Human Cytokine Array G7

Produktnummer ABIN625589

Produktdetails

Reaktivität: Human

Nachweismethode: Fluorometric

Methodentyp: Sandwich ELISA

Applikation: Antibody Array (AA)

Verwendungszweck: G-Series Human Cytokine Antibody Array 7 Kit. Detects 60 Human Cytokines. Suitable for all liquid sample types.

Marke: RayBio®

Proben: Serum, Plasma, Cell Culture Supernatant, Cell Lysate, Tissue Lysate

Analytische Methode: Semi-Quantitative

Spezifität: Adiponectin (ACRP30), AgRP, Angiopoietin-2, Amphiregulin, Axl, bFGF, beta-NGF, Betacellulin (BTC), CCL28 (MEC), CTACK (CCL27), Dtk, EGFR, ENA-78 (CXCL5), Fas (TNFRSF6/Apo-1), FGF-4, FGF-9, GCSF, GITR Ligand (TNFSF18), GITR (TNFRSF18), GRO alpha/beta/gamma, GRO alpha (CXCL1), HCC-4 (CCL16), HGF, ICAM-1 (CD54), ICAM-3 (CD50), IGFBP-3, IGFBP-6, IGF-1 R, IL-1 R4 (ST2), IL-1 R1, IL-11, IL-12 p40, IL-12 p70, IL-17A, IL-2 R alpha, IL-6 R, IL-8 (CXCL8), I-TAC (CXCL11), Lymphotactin (XCL1), MIF, MIP-1 alpha (CCL3), MIP-1 beta (CCL4), MIP-3 beta (CCL19), MSP alpha/beta, NT-4, Osteoprotegerin (TNFRSF11B), Oncostatin M, PLGF, gp130, TNF RII (TNFRSF1B), TNF RI (TNFRSF1A), TECK (CCL25), TIMP-1, TIMP-2, Thrombopoietin (TPO), TRAIL R3 (TNFRSF10C), TRAIL R4 (TNFRSF10D), uPAR, VEGF-A, VEGF-D

Produktmerkmale:

• High sensitivity and specificity
• Low sample volume (10-100 μL per array)
• Large dynamic range of detection
• Compatible with most sample types
• Test 4 or 8 samples on each slide
• Suitable for high-throughput assays

Bestandteile: Cytokine Antibody Array glass slide (4 or 8 arrays per slide)
Biotinylated Detection Antibodies
Streptavidin-conjugated HiLytePlus™ 555 Fluor
Blocking Buffer
20X Wash Buffer I
20X Wash Buffer II
2X Cell Lysis Buffer
G-Series Antibody Array accessories
Accessories include: 16-well incubation chamber with gasket, protective cover, snap-on sides, adhesive film

Benötigtes Material: Small plastic boxes or containers
Pipettors, pipette tips and other common lab consumables
Orbital shaker or oscillating rocker
Aluminum foil
Gene microarray scanner or similar laser fluorescence scanner

Anwendungsinformationen

Applikationshinweise: Completely cover array area with sample or buffer during incubation. Avoid foaming during incubation steps. Perform all incubation and wash steps under gentle rocking or rotation. Cover the incubation chamber with adhesive film during incubation, particularly when incubation is more than 2 hours or <70 μL of sample or reagent is used. Several incubation steps such as step 6 (blocking), step 7 (sample incubation), step 10 (detection antibody incubation), or step 13 (Cy3 equivalent dyestreptavidin incubation) may be done overnight at 4 °C. Please make sure to cover the incubation chamber tightly to prevent evaporation.

Kommentare:

The G-Series arrays feature fluorescent signal detection. The antibodies are spotted on glass slide solid supports and require a laser scanner for data collection.
All G-Series arrays work on the sandwich ELISA principle, utilizing a matched pair of antibodies: an immobilized capture antibody and a corresponding biotinylated detection antibody.

Probenmenge: 100 μL

Testdauer: 6 h

Plattentyp: Glass Slide

Protokoll:

1. Dry the glass slide
2. Block array surface
3. Incubate with Sample
4. Incubate with Biotinylated Detection Antibody Cocktail
5. Incubate with Streptavidin-Conjugated Fluor
6. Disassemble the glass slide
7. Scan with a gene microarray laser scanner
8. Perform densitometry and analysis

Aufbereitung der Proben:

Use serum-free conditioned media if possible. If serum-containing conditioned media is required, it is highly recommended that complete medium be used as a control since many types of sera contains cytokines. We recommend the following parameters for your samples: 50 to 100 µl of original or diluted serum, plasma, cell culture media, or other body fluid, or 50-500 µg/ml of protein for cell and tissue lysates. If you experience high background or if the fluorescent signal intensities exceed the detection range, further dilution of your sample is recommended.

Testdurchführung:

Take out the glass slide from the box, and let it equilibrate to room temperature inside the sealed plastic bag for 20-30 minutes. Remove slide from the plastic bag, peel off the cover film, and let it air dry for another 1-2 hours.

