CXCL1 Kit ELISA

N° du produit ABIN625445

Détail du produit CXCL1 Kit ELISA

Antigène: CXCL1 (Chemokine (C-X-C Motif) Ligand 1 (Melanoma Growth Stimulating Activity, Alpha) (CXCL1))

Reactivité: Rat

Méthode de détection: Colorimetric

Type de méthode: Sandwich ELISA

Gamme de detection: 300-15000 pg/mL

Seuil minimal de détection: 300 pg/mL

Application: ELISA

Fonction: Rat CINC-1 (CXCL1) ELISA Kit for cell culture supernatants, Heparin and/or EDTA treated plasma, and serum samples. Citrate is not recommended.

Type d'échantillon: Plasma, Cell Culture Supernatant, Serum

Analytical Method: Quantitative

Specificité: This ELISA kit shows no cross-reactivity with any of the cytokines tested: rat CINC-2, CINC-3, CNTF, IL-1 alpha, IL-1 beta, IL-6, IL-10, GM-CSF, IFN-gamma, Leptin, Lix, MCP-1, MIP-3 alpha, beta-NGF, TIMP-1, TNF-alpha, VEGF.

Sensibilité: < 300 pg/mL

Attributs du produit:

• Strip plates and additional reagents allow for use in multiple experiments
• Quantitative protein detection
• Establishes normal range
• The best products for confirmation of antibody array data

Ingrédients:

• Pre-Coated 96-well Strip Microplate
• Wash Buffer
• Stop Solution
• Assay Diluent(s)
• Lyophilized Standard
• Biotinylated Detection Antibody
• Streptavidin-Conjugated HRP
• TMB One-Step Substrate

Matériel non inclus:

• Distilled or deionized water
• Precision pipettes to deliver 2 μL to 1 μL volumes
• Adjustable 1-25 μL pipettes for reagent preparation
• 100 μL and 1 liter graduated cylinders
• Tubes to prepare standard and sample dilutions
• Absorbent paper
• Microplate reader capable of measuring absorbance at 450nm
• Log-log graph paper or computer and software for ELISA data analysis

Information d'application

Indications d'application: Recommended Dilution for serum and plasma samples2 fold

Volume d'échantillon: 100 μL

Plaque: Pre-coated

Protocole:

1. Prepare all reagents, samples and standards as instructed in the manual.
2. Add 100 μL of standard or sample to each well.
3. Incubate 2.5 h at RT or O/N at 4 °C.
4. Add 100 μL of prepared biotin antibody to each well.
5. Incubate 1 h at RT.
6. Add 100 μL of prepared Streptavidin solution to each well.
7. Incubate 45 min at RT.
8. Add 100 μL of TMB One-Step Substrate Reagent to each well.
9. Incubate 30 min at RT.
10. Add 50 μL of Stop Solution to each well.
11. Read at 450 nm immediately.

Préparation des réactifs:

1. Bring all reagents and samples to room temperature (18 - 25 °C) before use.
   2. Sample dilution: 1x Assay Diluent D (Item K) should be used for dilution of serum/plasma samples. 1x Assay Diluent B should be used for dilution of cell culture supernates. Suggested dilution for normal serum/plasma: 2 fold. Please note that levels of the target protein may vary between different specimens. Optimal dilution factors for each sample must be determined by the investigator.
   3. Assay Diluent B and Assay Diluent D should be diluted 5-fold with deionized or distilled water before use.
   4. Preparation of standard: Briefly spin the vial of Item C and then add 500 µL 1x Assay Diluent D (for serum/plasma samples) or 1x Assay Diluent B (for cell culture supernates) into Item C vial to prepare a 50 ng/mL standard. Dissolve the powder thoroughly by a gentle mix. Add 150 µL CINC-1 standard (50 ng/mL) from the vial of Item C, into a tube with 350 µL 1x Assay Diluent D to prepare a 15,000 pg/mL standard solution. Pipette 250 µL 1x Assay Diluent D into each tube. Use the 15,000 pg/mL standard solution to produce a dilution series . Mix each tube thoroughly before the next transfer. 1x Assay Diluent D serves as the zero standard (0 pg/mL). The 15,000 pg/mL standard in Assay Diluent B is saturated, we recommend to start from 3,000 pg/mL for Assay Diluent B standard curve. 1x Assay Diluent B serves as the zero standard (0 pg/mL). 250 µL 250 µL 250 µL 250 µL 250 µL 150 µL standard (15 ng/mL) + 350 µL 250myl 15,000 7,500 3,750 1,875 937.5 468.8 234.4 0 pg/mL pg/mL pg/mL pg/mL pg/mL pg/mL pg/mL pg/mL
   5. If the Wash Concentrate (20x) (Item B) contains visible crystals, warm to room temperature and mix gently until dissolved. Dilute 20 ml of Wash Buffer Concentrate into deionized or distilled water to yield 400 ml of 1x Wash Buffer.
   6. Briefly spin the Detection Antibody vial (Item F) before use. Add 100 µL of 1x Assay Diluent B into the vial to prepare a detection antibody concentrate. Pipette up and down to mix gently (the concentrate can be stored at 4 °C for 5 days). The detection antibody concentrate should be diluted 80-fold with 1x Assay Diluent B and used in step 4 of Part VI Assay Procedure.
   7. Briefly spin the HRP-Streptavidin concentrate vial (Item G) and pipette up and down to mix gently before use. HRP-Streptavidin concentrate should be diluted 200-fold with 1x Assay Diluent B. For example: Briefly spin the vial (Item G) and pipette up and down to mix gently . Add 50 µL of HRP-Streptavidin concentrate into a tube with 10 ml 1x Assay Diluent B to prepare a 200-fold diluted HRP-Streptavidin solution (don't store the diluted solution for next day use). Mix well.

