Nori Ferret IgG ELISA Kit

Price range: $508.00 through $916.00

Datasheet   

This ELISA kit is for quantification of IgG in ferret. 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 IgG has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and any IgG present is bound by the immobilized antibody. After washing away any unbound substances, a detection antibody specific for IgG 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 IgG bound in the initial step. The color development is stopped, and the intensity of the color is measured.

Alternative names for IgG: Immunoglobulin G

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

CAT: GR201141 Categories: , Tags: ,

Description

Nori Ferret IgG ELISA Kit Summary

Alternative names for IgG: Immunoglobulin G

Alternative names for Black-footed ferret, European domestic ferret

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 na
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 300 pg/mL
Detection Range 1.563-100 ng/mL
Specificity Ferret IgG
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:

Immunoglobulin G (IgG) is antibody molecule. Each IgG is composed of four peptide chains — two heavy chains γ and two light chains. IgG antibodies are large molecules of about 150 kDa composed of four peptide chains. It contains two identical class γ heavy chains of about 50 kDa and two identical light chains of about 25 kDa, thus a tetrameric quaternary structure. The two heavy chains are linked to each other and to a light chain each by disulfide bonds. The resulting tetramer has two identical halves, which together form the Y-like shape. Each end of the fork contains an identical antigen binding site. The Fc regions of IgGs bear a highly conserved N-glycosylation site. The N-glycans attached to this site are predominantly core-fucosylated diantennary structures of the complex type. In addition, small amounts of these N-glycans also bear bisecting GlcNAc and α-2, 6-linked sialic acid residues (1). IgG antibodies are involved in predominantly the secondary immune response. The presence of specific IgG, in general, corresponds to maturation of the antibody response (2). IgG can bind to many kinds of pathogens, for example viruses, bacteria, and fungi, and protects the body against them by agglutination and immobilization, complement activation (classical pathway), opsonization for phagocytosis, and neutralization of their toxins.

References

  1. Stadlmann J, et al. (2008). Proteomics 8 (14): 2858.
  2. Azeredo da Silveira S, et al. (2002). J Exp Med. 195(6): 665–72.

 

 

Product Citations

  1. Alam RTM et al. (2020) Heamonchus Contortus infection in sheep and goats: alterations in haematological, biochemical, immunological, trace element and oxidative stress markers. J Applied Animal Res doi:org/10.1080/09712119.220. Impact factor: 1.248. Products used and cited: Nori Sheep IgG, IgE and IgM ELISA Kits.
  2. Wlazlo L et al. (2021) Effects of fermented rapseed meal on the gastrointestinal microbiota and immune status of rabbit. Animals 11:716. Impact factor: 2.62. Products used and cited: Nori Rabbit IgA, IgG and IgM ELISA Kits.
  3. Rostami F et al. (2021) Effects of scrophularia striata hydroalcoholic extract in comparison to salinomycin on growth performance, intestinal health and immunity in broiler chickens following a mixed-species Eimeria challenge. Vet Parasitol 293:109417. org/10.1016/j.vetpar.2021.109417. Impact factor: 2.009. Products used and cited: Nori Chicken IgM, IgG, TGFβ1 and IL-6 ELISA Kits.
  4. Wlazlol, et al. (2021) Effect of fermented rapeseed meal on the gastrointestinal microbiota and immune status of rabbit (oryctolagus cuniculus). Animalsorg/10.3390/ani11030716. Impact factor: 1.654. Products used and cited: Nori Rabbit IgA, IgG and IgM ELISA Kits
  5. Migda A et al. (2022) Effectiveness of immunization with multi‑component bacterial immunomodulator in foals at 35th day of life. Nature Portfolio 12:15795. https://doi.org/10.10381/s41598-022-17532-1. Impact factor: 15.7. Products used and cited: Nori Equine IgG2, IgM, IL-6, IL-10 ELISA Kits.
  6. Abdulrahman A Almehizia et al. (2023) Anti‑inflammatory activity of novel derivatives of pyrazolo [3,4d] pyridazine against digestive system inflammation. Nauryn-Schmiedberg’s Archives of Pharmacology https://doi.org/10.1007/s00210.023-02493-7. Impact factor: 3.1. Products used and cited: Nori Mouse IL-22, TNFa, RANKL, IgM, IgG ELISA Kit.
  7. Ahmed Mohammed Darwish et al. (2022) Effectiveness of new selenium‑enriched mutated probiotics in reducing inflammatory effects of piroxicam medication in liver and kidney. Inflammopharmacology 30:2097-2106. Impact factor: 5.3. Products used and cited: Nori Mouse IgG, IgM, IL-22, TNFa ELISA Kit.
  8. Abd EI-Nasser Khattab et al. (2023) Anti‑inflammatory and Immunomodulatory Potency of Selenium‑Enriched Probiotic Mutants in Mice with Induced Ulcerative Colitis. Biological Trace Element Res 201:353-367. Impact factor: 3.8. Products used and cited: Nori Mouse IgG, IgM, IL-2, IL-6, IL-10, TNFa ELISA Kit.

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