Protein Method Blocking Buffers
Biotang Inc BLOTTO/Tween 20 in TBS (with azide), 250 ml
BLOTTO/Tween 20 in TBS (with azide), 250 ml.
Biotang Inc GELATIN- Blocking Buffer in PBS (with azide), 500 ml
GELATIN- Blocking Buffer in PBS (with azide), 500 ml.
Biotang Inc CASEIN- Blocking Buffer in PBS (with azide), 250 ml
CASEIN- Blocking Buffer in PBS (with azide), 250 ml.
Biotang Inc GELATIN- Blocking Buffer in TBS (with azide), 500 ml
GELATIN- Blocking Buffer in TBS (with azide), 500 ml.
Bioworld Blotto/Tween in PBS, 250 mL
Blotto/Antifoam in PBS Blot blocking buffer used to block non-specific binding site for antibodies on the membrane Technical Information: 5% nonfat dry milk, 0.05% Tween, 0.02% Sodium azide in PBS
AbD Serotec 5x ELISA Coating Buffer, 500mL
A specialist coating buffer for use in all ELISA formats. Designed to stabilize the tertiary structure of the antibody or antigen and maximize adsorption onto polystyrene plates. It is especially effective in sandwich ELISA, preserving the antigen recognition regions of the coating antibody, allowing greater binding reactivity.
Bioworld Blotto in TBS, 1 L
Blotto in TBS Blot blocking buffer used to block non-specific binding for antibodies on the membrane Technical Information: 5% nonfat dry milk, 0.02% Sodium azide in TBS
Bioworld Casein-Blocking Buffer in TBS w/ Azide, 1 L
Product DescriptionCasein-blocking buffer is 3% in TBS with 0.02% sodium azide. It is a liquid used for Western blots and ELISA. Buffer used for blocking excess binding sites on membranes and microplates in antibody-based detection methods.
INNOVEX BIOSCIENCES IMMUNODILUENT & BLOCK WITH GREEN COLOR INDICATOR 125 ML
Immunodiluent& Block 125ml MFCD00131855
Santa Cruz Biotechnology Tris Buffered Saline with Tween 20: 1 L of 20X, 1 L
Tris Buffered Saline with Tween 20: 1 L of 20X is a high-quality 20X concentrate for dilution to a 1X working solution commonly used as a wash solution for western blot membranes and microtiter plate wells in ELISA assays. Tris Buffered Saline with Tween 20 (TBST) is an optimal formulation of pH stabilizers, salts and detergents designed to effectively remove excess material from the microtiter plate wells without disrupting the ELISA binding reaction. By maintaining the proper buffering environment, unbound components can be washed away without suppressing antigen-antibody binding interactions, thereby reducing nonspecific background and increasing the specific signal.
