Human DLL1 ELISA Pair Set

Details for Product No. ABIN2010329, Supplier: Log in to see
Antigen
  • X-delta-1
  • XDelta1
  • Xdelta-1
  • delta
  • delta-1
  • delta1
  • x-delta
  • DLL1
  • CRLM2
  • Ly114
  • Tpte2
  • Tslpr
  • DELTA1
  • DL1
  • Delta
  • Delta1
  • delta-like 1
  • delta-like 1 (Drosophila)
  • cytokine receptor-like factor 2
  • dll1
  • DLL1
  • Crlf2
  • Dll1
Reactivity
Human
Host
Mouse
Conjugate
HRP
Method Type
Sandwich ELISA
Application
ELISA
Options
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Purpose The Human DLL1 ELISA Pair Set is for the quantitative determination of Human DLL1.
This ELISA Pair Set contains the basic components required for the development of sandwich ELISAs.
Detection Method Colorimetric
Sensitivity 46.875 pg/mL
Characteristics Capture Antibody: 0.4 mg/mL of mouse anti-DLL1 monoclonal antibody. Dilute to a working concentration of 2.0 μg/mL in CBS before coating.

Detection Antibody: 0.5 mg/mL mouse anti-DLL1 monoclonal antibody conjugated to horseradish-peroxidase (HRP). Dilute to working concentration of 0.5 μg/mL in detection antibody dilution buffer before use.

Standard: Each vial contains 100 ng of recombinant DLL1. Reconstitute standard powder with 1 mL detection antibody dilution buffer. After reconstitution, store at -20 °C to -80 °C in a manual defrost freezer. A seven-point standard curve using 2-fold serial dilutions in sample dilution buffer, and a high standard of 3000 pg/mL is recommended.

