CXCL5 ELISA Kit
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- Target See all CXCL5 ELISA Kits
- CXCL5 (Chemokine (C-X-C Motif) Ligand 5 (CXCL5))
- Binding Specificity
- AA 37-114
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Reactivity
- Human
- Detection Method
- Colorimetric
- Method Type
- Sandwich ELISA
- Detection Range
- 31.2-2000 pg/mL
- Minimum Detection Limit
- 31.2 pg/mL
- Application
- ELISA
- Purpose
- Sandwich High Sensitivity ELISA kit for Quantitative Detection of Human CXCL5/ENA-78
- Brand
- PicoKine™
- Sample Type
- Cell Culture Supernatant, Serum, Plasma (heparin), Plasma (EDTA), Plasma (citrate)
- Analytical Method
- Quantitative
- Specificity
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Expression system for standard: E.coli
Immunogen sequence: A37-N114 - Cross-Reactivity (Details)
- There is no detectable cross-reactivity with other relevant proteins.
- Sensitivity
- <10pg/mL
- Material not included
- Microplate reader in standard size. Automated plate washer. Adjustable pipettes and pipette tips. Multichannel pipettes are recommended in the condition of large amount of samples in the detection. Clean tubes and Eppendorf tubes. Washing buffer (neutral PBS or TBS). Preparation of 0.01M TBS: Add 1.2g Tris, 8.5g Nacl
- Immunogen
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Expression system for standard: E.coli
Immunogen sequence: A37-N114 - Featured
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- Application Notes
- Before using Kit, spin tubes and bring down all components to bottom of tube. Duplicate well assay was recommended for both standard and sample testing.
- Comment
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Sequence similarities: Belongs to the intercrine alpha (chemokine CxC) family.
- Plate
- Pre-coated
- Protocol
- human CXCL5 ELISA Kit was based on standard sandwich enzyme-linked immune-sorbent assay technology. A monoclonal antibody from mouse specific for CXCL5 has been precoated onto 96-well plates. Standards(E.coli, A37-N114) and test samples are added to the wells, a biotinylated detection polyclonal antibody from goat specific for CXCL5 is added subsequently and then followed by washing with PBS or TBS buffer. Avidin-Biotin-Peroxidase Complex was added and unbound conjugates were washed away with PBS or TBS buffer. HRP substrate TMB was used to visualize HRP enzymatic reaction. TMB was catalyzed by HRP to produce a blue color product that changed into yellow after adding acidic stop solution. The density of yellow is proportional to the human CXCL5 amount of sample captured in plate.
- Assay Procedure
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Aliquot 0.1 mL per well of the 2000pg/mL,1000pg/mL, 500pg/mL, 250pg/mL, 125pg/mL, 62.5pg/mL, 31.2pg/mL human CXCL5 standard solutions into the precoated 96-well plate. Add 0.1 mL of the sample diluent buffer into the control well (Zero well). Add 0.1 mL of each properly diluted sample of human cell culture supernates, serum or plasma(heparin, EDTA, citrate) to each empty well. See "Sample Dilution Guideline" above for details. It is recommended that each human CXCL5 standard solution and each sample be measured in duplicate.
- Assay Precision
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- Sample 1: n=16, Mean(pg/ml): 214, Standard deviation: 18.19, CV(%): 8.5
- Sample 2: n=16, Mean(pg/ml): 448, Standard deviation: 26.4, CV(%): 5.9
- Sample 3: n=16, Mean(pg/ml): 1094, Standard deviation: 50.32, CV(%): 4.6,
- Sample 1: n=24, Mean(pg/ml): 209, Standard deviation: 18.39, CV(%): 8.8
- Sample 2: n=24, Mean(pg/ml): 442, Standard deviation: 34.9, CV(%): 7.9
- Sample 3: n=24, Mean(pg/ml): 1021, Standard deviation: 72.49, CV(%): 7.1
- Restrictions
- For Research Use only
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- Handling Advice
- Avoid multiple freeze-thaw cycles.
- Storage
- -20 °C,4 °C
- Storage Comment
- Store at 4°C for 6 months, at -20°C for 12 months. Avoid multiple freeze-thaw cycles
- Expiry Date
- 12 months
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CXCL5 as an autocrine or paracrine cytokine is associated with proliferation and migration of hepatoblastoma HepG2 cells." in: Oncology letters, Vol. 14, Issue 6, pp. 7977-7985, (2017) (PubMed).
: "
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CXCL5 as an autocrine or paracrine cytokine is associated with proliferation and migration of hepatoblastoma HepG2 cells." in: Oncology letters, Vol. 14, Issue 6, pp. 7977-7985, (2017) (PubMed).
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- Target See all CXCL5 ELISA Kits
- CXCL5 (Chemokine (C-X-C Motif) Ligand 5 (CXCL5))
- Alternative Name
- CXCL5 (CXCL5 Products)
- Synonyms
- ENA-78 ELISA Kit, SCYB5 ELISA Kit, Cxcl6 ELISA Kit, CXCL5 ELISA Kit, GCP-2 ELISA Kit, GCP2 ELISA Kit, SCYB6 ELISA Kit, AMCF-II ELISA Kit, LIX ELISA Kit, Scyb5 ELISA Kit, Scyb6 ELISA Kit, C-X-C motif chemokine ligand 5 ELISA Kit, C-X-C motif chemokine ligand 6 ELISA Kit, chemokine (C-X-C motif) ligand 5 ELISA Kit, C-X-C motif chemokine 5 ELISA Kit, CXCL5 ELISA Kit, Cxcl6 ELISA Kit, LOC701946 ELISA Kit, LOC703222 ELISA Kit, Cxcl5 ELISA Kit
- Background
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Protein Function: Involved in neutrophil activation. In vitro, ENA-78(8- 78) and ENA-78(9-78) show a threefold higher chemotactic activity for neutrophil granulocytes. .
Background: C-X-C motif chemokine 5 is a protein that in humans encoded by the CXCL5 gene. The protein encoded by this gene, CXCL5 is a small cytokine belonging to the CXC chemokine family that is also known as epithelial-derived neutrophil-activating peptide 78(ENA-78). It is produced following stimulation of cells with the inflammatory cytokines interleukin-1or tumor necrosis factor-alpha. Expression of CXCL5 has also been observed in eosinophils, and can be inhibited with the type II interferon IFN-gamma. This chemokine stimulates the chemotaxis of neutrophils possessing angiogenic properties. It elicits these effects by interacting with the cell surface chemokine receptor CXCR2. The gene for CXCL5 is encoded on four exons and is located on humanchromosome 4 amongst several other CXC chemokine genes. CXCL5 has been implicated in connective tissue remodeling. CXCL5 plays a role in reducing sensitivity to sunburn pain in some subjects, and is a potential target which can be utilized to understand more about pain in other inflammatory conditions like arthritis and cystitis.
Synonyms: C-X-C motif chemokine 5,ENA-78(1-78),Epithelial-derived neutrophil-activating protein 78,Neutrophil-activating peptide ENA-78,Small-inducible cytokine B5,ENA-78(8-78),ENA-78(9-78),CXCL5,ENA78, SCYB5,
Full Gene Name: C-X-C motif chemokine 5
Cellular Localisation: Secreted. - Gene ID
- 6374
- UniProt
- P42830
- Pathways
- Cellular Response to Molecule of Bacterial Origin, Regulation of Leukocyte Mediated Immunity
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