CD36 Kit ELISA

N° du produit ABIN1889439

Détail du produit CD36 Kit ELISA

Antigène: CD36

Épitope: AA 30-439

Reactivité: Rat

Méthode de détection: Colorimetric

Type de méthode: Sandwich ELISA

Gamme de detection: 218-14.000 pg/mL

Seuil minimal de détection: 218 pg/mL

Application: ELISA

Fonction: Sandwich High Sensitivity ELISA kit for Quantitative Detection of Rat CD36/SR-B3

Marque: PicoKine™

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

Analytical Method: Quantitative

Specificité: Expression system for standard: CHO
Immunogen sequence: G30-K439

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

Sensibilité: <10pg/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: CHO
Immunogen sequence: G30-K439

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.

Commentaires:

Tissue Specificity: Expressed at high levels in heart, intestine, spleen, adipose tissue, skeletal muscle and, at lower levels, in testes. .

Plaque: Pre-coated

Protocole: rat CD36 ELISA Kit was based on standard sandwich enzyme-linked immune-sorbent assay technology. A monoclonal antibody from mouse specific for CD36 has been precoated onto 96-well plates. Standards(CHO, G30-K439) and test samples are added to the wells, a biotinylated detection polyclonal antibody from goat specific for CD36 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 rat CD36 amount of sample captured in plate.

Procédure de l'essai:

Aliquot 0.1 mL per well of the 14,000pg/mL, 7,000pg/mL, 3500pg/mL, 1750pg/mL, 875pg/mL, 437pg/mL, 218pg/mL rat CD36 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 rat cell culture supernates, serum or plasma(heparin, EDTA) to each empty well. See "Sample Dilution Guideline" above for details. It is recommended that each rat CD36 standard solution and each sample be measured in duplicate.

Précision du teste:

• Sample 1: n=16, Mean(ng/ml): 1.97, Standard deviation: 0.075, CV(%): 3.8
• Sample 2: n=16, Mean(ng/ml): 5.32, Standard deviation: 0.282, CV(%): 5.3
• Sample 3: n=16, Mean(ng/ml): 7.88, Standard deviation: 0.362, CV(%): 4.6,
• Sample 1: n=24, Mean(ng/ml): 2.35, Standard deviation: 0.101, CV(%): 4.3
• Sample 2: n=24, Mean(ng/ml): 5.92, Standard deviation: 0.378, CV(%): 6.4
• Sample 3: n=24, Mean(ng/ml): 8.04, Standard deviation: 0.442, CV(%): 5.5

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

Détail du antigène

Antigène: CD36

Autre désignation: CD36 (CD36 Produits)

Synonymes: BDPLT10 Kit ELISA, CHDS7 Kit ELISA, FAT Kit ELISA, GP3B Kit ELISA, GP4 Kit ELISA, GPIV Kit ELISA, PASIV Kit ELISA, SCARB3 Kit ELISA, Fat Kit ELISA, Scarb3 Kit ELISA, GPIIIB Kit ELISA, PAS-4 Kit ELISA, zgc:92513 Kit ELISA, CD36 molecule Kit ELISA, CD36 molecule (thrombospondin receptor) Kit ELISA, CD36 Kit ELISA, Cd36 Kit ELISA, cd36 Kit ELISA

Sujet:

Protein Function: Binds to collagen, thrombospondin, anionic phospholipids and oxidized low-density lipoprotein (oxLDL). May function as a cell adhesion molecule. Directly mediates cytoadherence of Plasmodium falciparum parasitized erythrocytes. Binds long chain fatty acids and may function in the transport and/or as a regulator of fatty acid transport (By similarity). Receptor for thombospondins, THBS1 AND THBS2, mediating their antiangiogenic effects (By similarity). As a coreceptor for TLR4-TLR6, promotes inflammation in monocytes/macrophages. Upon ligand binding, such as oxLDL or amyloid-beta 42 binding, rapidly induces the formation of a heterodimer of TLR4 and TLR6, which is internalized and triggers inflammatory signals, leading to the NF-kappa-B-dependent production of CXCL1, CXCL2 and CCL9 cytokines, via MYD88 signaling pathway, and CCL5 cytokine, via TICAM1 signaling pathway, as well as IL1B secretion. .

Background: CD36 (Cluster of Differentiation 36) is an integral membrane protein found on the surface of many cell types in vertebrate animals and is also known as FAT, SCARB3, GP88, glycoprotein IV (gpIV) and glycoprotein IIIb (gpIIIb). The human CD36 is a member of a gene family of structurally related glycoproteins and functions as a receptor for collagen type I and thrombospondin. The use of a CD36 genomic probe has allowed the localization of the CD36 locus to the 7q11.2 band by fluorescence in situ hybridization coupled with GTG-banding. CED-1/SCARF1 and C03F11.3/CD36 are beta-glucan binding receptors and define an evolutionarily conserved pathway for the innate sensing of fungal pathogens.

Synonyms: Platelet glycoprotein 4,Adipocyte membrane protein,Fatty acid translocase,Fatty acid transport protein,Glycoprotein IIIb,GPIIIB,PAS IV,PAS-4,Platelet glycoprotein IV,GPIV,CD36,Cd36,Fat,

Full Gene Name: Platelet glycoprotein 4

Cellular Localisation: Cell membrane, Multi-pass membrane protein. Upon ligand-binding, internalized through dynamin-dependent endocytosis..

ID gène: 29184

UniProt: Q07969

Pathways: Signalisation TLR, Peptide Hormone Metabolism, Response to Growth Hormone Stimulus, Activation of Innate immune Response, Cellular Response to Molecule of Bacterial Origin, Regulation of Lipid Metabolism by PPARalpha, Positive Regulation of Immune Effector Process, Production of Molecular Mediator of Immune Response, Hepatitis C, Toll-Like Receptors Cascades, Lipid Metabolism, S100 Proteins