Human IL-8/CXCL8 Quantikine HS ELISA Kit Summary
| Background |
The Quantikine HS Human IL-8 Immunoassay is a 4.5 hour solid phase ELISA designed to measure IL-8 levels in serum and plasma. It contains E. coli-expressed recombinant human IL-8 and antibodies raised against the recombinant factor. This immunoassay has been shown to quantitate recombinant human IL-8 accurately. Results obtained using natural human IL-8 showed linear curves that were paralle...l to the standard curves obtained using the Quantikine HS kit standards. These results indicate that this kit can be used to determine relative mass values for natural human IL-8. |
| Specificity |
Natural and recombinant human IL-8
|
| Source |
N/A |
| Assay Type |
Solid Phase Sandwich ELISA |
| Inter-Assay |
|
| Intra-Assay |
|
| Spike Recovery |
|
| Sample Volume |
|
| Gene |
CXCL8 |
Applications/Dilutions
| Dilutions |
|
| Application Notes |
No significant interference observed with available related molecules. |
| Publications |
|
Packaging, Storage & Formulations
| Storage |
Store the unopened product at 2 - 8 °C. Do not use past expiration date. |
Notes
This product is produced by and ships from R&D Systems, Inc., a Bio-Techne brand.
Alternate Names for Human IL-8/CXCL8 Quantikine HS ELISA Kit
Background
Interleukin-8 (IL-8), also known as IL-8, GCP-1, and NAP-1,
is a heparin-binding 8-9 kDa member of the alpha, or CXC family of chemokines.
There are at least 15 human CXC family members that all adopt a three
beta -sheet/one alpha -helix structure. Most CXC chemokines show an N-terminal
Glu-Leu-Arg (ELR) tripeptide motif. IL-8 circulates as a monomer, homodimer,
and heterodimer with CXCL4/PF4. The monomer is considered the most bio-active,
while the heterodimer can potentiate PF4 activity. IL-8 oligomerization is
modulated by its interactions with matrix and cell surface glycosaminoglycans
(GAGs). Mature human IL-8 shares 65-69% amino acid (aa) identity with canine,
feline, and porcine IL-8. There is no IL-8 gene counterpart in rodent.
Multiple isoforms of IL-8 are generated through both
alternative splicing and differential proteolytic cleavage. In humans,
alternative splicing generates an iso-form with an eleven aa substitution at
the C-terminus. Proteolytic processing results in N-terminal truncation of IL-8
and is likely a cell-specific event. For example, fibroblasts and endothelial
cells generate the 1-77 form by cleaving IL-8 following Glu21, while monocytes
and lymphocytes generate the 6-77 form by cleaving following Leu25. These
truncated forms generally show increased bioactivity, particularly through the
CXCR1 receptor. IL-8 can also undergo citrullination on Arg27 of the precursor,
a modification that increases its half-life and ability to induce leukocytosis.
A wide variety of cells secrete IL-8 including monocytes and neutrophils, fibroblasts
and keratinocytes, mast cells, visceral smooth muscle cells, dendritic cells,
type II great alveolar cells, and endothelial cells.
IL-8 bioactivity is mediated through two G-protein-coupled
receptors, termed CXCR1/IL-8 RA and CXCR2/IL-8 RB. CXCR1 is 45-50 kDa in size
and is used almost exclusively by IL-8. CXCR2 is 35-40 kDa in size and is used
by nearly all CXC chemokines. Both CXCR1 and CXCR2 constitutively associate
into functional homodimers. They can also heterodimerize, but these complexes
dissociate following IL-8 binding. CXCR2 responds to low concentrations of IL-8
and is principally associated with chemotaxis and MMP-9 release. CXCR1, in
contrast, responds to high concentrations of IL-8 and is associated with
respiratory burst and phospholipase D2 activation. Thus, CXCR2 ligation induces
leukocyte adhesion to activated vascular endothelium and migration to sites of
inflammation, while CXCR1 ligation primes neutrophil antimicrobial activity.
IL-8 can also form a complex with Serpin A1/alpha-1 Antitrypsin, and this
prevents IL-8 interaction with CXCR1.
In addition to its pro-inflammatory effects, IL-8 is
involved in angiogenesis and the pathogenesis of atherosclerosis and cancer. It
induces VEGF expression in vascular endothelial cells and functions as an
autocrine factor for EC growth and angiogenesis. It is upregulated in
atherosclerotic lesions and is elevated in the serum and cerebrospinal fluid
following myocardial infarction. In cancer, IL-8 promotes
epithelial-mesenchymal transition as well as tumor cell invasiveness and
metastasis.
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Product General Protocols
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FAQs for CXCL8/IL-8 (HS800). (Showing 1 - 1 of 1 FAQs).
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What is the difference between the Quantikine and Duoset ELISA kits?
- Our Quantikine kits are fully optimized and validated for the sample types listed on the product specific webpage and datasheet, as this can vary between kits. Each kit is supplied ready to use with one pre-coated 96-well plate, a detection antibody directly conjugated to HRP, and all other necessary reagents. These kits are ideal for researchers who want the convenience of a ready to use and optimized ELISA product. Some of these kits are also available prepackaged in larger 6 and 50 plate sizes.Our DuoSet Kits, in contrast, are ELISA development kits containing the capture and detection antibody, the mass-value calibrated standard, and streptavidin-HRP to prepare approximately 5 or 15 plates. Ancillary reagents will need to be used/purchased, and for most kits, we will recommend one of our Ancillary Reagent Kits, which contain the reagents we use ourselves in-house. DuoSet kits are validated only for cell culture supernatant samples and therefore require further development and validation for accurate measurement in more complex samples such as serum and plasma. Our DuoSet Kits offer an economical, flexible alternative for the experienced ELISA user.