Immunology

Lyophilized rabbit IgG fraction to human albumin and buffer salts.

Lyophilized rabbit polyclonal antiboody againts human red blood cells. For immunoblotting, immunostaining of acetone-fixed frozen and formalin-fixed, paraffin-embedded tissue sections.

Lyophilized rabbit IgG fraction to mouse IgG (whole molecule) and buffer salts.

Lyophilized rabbit IgG fraction to sheep red blood cells and buffer salts.

Human IgG positive control is lyophilized human IgG positive control with buffers and salts. IgG is a purified antigen.

98% purity by SDS PAGE. No trace of IgA, IgM or non-immunoglobulin serum proteins

Lyophilized monkey IgG with buffers and salts.

Mouse IgG purified from normal mouse serum.

Mouse IgG purified from normal mouse serum.

IgG, rabbit, fluorescein-conjugated

Lyophilized rabbit IgG F(ab’)2 with buffer salts.

Purified rat IgG may be used as a reference antigen, standard, blocking agent, or coating protein in a variety of immunoassays including ELISA, dot immunobinding, western immunoblotting, immunodiffusion, and immunoelectrophoresis. Other applications include starting materials for the preparation of immunogens and solid phase immunoadsorbents. Rat IgG was used as isotype control in flow cytometry and injected into mice to induce tolerance against rat IgG.

IgG/IgM Depleted Human Complement

IgG/IgM Depleted Human Complement

IgG/IgM Depleted Human Complement

IgG/IgM Depleted Human Serum Heat-Inactivated

IgG/IgM Depleted Human Serum Heat-Inactivated

IgG/IgM Depleted Human Serum Heat-Inactivated

IgG/IgM Depleted Human Serum Heat-Inactivated

Mouse IgG1 (K) purified from clarified mouse MOPC 21 ascites using multi-step procedures which may include salt fractionation, gel filtration, ion-exchange chromatography, affinity chromatography and immunoabsorption. The product is dialyzed into 0.02 M TRIS, 0.15 M sodium chloride, pH 8.1, filtered through a 0.22 µm filter and vialed.

[MOPC 21]
Ascites fluid, collected from Balb/c mice which carry plasmacytomas subcutaneously, are clarified by centrifugation and filtration. It is dialyzed, adjusted to yield at least 5 mg of immunoglobulin, then vialed and lyophilized. Clarified ascites are tested for immunoglobulin by immunoelectrophoresis using antisera specific for the particular type and isotype. Approximately 10% of the total protein is immunoglobulin (including trace levels of the host’s immunoglobulins), 80% is albumin, and 10% is complement and other proteins.

From myeloma source, reactive against IgG1 by subclass-specific radial immunodiffusion and ELISA. This product contains 1% IgG2 , IgG3 , and IgG4 .

From myeloma source, reactive against IgG1 by subclass-specific radial immunodiffusion and ELISA. This product contains 1% IgG2 , IgG3 , and IgG4 .

From myeloma source, this product is reactive specific to its subclass by subclass-specific radial immunodiffusion and ELISA. It contains % IgG1 , IgG3 , and IgG4 .

IgG2A (Kappa) UPC 10, mouse myeloma, purified

Mouse IgG2b is purified from clarified mouse MOPC 141 ascites using multi-step procedures which may include salt fractionation, gel filtration, ion-exchange chromatography, affinity chromatography, and immunoabsorption. The product is dialyzed into 0.02 M Tris 0.15M sodium chloride, pH 8.1, filtered through a 0.22 µm filter and vialed.

Mouse IgG2b (j) is purified from clarified mouse MOPC 195 ascites using multi-step procedures which may include salt fractionation, gel filtration, ion-exchange chromatography, affinity chromatography and immunoabsorption. The product is dialyzed into 0.02 M Tris, 0.15 M sodium chloride, pH 8.1, filtered through a 0.22 µm filter and vialed.

Lyophilized Clarified mouse myeloma ascites IgG2b (j) MOPC 195.

