no…

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Alternative Block ELISA Blocking Buffer

Immunochemistry Technologies LLC

Reduce non specific binding in ELISAs and stabilize proteins with Alternative Block, an all-synthetic ELISA blocking buffer free of proteins and detergents. Alternative Block is a protein-free, detergent-free ELISA blocking buffer. This unique blocking buffer contains a heterogeneous mixture of proprietary blockers and synthetic stabilizers that block the uncoated regions of the microtiter plate without the use of conventiona…

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Monster Block ELISA Blocking Buffer

Immunochemistry Technologies LLC

Reduce non specific binding in ELISAs, address high background issues, and stabilize proteins with Monster Block, a new ELISA blocking buffer utilizing a heterogenous mixture of nonmammalian blocking agents. Monster Block™ provides a high degree of blocking efficiency and protein stabilization through the use of non-mammalian protein blocking agents and stabilizers. The heterogeneous composition of this unique ELISA blocking…

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Quant*Tag Biotin Quantitation Kit

Vector Laboratories Inc.

The Quant*Tag™ Biotin Kit (BDK-2000) is designed to determine the amount of free biotin in solution or the number of biotins attached to nucleic acids, proteins, or other macromolecules. This kit can be used to determine accurately the labeling efficiency of biotin-labeled molecules.

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BIOTINYLATED SECONDARY ANTIBODIES

Vector Laboratories Inc.

Vector Laboratories’ affinity-purified antibodies are of unmatched quality. These antibodies are prepared using proprietary immunization schedules that produce high affinity antibodies. The antibodies are then purified by affinity chromatography, and cross-reactivities that are likely to interfere with specific labeling are removed by solid phase adsorption techniques.

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