Procédure de l'essai:

1. Bring all reagents and samples to room temperature (18 - 25 °C) before use. It is recommended that all standards and samples be run at least in duplicate.
   2. Add 100 µL of each standard (see Reagent Preparation step 2) and sample into appropriate wells. Cover well and incubate for 2.5 hours at room temperature or over night at 4 °C with gentle shaking.
   3. Discard the solution and wash 4 times with 1x Wash Solution. Wash by filling each well with Wash Buffer (300 myl) using a multi-channel Pipette or autowasher. Complete removal of liquid at each step is essential to good performance. After the last wash, remove any remaining Wash Buffer by aspirating or decanting. Invert the plate and blot it against clean paper towels.
   4. Add 100 µL of 1x prepared biotinylated antibody (Reagent Preparation step 6) to each well. Incubate for 1 hour at room temperature with gentle shaking.
   5. Discard the solution. Repeat the wash as in step
   6. Add 100 µL of prepared Streptavidin solution (see Reagent Preparation step 7) to each well. Incubate for 45 minutes at room temperature with gentle shaking.
   7. Discard the solution. Repeat the wash as in step
   8. Add 100 µL of TMB One-Step Substrate Reagent (Item H) to each well. Incubate for 30 minutes at room temperature in the dark with gentle shaking.
   9. Add 50 µL of Stop Solution (Item I) to each well. Read at 450 nm immediately.

Calcul des résultats:

Calculate the mean absorbance for each set of duplicate standards, controls and samples, and subtract the average zero standard optical density. Plot the standard curve on log-log graph paper or using Sigma plot software, with standard concentration on the x-axis and absorbance on the y-axis. Draw the best-fit straight line through the standard points.
Typical Data: These standard curves are for demonstration only. A standard curve must be run with each assay. Assay Diluent D Rat CINC-1 concentration (pg/mL) O D =4 50 n m 0.001 0.01 0.1 1 10 100 1,000 10,000 100,00 Assay Diluent B Rat CINC-1 concentration (pg/mL) O D =4 50 n m 0.01 0.1 1 10 10 100 1,000 10,000
Sensitivity: The minimum detectable dose of CINC-1 is typically less than 300 pg/mL in Assay Diluent D and 50 pg/mL in Assay Diluent B.
Recovery: Recovery was determined by spiking various levels of rat CINC-1 into rat serum, plasma (EDTA and heparin) and cell culture media. Mean recoveries are as follows: Sample Type Average % Recovery Range ( %) Serum 99.64 88-107 Plasma 107.9 97-125 Cell culture media 112.5 99-122
Linearity: Sample Type Serum Plasma Cell Culture Media (EDTA and heparin) 1:2 Average % of Expected 98.67 99.97 82.27 Range ( %) 88-106 90-109 74-90 1:4 Average % of Expected 125.1 89.14 75.54 Range ( %) 116-133 70-120 67-82
Reproducibility: Intra-Assay: CV<10 % Inter-Assay: CV<12 %

Précision du teste: Intra-Assay: CV< 10 % Inter-Assay: CV< 12 %

Restrictions: For Research Use only

Stockage

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

Stock: -20 °C

Stockage commentaire: The entire kit may be stored at -20°C for up to 1 year from the date of shipment. Avoid repeated freeze-thaw cycles. The kit may be stored at 4°C for up to 6 months. For extended storage, it is recommended to store at -80°C.

Date de péremption: 6 months

Références pour CXCL1 Kit ELISA (ABIN625445)

Li, Liu, Sun, Wang, Wang, Wang, Wang: "Chronic vagus nerve stimulation attenuates vascular endothelial impairments and reduces the inflammatory profile via inhibition of the NF-κB signaling pathway in ovariectomized rats." dans: Experimental gerontology, Vol. 74, pp. 43-55, (2016) (PubMed).

Détail du antigène

Antigène: CXCL1 (Chemokine (C-X-C Motif) Ligand 1 (Melanoma Growth Stimulating Activity, Alpha) (CXCL1))

Autre désignation: CINC-1 (CXCL1 Produits)

Synonymes: FSP Kit ELISA, GRO1 Kit ELISA, GROa Kit ELISA, MGSA Kit ELISA, MGSA-a Kit ELISA, NAP-3 Kit ELISA, SCYB1 Kit ELISA, CINC-1 Kit ELISA, Gro1 Kit ELISA, CXCL1 Kit ELISA, Sdf1 Kit ELISA, Fsp Kit ELISA, KC Kit ELISA, Mgsa Kit ELISA, N51 Kit ELISA, Scyb1 Kit ELISA, gro Kit ELISA, GRO Kit ELISA, Gro Kit ELISA, C-X-C motif chemokine ligand 1 Kit ELISA, chemokine (C-X-C motif) ligand 1 (melanoma growth stimulating activity, alpha) Kit ELISA, C-X-C motif chemokine ligand 12 Kit ELISA, chemokine (C-X-C motif) ligand 1 Kit ELISA, CXCL1 Kit ELISA, Cxcl1 Kit ELISA, Cxcl12 Kit ELISA, GRO1 Kit ELISA

Sujet: Growth-regulated alpha protein (C-X-C motif chemokine 1) (Cytokine-induced neutrophil chemoattractant 1) (CINC-1) (Platelet-derived growth factor-inducible protein KC)

ID gène: 81503

UniProt: P14095

Pathways: Autophagy