Mouse IgG3 (k) is purified from clarified mouse FLOPC 21 ascites using multi-step procedures which may include salt fractionation, gel filtration, ion-exchange chromatography, affinity chromatography and immunoabsorption. The product is dialyzed into 0.02 M Tris, 0.15 M sodium chloride, pH 8.1, filtered through a 0.22 µm filter and vialed.

[MOPC 104E]
These myeloma proteins are purified from ascites by a combination of salt precipitation, ion exchange and bioaffinity chromatography. Purified proteins are dialyzed into 0.02M Tris, 0.14M sodium chloride, pH 8.1. Product is adjusted to 1.0 mg/ml, filtered, vialed, and stored frozen at -70°C. Product is shipped on dry ice.

Immuno-Fluore™ Mounting Medium is a mounting medium for immunofluorescence preparations. A stabilizing agent has been added that inhibits the fading of fluorescence under the influence of ultraviolet light.

Close-fitting covers to minimize gel dehydration. Recessed bottom to prevent scratching on the bench surface. Plate is hydrophilic

IMMUNOGLOBULINS POLYCLONAL ANTIBODY

Product is the lyophilized powder of human lactoferrin and buffer salts. Human lactoferrin is purified from pooled human colostrum using multi-step procedures which may include salt fractionation, gel filtration, ion-exchange chromatography and immunoabsorption.

Formulated for isolation of mononuclear cells from defibrinated or heparinized whole human blood.

Formulated for isolation of mononuclear cells from defibrinated or heparinized whole human blood.

MES SDS Running Buffer for Bis-Tris Gels in Powder (One Pack makes up 1L)

The MP ouchterlony plate is designed for specific but low affinity antisera. Each plate contains 8 ouchterlony patterns consisting of a center well and 6 outer wells. Plates prepared especially for the MP polyclonal antisera to human IgG subclasses

Anti-Human hemoglobin monoclonal antibody from mouse, in 10 mM phosphate buffer, pH 7.4, containing 0.9 % NaCl and 0.02% NaN₃.

MOPS SDS Running Buffer for Bis-Tris Gels in Powder (One Pack makes up 1L)

This Actin (plant-specific) Mouse mAb offers high specificity and potency and consistency against actins expressed by various plants, which has been experimentally validated in Western blotting (WB) and Immunofluorescence (IF) assays.

This α-Tubulin Mouse mAb offers high specificity and potency and consistency against α-Tubulin expressed by human, mouse, and rat species, which has been experimentally validated in Western blotting (WB), Immunohistochemistry (IHC), Immunoprecipitation (IP) and Immunofluorescence (IF) assays.

This β-Tubulin Mouse mAb offers high specificity and potency and consistency against β-Tubulin expressed by human, mouse, rat, hamster, monkey, goat, and Chlamydomonas reinhardtii species, which has been experimentally validated in Western blotting (WB), Immunohistochemistry (IHC), Immunoprecipitation (IP) and Immunofluorescence (IF) assays.

This GAPDH Mouse mAb (High Potency) offers high specificity and potency and consistency against GAPDH expressed by human, mouse, and rat species, which has been experimentally validated in Western blotting (WB), Immunohistochemistry (IHC), and Immunofluorescence (IF) assays.

This Mouse anti-HA-Tag mAb offers high specificity and potency and consistency against HA tag, which has been experimentally validated in Western blotting (WB), Immunoprecipitation (IP), and Immunofluorescence (IF) assays.

This Mouse anti-mCherry-Tag mAb offers high specificity and potency and consistency against mCherry tag, which has been experimentally validated in Western blotting (WB) and Immunofluorescence (IF) assays.

Mouse IL1 beta ELISA Kit, 96 tests

Mouse IL6 ELISA Kit, 96 tests

Mouse Serum(C57BL/6 background) is a pooled preparation obtained from a normal mouse population. Blood is collected from good quality, normal, healthy mice. The serum, pooled and sterile filtered, shows minimal
hemolysis.

Mouse TNF-alpha ELISA Kit, 96 tests