Nori Salmon IL-1b ELISA Kit

$461.00$832.00

DataSheet   

This ELISA kit is for quantification of IL-1β in salmon. This is a quick ELISA assay that reduces time to 50% compared to the conventional method, and the entire assay only takes 3 hours. This assay employs the quantitative sandwich enzyme immunoassay technique and uses biotin-streptavidin chemistry to improve the performance of the assays. An antibody specific for IL-1β has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and any IL-1β present is bound by the immobilized antibody. After washing away any unbound substances, a detection antibody specific for IL-1β is added to the wells. Following wash to remove any unbound antibody reagent, a detection reagent is added. After intensive wash a substrate solution is added to the wells and color develops in proportion to the amount of IL-1β bound in the initial step. The color development is stopped, and the intensity of the color is measured.

Alternative names for IL-1b: Interleukin 1 beta, IL1b

This product is for laboratory research use only not for diagnostic and therapeutic purposes or any other purposes.

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Description

Nori Salmon IL-1b ELISA Kit Summary

Alternative names for IL-1b: Interleukin 1 beta, IL1b

 

Assay Type Solid Phase Sandwich ELISA
Format 96-well Microplate or 96-Well Strip Microplate
Method of Detection Colorimetric
Number of Targets Detected 1
Target Antigen Accession Number XP_045549382.1
Assay Length 3 hours
Quantitative/Semiquantitative Quantitative
Sample Type Plasma, Serum, Cell Culture, Urine, Cell/Tissue Lysates, Synovial Fluid, BAL,
Recommended Sample Dilution (Plasma/Serum) No dilution for sample <ULOQ; sufficient dilution for samples >ULOQ
Sensitivity 15 pg/mL
Detection Range 78.13-5000 pg/mL
Specificity Salmon IL-1b
Cross-Reactivity < 0.5% cross-reactivity observed with available related molecules, < 50% cross-species reactivity observed with species tested.
Interference No significant interference observed with available related molecules
Storage/Stability 4 ºC for up to 6 months
Usage For Laboratory Research Use Only. Not for diagnostic or therapeutic use.
Additional Notes The kit allows for use in multiple experiments.

 

Standard Curve

 

Kit Components
1. Pre-coated 96-well Microplate
2. Biotinylated Detection Antibody
3. Streptavidin-HRP Conjugate
4. Lyophilized Standards
5. TMB One-Step Substrate
6. Stop Solution
7. 20 x PBS
8. Assay Buffer

Other Materials Required but not Provided:
1. Microplate Reader capable of measuring absorption at 450 nm
2. Log-log graph paper or computer and software for ELISA data analysis
3. Precision pipettes (1-1000 µl)
4. Multi-channel pipettes (300 µl)
5. Distilled or deionized water

Protocol Outline
1. Prepare all reagents, samples and standards as instructed in the datasheet.
2. Add 100 µl of Standard or samples to each well and incubate 1 h at RT.
3. Add 100 µl of Working Detection Antibody to each well and incubate 1 h at RT.
4. Add 100 µl of Working Streptavidin-HRP to each well and incubate 20 min at RT.
5. Add 100 µl of Substrate to each well and incubate 5-30 min at RT.
6. Add 50 µl of Stop Solution to each well and read at 450 nm immediately.

Background: 

Interleukin-1 beta (IL-1β) also known as catabolin, is a member of the interleukin 1 cytokine family.  IL-1β precursor is cleaved by caspase 1 (interleukin 1 beta convertase). Cytosolic thiol protease cleaves the product to form mature IL-1β.  Interleukin-1 alpha and interleukin-1 beta forms IL-1 (1,2,3). IL-1β is produced by activated macrophages as a proprotein, which is proteolytically processed to its active form by caspase 1 (CASP1/ICE). This cytokine is an important mediator of the inflammatory response, and is involved in a variety of cellular activities, including cell proliferation, differentiation, and apoptosis. The induction of cyclooxygenase-2 (PTGS2/COX2) by this cytokine in the central nervous system (CNS) is found to contribute to inflammatory pain hypersensitivity. IL-1β gene and eight other interleukin 1 family genes form a cytokine gene cluster on chromosome 2(4).