Blocking & Incubation
1. Add 100 µl Sample Diluent into each well and incubate at room temperature for 30 minutes to block slides.
2. Decant buffer from each well. Add 100 µl of sample to each well. Incubate arrays at room temperature for 1-2 hour.
3. Decant the samples from each well, and wash 5 times (5 min each) with 150 µl of 1X Wash Buffer I at room temperature with gentle shaking. Completely remove wash buffer in each wash step. Dilute 20x Wash Buffer I with H2O.
4. Decant the 1x Wash Buffer I from each well, wash 2 times (5 min each) with 150 µl of 1X Wash Buffer II at room temperature with gentle shaking.Completely remove wash buffer in each wash step. Dilute 20X Wash Buffer II with H2O.

Incubation with Biotinylated Antibody Cocktail & Wash
5. Reconstitute the detection antibody by adding 1.4 ml of Sample Diluent to the tube. Spin briefly.
6. Add 80 µl of the detection antibody cocktail to each well. Incubate at room temperature for 1-2 hour.
7. Decant the samples from each well, and wash 5 times (5 mins each) with 150 µl of 1X Wash Buffer I and then 2 times with 150 µl of 1x Wash Buffer II at room temperature with gentle shaking. Completely remove wash buffer in each wash step.

Incubation with Cy3 Equivalent Dye-Streptavidin & Wash
8. After briefly spinning down, add 1.4 ml of Sample Diluent to Cy3 equivalent dye-conjugated streptavidin tube. Mix gently.
9. Add 80 µl of Cy3 equivalent dye-conjugated streptavidin to each well. Cover the device with aluminum foil to avoid exposure to light or incubate in dark room. Incubate at room temperature for 1 hour.
10. Decant the samples from each well, and wash 5 times (5 mins each) with 150 µl of 1X Wash Buffer I at room temperature with gentle shaking. Completely remove wash buffer in each wash step.

Fluorescence Detection
11. Disassemble the device by pushing clips outward from the slide side. Carefully remove the slide from the gasket.
12. Place the slide in the Slide Washer/Dryer (a 4-slide holder/centrifuge tube), add enough 1x Wash Buffer I (about 30 ml) to cover the whole slide, and then gently shake at room temperature for 15 minutes. Decant Wash Buffer I. Wash with 1x Wash Buffer II (about 30 ml) and gently shake at room temperature for 5 minutes.
13. Remove water droplets completely by gently applying suction with a pipette to remove water droplets. Do not touch the array, only the sides.
14. Imaging: The signals can be visualized through use of a laser scanner equipped with a Cy3 wavelength (green channel) such as Axon GenePix.

Ergebnisberechnung:

Data extraction can be done using the GAL file that is specific for this array along with the microarray analysis software (GenePix, ScanArray Express, ArrayVision, MicroVigene, etc.).

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Handhabung: Do not touch the surface of the slides, as the microarray slides are very sensitive. Hold the slides by the edges only. Handle all buffers and slides with powder free gloves. Handle glass slide/s in clean environment. The G-Series slides do not have bar codes. To help distinguish one slide from another, transcribe the slide serial number from the slide bag to the back of the slide with a fine point permanent marker. Please write the number on the very bottom edge of the slide, taking care to avoid writing on the array well areas.

Lagerung: -20 °C

Informationen zur Lagerung: For best results, store the entire kit frozen at -20°C upon arrival. Stored frozen, the kit will be stable for at least 6 months which is the duration of the product warranty period. Once thawed, store array slide(s) and 1X Blocking Buffer at -20°C and all other reagents undiluted at 4°C for no more than 3 months.

Haltbarkeit: 6 months

Referenzen

Shi, Zhang, Zhou, Xin, Jiang, Jiang, Wu, Li, Ding, Li, Sun, Li, Zhou, Zhang, Jin, Hao, Chen, Cao, Li, Li, Chen, Li: "Quantitative evaluation of human bone mesenchymal stem cells rescuing fulminant hepatic failure in pigs." in: Gut, Vol. 66, Issue 5, pp. 955-964, (2017) (PubMed).

Yu, Okawa, Okita, Kamano, Wang, Saeki, Yatani, Egusa: "Gingival Fibroblasts as Autologous Feeders for Induced Pluripotent Stem Cells." in: Journal of dental research, Vol. 95, Issue 1, pp. 110-8, (2016) (PubMed).

Wu, Ding, Han, Arriens, Wei, Han, Pedroza, Jiang, Anolik, Petri, Sanz, Saxena, Mohan: "Antibody-Array-Based Proteomic Screening of Serum Markers in Systemic Lupus Erythematosus: A Discovery Study." in: Journal of proteome research, Vol. 15, Issue 7, pp. 2102-14, (2016) (PubMed).

Wolf, Siegert, Rothmiller, Scheithauer, Strobelt, Steinritz, Worek, Thiermann, Schmidt: "Characterization of sulfur mustard resistant keratinocyte cell line HaCaT/SM." in: Toxicology letters, Vol. 244, pp. 49-55, (2016) (PubMed).

Matte, Lane, Laplante, Garde-Granger, Rancourt, Piché: "Ovarian cancer ascites enhance the migration of patient-derived peritoneal mesothelial cells via cMet pathway through HGF-dependent and -independent mechanisms." in: International journal of cancer. Journal international du cancer, Vol. 137, Issue 2, pp. 289-98, (2015) (PubMed).

Xin, Ding, Hao, