KEY FEATURES
| Full Name | Chemokine C-X-C-Motif Ligand 16 |
|---|---|
| Synonym | SCYB16, SR-PSOX, CXCLG16 |
| Assay Type | Sandwich |
| Reactivity | Mouse |
| Range | 0.16-10ng/mL |
| Sensitivity | 0.07ng/mL |
| Sample Type | Serum, plasma and other biological fluids |
| Sample Volume | 100μL |
| Detection Wavelength | OD450 |
| Transportation Temperature | 2-8°C |
| Specificity | The kit detected Mouse CXCL16 in the samples and no significant cross-species reactions were found |
| Microplate | 96-wells plate breakable into 12 x 8 wells strip |
TEST PRINCIPLE
| This ELISA kit uses the Sandwich-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with an antibody specific to Mouse CXCL16. Standards or samples are added to the micro ELISA plate wells and combined with the specific antibody. Then a biotinylated detection antibody specific for Mouse CXCL16 and Avidin-Horseradish Peroxidase (HRP) conjugate are added successively to each micro plate well and incubated. Free components are washed away. The substrate solution is added to each well. Only those wells that contain Mouse CXCL16, biotinylated detection antibody and Avidin-HRP conjugate will appear blue in color. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The OD value is proportional to the concentration of Mouse CXCL16. You can calculate the concentration of Mouse CXCL16 in the samples by comparing the OD of the samples to the standard curve. |
ELISA KIT COMPONENTS
Upon receipt, unpack promptly and store as recommended in the instructions.
| Components | Specifications | Storage and Notes |
|---|---|---|
| Micro Plate | 96T: 8 wells×12 strips 48T: 8 wells×6 strips | Unopened: -20°C, 12 months Unused: Put it back in the aluminum foil bag and seal it, store it at -20°C. |
| Reference Standard | 96T: 2 vials 48T: 1 vial | Unopened: -20°C, 12 months Please use freshly dissolved standards for each experiment. Discard any unused standards after dissolution. |
| Biotinylated Detection Ab Concentrate (100×) | 96T: 120μL×1 vial 48T: 60μL×1 vial | Unopened: -20°C, 12 months Unused: Please seal the concentrate and store it at -20°C, and discard the working solution. |
| HRP Conjugate Concentrate (100×) | 96T: 120μL×1 vial 48T: 60μL×1 vial | Unopened: -20°C(Protect from light), 12 months Unused: Please seal the concentrate and store it at -20°C, and discard the working solution. |
| Biotinylated Detection Ab Diluent | 14mL×1 | 2-8℃, 12 months |
| HRP Conjugate Diluent | 14mL×1 | 2-8℃, 12 months |
| Reference Standard & Sample Diluent | 20mL×1 | 2-8℃, 12 months |
| Washing Buffer Concentrate (25×) | 30mL×1 | 2-8℃, 12 months |
| Substrate Reagent(TMB) | 10mL×1 | 2-8°C(Protect from light),12 months |
| Stop Solution | 7mL×1 | 2-8°C/Room temperature |
ASSAY PROCEDURES

TYPICAL DATA

Mouse CXCL16 ELISA Standard Curve
Typical data are for reference only and curves should be replotted for each experiment. The Logistics function is recommended for fitting.
PRECISION
Intra-Assay Precision (Precision within an assay): Three samples of known concentration were tested twenty times on one plate to assess intra-assay precision.
Inter-Assay Precision (Precision between assays): Three samples of known concentration were tested in twenty separate assays to assess inter-assay precision. Assays were performed by at least three technicians using two lots of components.
| Intra-assay Precision | Inter-assay Precision | |||||
|---|---|---|---|---|---|---|
| Sample | 1 | 2 | 3 | 1 | 2 | 3 |
| n | 20 | 20 | 20 | 20 | 20 | 20 |
| Mean (ng/mL) | 0.46 | 1.22 | 4.18 | 0.43 | 1.12 | 3.86 |
| Standard deviation | 0.03 | 0.06 | 0.16 | 0.03 | 0.05 | 0.17 |
| CV(%) | 5.68 | 5.29 | 3.75 | 5.92 | 4.32 | 4.47 |
RECOVERY
The recovery of Mouse CXCL16 spiked to three different levels in samples throughout the range of the assay in various matrices was evaluated.
| Sample Type | Range (%) | Average Recovery (%) |
|---|---|---|
| Serum(n=8) | 86-98 | 92 |
| EDTA plasma (n=8) | 94-107 | 101 |
| Cell culture media (n=8) | 90-102 | 95 |
LINEARITY
To assess the linearity of the assay, samples containing and/or spiked with high concentrations of Mouse CXCL16 in various matrices were diluted with the Reference Standard & Sample Diluent to produce samples with values within the dynamic range of the assay.

Pathways associated with ELISA Kit
| Chemokine Receptors Bind Chemokines Pathway | Chemokine Receptors Bind Chemokines Pathway |
| Chemokine Signaling Pathway | Chemokine Signaling Pathway |
| Class A/1 (Rhodopsin-like Receptors) Pathway | Class A/1 (Rhodopsin-like Receptors) Pathway |
| Cytokine-cytokine Receptor Interaction Pathway | Cytokine-cytokine Receptor Interaction Pathway |
| Defective ACTH Causes Obesity And Pro-opiomelanocortinin Deficiency (POMCD) Pathway | Defective ACTH Causes Obesity And Pro-opiomelanocortinin Deficiency (POMCD) Pathway |
| Disease Pathway | Disease Pathway |
| G Alpha (i) Signalling Events Pathway | G Alpha (i) Signalling Events Pathway |
Diseases associated with MIP-2 ELISA Kit
| Inflammation | publications with MIP-2 and Inflammation |
| Necrosis | publications with MIP-2 and Necrosis |
| Lung Diseases | publications with MIP-2 and Lung Diseases |
| Disease Models, Animal | publications with MIP-2 and Disease Models, Animal |
| Lung Injury | publications with MIP-2 and Lung Injury |
| Pneumonia | publications with MIP-2 and Pneumonia |
| Reperfusion Injury | publications with MIP-2 and Reperfusion Injury |
| Wounds and Injuries | publications with MIP-2 and Wounds and Injuries |
| Edema | publications with MIP-2 and Edema |
| Skin Diseases | publications with MIP-2 and Skin Diseases |
Organs/Tissues associated with MIP-2 ELISA Kit
| Bone Marrow | publications with MIP-2 and Bone Marrow |
| Skin | publications with MIP-2 and Skin |
| Spleen | publications with MIP-2 and Spleen |
| Pancreas | publications with MIP-2 and Pancreas |
| Mammary Gland | publications with MIP-2 and Mammary Gland |
| Vagina | publications with MIP-2 and Vagina |
| Uncharacterized Tissue | publications with MIP-2 and Uncharacterized Tissue |