CXCL2 Kit ELISA

N° du produit ABIN921067

Détail du produit CXCL2 Kit ELISA

Antigène: CXCL2 (Chemokine (C-X-C Motif) Ligand 2 (CXCL2))

Épitope: AA 28-100

Reactivité: Souris

Méthode de détection: Colorimetric

Type de méthode: Sandwich ELISA

Gamme de detection: 15.6-1000 pg/mL

Seuil minimal de détection: 15.6 pg/mL

Application: ELISA

Fonction: Sandwich High Sensitivity ELISA kit for Quantitative Detection of Mouse MIP-2

Marque: PicoKine™

Type d'échantillon: Cell Culture Supernatant, Serum, Plasma (heparin), Plasma (EDTA)

Analytical Method: Quantitative

Specificité: Expression system for standard: E.coli
Immunogen sequence: A28-N100

Réactivité croisée (Details): There is no detectable cross-reactivity with other relevant proteins.

Sensibilité: <5pg/mL

Matériel non inclus: 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

Immunogène: Expression system for standard: E.coli
Immunogen sequence: A28-N100

Information d'application

Indications d'application: 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.

Plaque: Pre-coated

Protocole: mouse MIP-2 ELISA Kit was based on standard sandwich enzyme-linked immune-sorbent assay technology. A monoclonal antibody from rat specific for MIP-2 has been precoated onto 96-well plates. Standards(E.coli, A28-N100) and test samples are added to the wells, a biotinylated detection polyclonal antibody from goat specific for MIP-2 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 mouse MIP-2 amount of sample captured in plate.

Procédure de l'essai:

Aliquot 0.1 mL per well of the 1000pg/mL, 500pg/mL, 250pg/mL, 125pg/mL, 62.5pg/mL, 31.2pg/mL, 15.6pg/mL mouse MIP-2 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 mouse cell culture supernates, serum or plasma(heparin, EDTA) to each empty well. See "Sample Dilution Guideline" above for details. It is recommended that each mouse MIP-2 standard solution and each sample be measured in duplicate.

Précision du teste:

• Sample 1: n=16, Mean(pg/ml): 113, Standard deviation: 4.41, CV(%): 3.9
• Sample 2: n=16, Mean(pg/ml): 355, Standard deviation: 17.75, CV(%): 5
• Sample 3: n=16, Mean(pg/ml): 627, Standard deviation: 40.13, CV(%): 6.4,
• Sample 1: n=24, Mean(pg/ml): 134, Standard deviation: 8.31, CV(%): 6.2
• Sample 2: n=24, Mean(pg/ml): 387, Standard deviation: 21.3, CV(%): 5.5
• Sample 3: n=24, Mean(pg/ml): 653, Standard deviation: 44.4, CV(%): 6.8

Restrictions: For Research Use only

Stockage

Conseil sur la manipulation: Avoid multiple freeze-thaw cycles.

Stock: -20 °C,4 °C

Stockage commentaire: Store at 4°C for 6 months, at -20°C for 12 months. Avoid multiple freeze-thaw cycles

Date de péremption: 12 months

Références pour CXCL2 Kit ELISA (ABIN921067)

Du, Chen, Wang, Sun: "Pathway analysis of global gene expression change in dendritic cells induced by the polysaccharide from the roots of Actinidia eriantha." dans: Journal of ethnopharmacology, Vol. 214, pp. 141-152, (2018) (PubMed).

Roux, Schaefers, Clark, Weatherholt, Renaud, Scott, LiPuma, Priebe, Gerard, Yoder-Himes: "A putative lateral flagella of the cystic fibrosis pathogen Burkholderia dolosa regulates swimming motility and host cytokine production." dans: PLoS ONE, Vol. 13, Issue 1, pp. e0189810, (2018) (PubMed).

Roux, Weatherholt, Clark, Gadjeva, Renaud, Scott, Skurnik, Priebe, Pier, Gerard, Yoder-Himes: "Immune Recognition of the Epidemic Cystic Fibrosis Pathogen Burkholderia dolosa." dans: Infection and immunity, Vol. 85, Issue 6, (2017) (PubMed).

Détail du antigène

Antigène: CXCL2 (Chemokine (C-X-C Motif) Ligand 2 (CXCL2))

Autre désignation: CXCL2 (CXCL2 Produits)

Synonymes: CINC-2a Kit ELISA, GRO2 Kit ELISA, GROb Kit ELISA, MGSA-b Kit ELISA, MIP-2a Kit ELISA, MIP2 Kit ELISA, MIP2A Kit ELISA, SCYB2 Kit ELISA, GRO3 Kit ELISA, Gro2 Kit ELISA, MIP-2 Kit ELISA, Mgsa-b Kit ELISA, Mip2 Kit ELISA, Scyb Kit ELISA, Scyb2 Kit ELISA, Mip-2 Kit ELISA, GROB Kit ELISA, MIP-2alpha Kit ELISA, C-X-C motif chemokine ligand 2 Kit ELISA, chemokine (C-X-C motif) ligand 2 Kit ELISA, CXCL2 Kit ELISA, Cxcl2 Kit ELISA

Sujet:

Protein Function: Chemotactic for human polymorphonuclear leukocytes but does not induce chemokinesis or an oxidative burst.

Background: MIP is a member of the aquaporin family of membrane-bound water channels. MIP family proteins are thought to contain 6 TM domains. Sequence analysis suggests that the proteins may have arisen through tandem, intragenic duplication from an ancestral protein that contained 3 TM domains. Major intrinsic protein(MIP, also called MP26) is the predominant fiber cell membrane protein of the ocular lens. The major intrinsic protein(MIP) of the vertebrate eye lens is the first identified member of a sequence-related family of cell-membrane proteins that appears to have evolved by gene duplication. Several members of the MIP family transport water(aquaporins), glycerol and other small molecules in microbial, plant and animal cells. The standard used in this kit is recombinant mouse MIP-2(A28-N100), consisting of 73 amino acids with the molecular mass of 8KDa.

Synonyms: C-X-C motif chemokine 2,Macrophage inflammatory protein 2,MIP2,Cxcl2,Mip-2, Mip2, Scyb2,

Full Gene Name: C-X-C motif chemokine 2

Cellular Localisation: Secreted.

ID gène: 20310

UniProt: P10889

Pathways: Cellular Response to Molecule of Bacterial Origin