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GenWay/Mouse IL-13 ELISA Kit/GWB-SKR080/96 Tests
2025-05-08
Description:
Short Description: This product is a Sandwich ELISA with a detection method of Colorimetric 450 nm. The Murine IL-13 ELISA Kit allows for the detection and quantification of endogenous levels of natural and/or recombinant Murine IL-13 proteins within the range of 16-1000 pg/ml. The Murine IL-13 ELISA is capable of recognizing both recombinant and naturally produced Murine IL-13 proteins. The antigens listed below were tested at 50 ng/ml and exhibited less than 1% cross reactivity.• Rat IL-13The antigens listed below were tested at 50 ng/ml and did not exhibit significant cross reactivity or interference. • Human IL-4, sIL-4alpha, IL-13, IL-13V• Murine C-10, G-CSF, IFN-gamma, IL-1alpha, IL-1beta, IL-2, IL-3, IL-7, IL-9, IL-10, JE, KC• Rat IL-4, IL-13 (113 aa)Additional Information:
Mouse IL-13 ELISA Kit | ||||||||||||||||||||
Interleukin-13, T-cell activation protein P600 | ||||||||||||||||||||
IL13 | ||||||||||||||||||||
IL | ||||||||||||||||||||
interleukin 13 | ||||||||||||||||||||
16163 | ||||||||||||||||||||
Il-13, IL-13, Interleukin-13, T-cell activation protein P600 | ||||||||||||||||||||
Interleukin-13 | ||||||||||||||||||||
Cytokine. Inhibits inflammatory cytokine production. Synergizes with IL2 in regulating interferon-gamma synthesis. May be critical in regulating inflammatory and immune responses (By similarity). Positively regulates IL31RA expression in macrophages (PubM | ||||||||||||||||||||
P20109 | ||||||||||||||||||||
NP_032381.1 | ||||||||||||||||||||
NM_008355.3 | ||||||||||||||||||||
Mouse | ||||||||||||||||||||
Quantitative Colorimentric Sandwich ELISA | ||||||||||||||||||||
16 pg/mL | ||||||||||||||||||||
16-1,000 pg/mL | ||||||||||||||||||||
16-1000 pg/ml | ||||||||||||||||||||
Cell lysates, sera and plasma | ||||||||||||||||||||
1 x 96-Well Plate or 12 x 8-Well Strips | ||||||||||||||||||||
Refer to Manual | ||||||||||||||||||||
P20109 | ||||||||||||||||||||
The Murine IL-13 ELISA is capable of recognizing both recombinant and naturally produced Murine IL-13 proteins. The antigens listed below were tested at 50 ng/ml and exhibited less than 1% cross reactivity.• Rat: IL-13The antigens listed below were tested at 50 ng/ml and did not exhibit significant cross reactivity or interference.• Human: IL-4, sIL-4α, IL-13, IL-13V• Murine: C-10, G-CSF, IFN-γ, IL-1α, IL-1β, IL-2, IL-3, IL-7, IL-9, IL-10, JE, KC• Rat: IL-4, IL-13 (113 aa) | ||||||||||||||||||||
ELISA | ||||||||||||||||||||
16163 | ||||||||||||||||||||
ELISA Kit. Refer to manual for specific component formats | ||||||||||||||||||||
6 months | ||||||||||||||||||||
4C/6 Months | ||||||||||||||||||||
Mouse | ||||||||||||||||||||
12 x 8-Well Microstrips | ||||||||||||||||||||
The Aviva Murine IL-13 ELISA Kit contains the components necessary for quantitative determination of natural or recombinant mIL-13 concentrations within any experimental sample including cell lysates, serum and plasma. This particular immunoassay utilizes the quantitative technique of a \"Sandwich\" Enzyme-Linked Immunosorbent Assay (ELISA) where the target protein (antigen) is bound in a \"sandwich\" format by the primary capture antibodies coated to each well-bottom and the secondary detection antibodies added subsequently by the investigator. The capture antibodies coated to the bottom of each well are specific for a particular epitope on the Murine IL-13 cytokine while the user-added detection antibodies bind to epitopes on the captured target protein. Amid each step of the procedure, a series of wash steps must be performed to ensure the elimination of non-specific binding between proteins to other proteins or to the solid phase. After incubation and \"sandwiching\" of the target antigen, a peroxidase enzyme is conjugated to the constant heavy chain of the secondary antibody (either covalently or via Avidin/Streptavidin-Biotin interactions), allowing for a colorimetric reaction to ensue upon substrate addition. When the substrate TMB (3, 3’, 5, 5’-Tetramethylbenzidine) is added, the reaction catalyzed by peroxidase yields a blue color that is representative of the antigen concentration. Upon sufficient color development, the reaction can be terminated through addition of Stop Solution (2 N Sulfuric Acid) where the color of the solution will turn yellow. The absorbance of each well can then be read by a spectrophotometer, allowing for generation of a standard curve and subsequent determination of protein concentration. | ||||||||||||||||||||
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4°C/6 Months | ||||||||||||||||||||
Domestic: within 1 week deliveryInternational: 1 week | ||||||||||||||||||||
Research Use Only |
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