References

  1. Auron PE, et al (1984). Proc Natl Acad Sci U S A 81 (24): 7907–11.
  2. March CJ, et al. (1985). Nature 315 (6021): 641–7.
  3. Clark BD, et al (1986). Nucleic Acids Res 14 (20): 7897–1914.

 

 

Product Citation

3.        El-Ashker M et al. (2013) Traumatic reticuloperitonitis in https://new.genorise.com/wp-content/uploads/2022/06/Genorise-Product-citation-3.pdfwater buffalo (Bubalus bubalis): clinical finding and the
associated inflammatory response. J Internal Med ID:808656, 1-6.
Product used and cited: GSI Bovine IL-10 ELISA kit      Article
6.        Norton J. et al. (2013) Effect of clenbuterol on tracheal mucociliary transport in horses undergoing simulated long-
distance transportation. J. Vet Intern Med 27(6): 1523-7.
Product used and cited: GSI Equine IL-2, IL-10, TNFα ELISA kits
8.        Marycz K et al. (2014) The activity of IL-6 and TNF-α in adipose tissue and peripheral blood in horses suffering
from equine metabolic syndrome (EMS). Kafkas Univ Vet Fak Dert 20(4):493-499.
Product used and cited: GSI equine IL-6/TNF-α ELISA kits.
11.        El-Atahker et al. (2014) The use of inflammatory marker as a prognostic aid for traumatic reticuloperitonitis in
water buffalo (Bubalus bubalis). Veterinarni Medicina 59(5):239-246.
Product used and cited: GSI Bovine IL-10 ELISA kit.
12.        Vetvick V, Oliveira C (2014) β (1,3) (1-6)-D-Glucan with strong effects on immune status in chicken: potential
importance for efficiency of commercial farming. J. Nutr Health Sci 1(3):1-6.
Product used and cited: GSI Chicken IL-2 ELISA kit.
13.        Razavi SM (2014) Malignant ovine theileriosis: serum concentrations of some inflammatory components and
adenosine deaminase activity. Comparative Clinical Pathology
Product used and cited: GSI Sheep IL-1β ELISA Kit
14.        El-Ashker M et al. (2015) Vitamin C ameliorates gentamicin-induced acute kidney injury in equines: an
experimental study. J. Equine Vet Sci. 35:1-6
Products used and cited: GSI equine IL-β, IL-6, IL-10 and IFN ELISA kits.
15.        Basinska K et al. (2015) The production and distribution of IL-6 and TNF-α in subcutaneous adipose tissue and
their correlation with serum concentrations in Welsh ponies with equine metabolic syndrome. J Vet Sci 16(1):113-120.
Products used and cited: GSI Equine IL-6 and TNF-α ELISA kits
16.        Azma F et al. (2015) A study on the status of inflammatory systems in camels naturally infected with
Toxoplasma gondii. Tropical Animal Health and Production
Products used and cited: GSI Bovine IL-1β ELISA kits
17.        Sandersen C et al. (2015) Effect of inhaled hydrosoluble curcumin on inflammatory markers in broncho-
alveolar lavage fluid of horses with LPS-induced lung neutrophilia. Multisciplinary Respiratory Medicine. 10:16.
Products used and cited: GSI Equine IL-1β/IL-6 ELISA kits
20.        El-Ashker M et al. (2014) Gentamicin-induced acute kidney injury in equines is associated with marked acute phase
response: an experimental study on donkey (Equus asinus). J Vet Sci Med Diagn 4:2.
Products used and cited: equine IL-1β, IL-6, IFN-, IL-10, SAA, haptoglobin, CRP and SA ELISA kits.

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