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IL-7 ELISA Kit

IL7 Reactivity: Mouse Colorimetric Sandwich ELISA 15.6-1000 pg/mL Cell Culture Cells, Plasma, Serum
Catalog No. ABIN1112657
  • Target See all IL-7 (IL7) ELISA Kits
    IL-7 (IL7) (Interleukin 7 (IL7))
    Reactivity
    • 5
    • 5
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Mouse
    Detection Method
    Colorimetric
    Method Type
    Sandwich ELISA
    Detection Range
    15.6-1000 pg/mL
    Minimum Detection Limit
    15.6 pg/mL
    Application
    ELISA
    Purpose
    For quantitative detection of IL-7 in mouse serum, plasma or cell.
    Sample Type
    Cell Culture Cells, Plasma, Serum
    Analytical Method
    Quantitative
    Sensitivity
    < 1 pg/mL
    Components
    1. One 96-well plate pre-coated with anti-mouse IL-7 antibody 2. Lyophilized Mouse IL-7 standards: 2 tubes (10ng / tube) 3. Sample / Standard diluent buffer: 30ml 4. Biotin conjugated anti-Mouse IL-7 antibody (Concentrated): 130 µl.
    Material not included
    1. 37 °C incubator 2. Microplate reader (wavelength: 450nm) 3. Precise pipette and disposable pipette tips 4. Automated plate washer 5. ELISA shaker 6. 1.5ml of Eppendorf tubes 7. Plate cover 8. Absorbent filter papers 9. Plastic or glass container with volume of above 1L
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  • Comment

    This kit was based on sandwich enzyme-linked immune-sorbent assay technology. Anti-IL-7 polyclonal antibody was pre-coated onto 96-well plates. And the biotin conjugated anti-IL-7 polyclonal antibody was used as detection antibodies. The standards test samples and biotin conjugated detection antibody were added - the wells subsequently and wash with wash buffer. Avidin-Biotin-Peroxidase Complex was added and unbound conjugates were washed away with wash buffer. TMB substrates were used - visualize HRP enzymatic reaction. TMB was catalyzed by HRP - produce a blue color product that changed into yellow after adding acidic stop solution. The density of yellow is proportional - the IL-7 amount of sample captured in plate. Read the O.D. absorbance at 450 nm in a microplate reader and then the concentration of IL-7 can be calculated.

    Plate
    Pre-coated
    Reagent Preparation
    1. Before the experiment, centrifuge each kit component for several minutes to bring down all reagents to the bottom of tubes. 2. It is recommend to measure each standard and sample in duplicate. 3. Do NOT let the plate completely dry at any time! Since the dry condition can inactivate the biological material on the plate. 4. Do not reuse pipette tips and tubes to avoid cross contamination. 5. Do not use the expired components and the components from different batches. 6. To avoid the marginal effect of plate incubation for temperature differences (the marginal wells always get stronger reaction), it is recommend to equilibrate the ABC working solution and TMB substrate for at least 30 min at room temperature (37°C ) before adding to wells.The TMB substrate (Kit Component 8) is colorless and transparent before use, if not, please contact us for replacement.
    Sample Preparation

    Preparation of sample and reagents 1. Sample Isolate the test samples soon after collecting, then, analyze immediately (within 2 hours). Or aliquot and store at -20 °C for long term. Avoid multiple freeze-thaw cycles.
    Cell: Lyse cells thoroughly, centrifuge at 10000-14000 X g for 3-5 min, collect supernatant, analyze immediately or aliquot and store at -20 °C.
    Serum: Coagulate the serum at room temperature (about 2 hours). Centrifuge at approximately 2000 × g for 20 min. Analyze the serum immediately or aliquot and store at -20 °C .
    Plasma: Collect plasma with heparin or EDTA as the anticoagulant. Centrifuge for 20 min at 2000 x g within 30 min of collection. Analyze immediately or aliquot and store frozen at -20 °C. Citrate can not be used as anticoagulant here. Note: 1. Coagulate blood samples completely, then, centrifuge, and avoid hemolysis and particle. 2. NaN3 can not be used as test sample preservative, since it is the inhibitor for HRP.

    Restrictions
    For Research Use only
  • Preservative
    Sodium azide, Thimerosal (Merthiolate)
  • Target See all IL-7 (IL7) ELISA Kits
    IL-7 (IL7) (Interleukin 7 (IL7))
    Alternative Name
    IL-7 (IL7 Products)
    Synonyms
    IL7 ELISA Kit, IL-7 ELISA Kit, A630026I06Rik ELISA Kit, Il-7 ELISA Kit, hlb368 ELISA Kit, interleukin 7 ELISA Kit, IL7 ELISA Kit, Il7 ELISA Kit
    Background
    Interleukin 7(IL-7) is a hematopoietic growth factor secreted by stromal cells in the red marrow and thymus. It is also produced by keratinocytes, dendritic cells, hepatocytes, neurons, and epithelial cells. IL-7 is a cytokine important for B and T cell development. This cytokine and the hepatocyte growth factor (HGF) form a heterodimer that functions as a pre-pro-B cell growth-stimulating factor. This cytokine is found to be a cofactor for V(D)J rearrangement of the T cell receptor beta (TCRß) during early T cell development. Il-7 promotes hematological malignacies (acute lymphoblastic leukemia, T cell lymphoma), and the elevated levels of IL-7 have also been detected in the plasma of HIV-infected patients.
    Pathways
    JAK-STAT Signaling
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