ELISA Kit for the Quantitative Analysis of Human CXCL16

The human CXCL16 ELISA (enzyme-linked immunosorbent assay) kit is used for detection of human CXCL16 in cell culture supernatants,human serum and plasma.THE ELISA KIT IS FOR RESEARCH USE ONLY.Please read this instruction manual carefully and check out the material provided before use, and you can contact with our company if any questions. You can enter our website or call us for other aim.

Introduction

CXC chemokine ligand 16 (CXCL16)，a member of the chemokine superfamily，is a type I membrane protein containing a non­ELRmotif­containing CXC chemokine domain , a mucin-like spacer region, a transmembrane domain and a cytoplasmic domain with consensus tyrosine phosphorylation and SH2 binding sites. The gene for human CXCL16 predicts a 254 amino acid (aa) protein with an N-terminal signal peptide of 27 aa.Human and mouseCXCL16 share70% aa sequence similarity within their chemokine domains.

CXCL16 has been detected in various human organs except for brain, bone marrow, skeletal muscle or colon.It plays a putative role in directing leukocyte migration and functioning as a scavenger receptor. In plasma cells, CXCL16 can stimulate chemotactic migration and enhances adhesion to fibronectin.Myeloma cells also adhere to immobilized CXCL16 in a manner dependent upon CXCR6,which is identified asthe receptor of CXCL16. In addition, CXCL16 mediates the uptake of phosphatidylserine and oxidized low density lipoprotein (Ox-LDL), and the phagocytosis by APCs of both gram-negative and gram-positive bacteria.

Principles of the Test

The kit is a solid sandwich enzyme-linked immunosorbent assay for detection of human CXCL16. An anti-human CXCL16 monoclonal antibody has been absorbed onto the wells of the microtiter strips provided. Samples including specimens or standards were pipetted into wells. The human CXCL16 in specimens or standards would be captured by the coated antibody and the free others were removed by washing. The human CXCL16 biotin-conjugated antibody were added and binds to human CXCL16 captured by the first antibody, which formed a sandwich. Streptavidin-HRP would be added and binds to the biotin conjugated antibody, then free Streptavidin-HRP would be removed during a wash step. After this, substrate solution would be added and catalyzed by the HRP, and a coloured product is formed. The intensity of the colored product is used to calculate in proportion to the amount of human CXCL16 in the original specimen.

Materials provided with the kit:

Reagent	96/48Test Kit
Assay Buffer	5ml/3 ml
Human CXCL16 Antibody-Coated Wells	12 strips/6 strips
5X Standard Diluent	10ml/5ml
Human CXCL16 Standard	2/1vial(s)
Human CXCL16Detection Antibody	10ml/5ml
Streptavidin-HRP	10ml/5ml
Wash Buffer Concentrate 20×	30ml/15ml
TMB	10ml/5ml
Stop Solution	5ml/3 ml
Plate Covers	3/2
Complete Instruction Manual	1

Specimen Collection

1.Collecting specimen as following:

A.The particulate of the cell culture supernatants should be removed before use.

B.Serum was obtained from clot at room temperature.

C.Please collect plasma with EDTA.

D.Assay immediately or store samples at -20℃. Avoid free-thaw cycles.

2.Antiseptic and anticoagulant should not appear in Serum

samples.

3.Any particulate should be removed from samples before use.

4. Do not use grossly hemolyzed or lipemic samples.

Note: Strongly recommend that the serum and plasma samples should be diluent as doubling dilution before use.

Precautions for use:

1.Please storage the Kit at 2～8℃。

2. Washing buffer concentrate may have crystal in low temperature, and you can melt its in water-bath before use.

3. Please discard theremains after useof the dissolved standard.

4.Avoid contact of substrate solution with oxidizing agents and metal.

5.Usage of disposable pipette tips avoid microbial contamination or cross-contamination of reagents or specimens.

6. Do not mix or substitute reagents with those from other lots or other sources.

7. To ensure the adequate mixture of added reagents, please tap gently the plate after the wells were filled with liquid.

8. Incubation temperature should be 25～28℃.

9. Wash step was crucial for whole assay process.

10. Duplicate wells of the same sample were recommended in

assay process.

11. Avoid the foam while pour the liquid into wells.

12. For serum or plasma samples ,the biotin-conjugated antibody should be incubate for at least 90 minutes.

Reagent Preparation

1.The reagents should be warmed up to room temperature before use.The remanent reagents must reseal and put into refrigeratory again as soon as possible.

2.Dilute 1.5ml of wash buffer Concentrate into 19ml deionized or distilled water to work.

3. If you have a 5x standard diluent, please dilute it with double steaming water or deionized water.

4. Add standard diluent to the bottle according to the volume of the label and wait15 minutes for complete dissolution. Incubation temperature should be 25～28℃。And in turn add the half concentration diluent by standard diluent

Wash step:

Automated microplate washer or operating by pipette: Each well should be pour into300ul wash buffer and soak 15 or 30 seconds,then be aspirated, five times process were repeated. After the last wash, remove remaining wash buffer by aspirating.Invert the plate and blot it against clean paper towels.

Materials Required But Not Provided

1. pipettes and pipette tips

2. Microwell strip reader capable of reading at 450 nm (540 nm asoptional reference wave length)

3. automated microplate washer

4.Glass-distilled or deionized water

Assay procedure

1.The needed strips were putted into the frame, the remains were returned into foil pouch and resealed.

2.Blank well were recommended, which only color reagent and stop solution be added. It is suggested that each testing with gradient density of standard for standard curve.

3.Add 100ul of standard or sample.Cover with the Plate Covers provided.Incubate for 2 hours at room temperatureIf assay the serum sample,you should add 50μl assay buffer with 50μl sample into the wells,if the protein concentration is higher than the range of the Kit, add the same quantitys assay buffer with the sample, the deficiency should be complemented with sample diluent to 100μl per well.

4.Five times wash process were repeated.

5.Add 100ul of detection antibody. Cover with the Plate Covers provided.Incubate for 1 hour at room temperature.

6.Five times wash process were repeated.

7.Add 100ul of Streptavidin-HRP. Cover with the Plate Covers provided. Lucifugal incubation for 20 minutes at room temperature.

8.Five times wash process were repeated.

9.Add 100ul of TMB，Lucifugal incubation for 20 minutes at room temperature.

10.Add 50ul of stop solution to each well, determine the opticaldensity of each well within 10 minutes.

Calculation of Results

1.Duplicates should be within 20 percent of the mean. Average absorbance values for each set of duplicate samples were used as detection results.

2.The blank absorbance values of subtract should be deducted.

3.Drawing a best fit curve through the points of graph. Draw the standard curve by plotting assayed OD value (on the Y axis) vs. concentration (on the X axis). The sample concentration was obtained based on its OD value founding in the standard concentration curve.

4.If the values obtained are not within the expected range of the standard, Samples should be dilute and assay again

TypicalData and Standard Curve

Human CXCL16 Standard Curve

 

Sensitivity,Specificity, Repeatability

Sensitivity: repeated assays were evaluated and the minimum detectable dose was 12.4pg/ml.

Specificity: No significant cross-reactivity or interference with human BLC/BCA-1, Fractalkine, CTACK, GROb and mouse 6Ckine,CXCL16.

Repeatability: The coefficient of variation between wells or plates is less than 10 per cent.