Human Transferrin / TF ELISA Pair Set

Details zu Produkt Nr. ABIN2010533, Anbieter: Anmelden zum Anzeigen
Antigen
  • PRO1557
  • PRO2086
  • TFQTL1
  • transferrin
  • TF
Reaktivität
Human
Wirt
Maus
Konjugat
HRP
Methodentyp
Sandwich ELISA
Applikation
ELISA
Optionen
Hersteller
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Verwendungszweck The human Transferrin / TF ELISA Pair Set is for the quantitative determination of human Transferrin .
This ELISA Pair Set contains the basic components required for the development of sandwich ELISAs.
Nachweismethode Colorimetric
Sensitivität 15.6 pg/mL
Produktmerkmale Capture Antibody: 0.5 mg/mL of mouse anti-Transferrin / TF monoclonal antibody. Dilute to a working concentration of 2 μg/mL in CBS before coating

Detection Antibody: 0.4 mg/mL mouse anti-Transferrin / TF monoclonal antibody conjugated to horseradish-peroxidase (HRP). Dilute to working concentration of 1 μg/mL in detection antibody dilution buffer before use.

Standard: Each vial contains 70 ng of recombinant Transferrin. Reconstitute 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 usi ng 2-fold serial dilutions in sample dilution buffer, and a high standard of 1 ng/mL is recommended

Sensitivity: The minimum detectable dose of human Transferrin / TF was determined to be approximately 15.6 pg/mL. This is defined as at least three times standard deviations above the mean optical density of 10 replicates of the zero standard
Bestandteile
  • Capture Ab
  • Detection Ab
  • Standard
Benötigtes Material 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
Hintergrund Transferrin, also known as Serotransferrin, Beta-1 metal-binding globulin, TF, is a secreted protein which belongs tothe transferrin family. It is expressed by the liver and secreted in plasma and contains two transferrin-like domains. Transferrins are iron binding transport proteins which can bind two Fe3+ ions in association with the binding of an anion, usually bicarbonate. It is responsible for the transport of iron from sites of absorption and heme degradation to those ofstorage and utilization. Serum transferrin may also have a further role in stimulating cell proliferation. When a transferrinprotein loaded with iron encounters a transferrin receptor on the surface of a cell, it binds to it and, as a consequence, istransported into the cell in a vesicle. Transferrin is a glycoprotein that binds iron very tightly but reversibly. Although ironbound to transferrin is less than 0. 1 % ( 4 mg) of the total body iron, it is the most important iron pool, with the highestrate of turnover ( 25 mg/24 h) . Defects in transferrin are the cause of a transferrinemia (ATRAF) which is rareautosomal recessive disorder characterized by iron overload and hypochromic anemia. Transferrin is also associatedwith the innate immune system.
Applikationshinweise Optimal working dilution should be determined by the investigator.
Protokoll This ELISA Pair Set is a solid phase sandwich ELISA (Enzyme-Linked Immunosorbent Assay). It utilizes a monoclonal antibody specific forTransferrin / TF coated on a 96-well plate. Standards and samples are added tothe wells, and any Transferrin / TF present binds to the immobilized antibody.The wells are washed and a horseradish peroxidase conjugated mouse anti-Transferrin / TF monoclonal antibody is then added, producing anantibody-antigen-antibody "sandwich". The wells are again washed and TMBsubstrate solution is loaded, which produces color in proportion to the amountof Transferrin / TF present in the sample. To end the enzyme reaction, the stopsolution is added and absorbances of the microwell are read at 450 nm.
Aufbereitung der Reagenzien
  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.
Testdurchführung
  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.
Ergebnisberechnung

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.

Beschränkungen Nur für Forschungszwecke einsetzbar
Format Liquid
Handhabung Avoid repeated freeze-thaw cycles.
Lagerung -20 °C,-80 °C
Informationen zur Lagerung 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.
Haltbarkeit 6 months
Bilder des Herstellers
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