Sensitivity: The minimum detectable dose of Human DLL1 was determined to be approximately 46.875 pg/mL. This is defined as at least three times standard deviations above the mean optical density of 10 replicates of the zero standard.
Components
  • Capture Ab
  • Detection Ab
  • Standard
Material not included CBS - 0.05 M
Na2CO3 - 0.05 M
NaHCO3, pH 9.6, 0.2 μm filtered
TBS - 25 mM
Tris, adjust pH to 7.4 by HCl
Wash Buffer - 0.05 % Tween20 in TBS, pH 7.2 - 7.4
Blocking Buffer - 5 % BSA in Wash Buffer
Sample dilution buffer - 0.5 % BSA in wash buffer, pH 7.2 - 7.4, 0.2 μm filtered
Detection antibody dilution buffer - 0.5 % BSA in wash buffer, pH 7.2 - 7.4, 0.2 μm filtered
Substrate Solution: To achieve best assay results, fresh substrate solution is recommended Substrate stock solution - 10 mg/mL TMB (Tetramethylbenzidine ) in DMSO Substrate dilution buffer - 0.05 M Na2HPO4 and 0.025 M citric acid , adjust pH to 5.5
Substrate working solution - For each plate dilute 250 μL substrate stock solution in 25 mL substrate dilutionbuffer and then add 80 μL 0.75 % H2O2 , mix it well
Stop Solution - 2 N H2SO4
Alternative Name DLL1
Background Delta-like protein 1, also known as Drosophila Delta homolog 1, H-Delta-1, and DLL1, is a single-pass typeI membrane protein which contains one DSL domain and eight EGF-like domains. DLL1 is expressed in heart andpancreas, with lower expression in brain and muscle and almost no expression in placenta, lung, liver and kidney. DLL1acts as a ligand for Notch receptors. DLL1 blocks the differentiation of progenitor cells into the B-cell lineage whilepromoting the emergence of a population of cells with the characteristics of a T-cell/NK-cell precursor. The Notchpathway is an evolutionary conserved intercellular signaling pathway involved in numerous biological processesincluding cell fate determination, cellular differentiation, proliferation, survival, and apoptosis. In mammalian cells, fiveNotch ligands (Jagged1, 2, DLL1, DLL3, DLL4) and four Notch receptors (Notch 1-4) have been identified, and ligand-receptor interactions results in proteolysis and translocation of the Notch intracellular domain. Analysis of DLL1 mutantsreveals that it is necessary and sufficient to maintain a pool of progenitors in the embryonic neuroepithelium. DLL1serves to prevent the untimely differentiation of neural progenitors. DLL1 also contributes to the control of proliferationand differentiation in (Interfollicular Epidermis) IFE.
Research Area Embryogenesis, Embryonic stem cells, Hematopoietic Progenitors, Hematopoietic Stem Cells, Transcription Factors, Neurogenesis, Lineage Markers
Application Notes Optimal working dilution should be determined by the investigator.
Protocol This ELISA Pair Set is a solid phase sandwich ELISA (Enzyme-Linked Immunosorbent Assay). It utilizes a monoclonal antibody specific for DLL1 coated on a 96-well plate. Standards and samples are added to the wells, and any DLL1 present binds to the immobilized antibody. The wells are washed and a horseradish peroxidase conjugated mouse anti-DLL1 monoclonal antibody is then added, producing an antibody-antigen-antibody "sandwich". The wells are again washed and TMB substrate solution is loaded, which produces color in proportion to the amount of DLL1 present in the sample. To end the enzyme reaction, the stop solution is added and absorbances of the microwell are read at 450 nm.
Reagent Preparation
  1. Dilute the capture antibody to the working concentration in CBS. Immediately coat a 96-well microplate with 100 μL per well of the diluted capture antibody. Seal the plate and incubate overnight at 4 °C.
    2. Aspirate each well and wash with at least 300 μL wash buffer, repeating the process two times for a total of three washes. Complete removal of liquid at each step is essential for good performance. After the last wash, remove any remaining wash buffer by inverting the plate and blotting it against clean paper towels.
    3. Block plates by adding 300 μL of blocking buffer to each well. Incubate at room temperature for a minimum of 1 hour.
    4. Repeat the aspiration/wash as in step 2. The plates are now ready for sample addition.
Assay Procedure
  1. Add 100 μL of sample or standards in sample dilution buffer per well. Seal the plate and incubate 2 hours at roomtemperature.
    2. Repeat the aspiration/wash as in step 2 of plate preparation.
    3. Add 100 μL of the detection antibody, diluted in antibody dilution buffer, to each well. Seal the plate and incubate 1hour at room temperature.
    4. Repeat the aspiration/wash as in step 2 of plate preparation.
    5. Add 200 μL of substrate solution to each well. Incubate for 20 minutes at room temperature (if substrate solutionis not as requested, the incubation time should be optimized). Avoid placing the plate in direct light.
    6. Add 50 μL of stop solution to each well. Gently tap the plate to ensure thorough mixing.
    7. Determine the optical density of each well immediately, using a microplate reader set to 450 nm.
Calculation of Results

Calculate the mean absorbance for each set of duplicate standards, controls and samples. Subtract the mean zero standard absorbance from each. Construct a standard curve by plotting the mean absorbance for each standard on the y-axis against the concentration on the x-axis and draw a best fit curve through the points on the graph. To determine the concentration of the unknowns, find the unknowns' mean absorbance value on the y-axis and draw a horizontal line to the standard curve. At the point of intersection, draw a vertical line to the x-axis and read the concentration. If samples have been diluted, the concentration read from the standard curve must be multiplied by the dilution factor. Alternatively, computer-based curve-fitting statistical software may also be employed to calculate the concentration of the sample.

Restrictions For Research Use only
Format Liquid
Handling Advice Avoid repeated freeze-thaw cycles.
Storage -20 °C,-80 °C
Storage Comment Capture Antibody: Aliquot and store at -20°C to -80°C for up to 6 months from date of receipt. Avoid repeated freeze-thaw cycles.

Detection Antibody: Protect it from prolonged exposure to light. Aliquot and store at -20°C to -80°C and for up to 6 months from date of receipt. Avoid repeated freeze-thaw cycles.

Standard: Store lyophilized standard at -20°C to -80°C for up to 6 months from date of receipt. Aliquot and store the reconstituted Standard at -80°C for up to 1 month. Avoid repeated freeze-thaw cycles.
Expiry Date 6 months
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