beta 2-Microglobulin ELISA Kit (Human) (OKIA00054)
|Datasheets/Manuals||Click here to download product manual. As variation between lots may occur, always reference the lot-specific manual received with each kit.|
|Predicted Species Reactivity||Human|
|Product Format||In Solution|
|Application||Enzyme-linked Immunosorbent assay-Sandwich|
|ELISA Kit Detection Method||Colorimetric, OD450 nm|
|ELISA Kit Duration||130 Minutes|
|ELISA Kit Principle||Aviva Systems Biology beta 2-Microglobulin ELISA Kit (Human) (OKIA00054) is based on standard sandwich enzyme-linked immuno-sorbent assay technology. An antibody for Beta-2-microglobulin has been pre-coated onto a 96-wellplate (12 x 8 Well Strips). Standards or test samples are added to the wells, incubated and washed to remove unbound proteins. An Anti-Beta-2-microglobulin - HRP conjugated detector antibody is then added, incubated and unbound conjugate is washed away. An enzymatic reaction is produced through the addition of TMB substrate which is catalyzed by HRP generating a blue color product that changes to yellow after adding acidic stop solution. The density of yellow coloration read by absorbance at 450 nm is quantitatively proportional to the amount of sample Beta-2-microglobulin captured in the well.|
|ELISA Kit Range||3.125 ng/ml - 100 ng/ml|
|ELISA Kit Component|
|Additional Information||Intended Use: 1. DILUENT CONCENTRATE (Running Buffer)One bottle containing 50 ml of a 5X concentrated diluent running buffer. 2. WASH SOLUTION CONCENTRATE One bottle containing 50 ml of a 20X concentrated wash solution.3. ENZYME-ANTIBODY CONJUGATE 100XOne vial containing 150 ul of affinity purified anti-Human Beta 2-Microglobulin antibody conjugated with horseradish peroxidase in a stabilizing buffer.4. CHROMOGEN-SUBSTRATE SOLUTIONOne vial containing 12 mL of 3,3’,5,5’-tetramethybenzidine (TMB) and hydrogen peroxide in citric acid buffer at pH 3.3.5. STOP SOLUTIONOne vial containing 12 ml 0.3 M sulfuric acid.WARNING: Avoid contact with skin.6. ANTI-HUMAN B2M ELISA MICRO PLATETwelve removable eight (8) well micro well strips in well holder frame. Each well is coated with affinity purified anti-Human B2M.7. HUMAN B2M CALIBRATOROne vial containing a lyophilized Human Beta 2-Microglobulin calibrator.|
1. DILUENT CONCENTRATE (Running Buffer)
One bottle containing 50 ml of a 5X concentrated diluent running buffer.
2. WASH SOLUTION CONCENTRATE
One bottle containing 50 ml of a 20X concentrated wash solution.
3. ENZYME-ANTIBODY CONJUGATE 100X
One vial containing 150 ul of affinity purified anti-Human Beta 2-Microglobulin antibody conjugated with horseradish peroxidase in a stabilizing buffer.
4. CHROMOGEN-SUBSTRATE SOLUTION
One vial containing 12 mL of 3,3’,5,5’-tetramethybenzidine (TMB) and hydrogen peroxide in citric acid buffer at pH 3.3.
5. STOP SOLUTION
One vial containing 12 ml 0.3 M sulfuric acid.
WARNING: Avoid contact with skin.
6. ANTI-HUMAN B2M ELISA MICRO PLATE
Twelve removable eight (8) well micro well strips in well holder frame. Each well is coated with affinity purified anti-Human B2M.
7. HUMAN B2M CALIBRATOR
One vial containing a lyophilized Human Beta 2-Microglobulin calibrator.
|Reconstitution and Storage||Store as indicated in product manual.|
|Sample Type||Serum, plasma and other biological fluids|
|Predicted Homology Based on Immunogen Sequence||Human|
|Assay Info||Assay Methodology: Quantitative Sandwich ELISA|
|Gene Full Name||beta-2-microglobulin|
|NCBI Gene Id||567|
|Description of Target||Component of the class I major histocompatibility complex (MHC). Involved in the presentation of peptide antigens to the immune system. Exogenously applied M.tuberculosis EsxA or EsxA-EsxB (or EsxA expressed in host) binds B2M and decreases its export to the cell surface (total protein levels do not change), probably leading to defects in class I antigen presentation.|
- Reconstitution & Storage Instructions
- Western Blotting/Immunoblotting (WB/IB) Protocol
- Immunohistochemistry (IHC) Protocol
- Immunocytochemistry (ICC) Protocol
- Enzyme-Linked ImmunoSorbent Assay (ELISA) Protocol
- Blocking Peptide Competition Protocol (BPCP)
- Immunoprecipitation (IP) Protocol
- Antibody Array (AA) Protocol
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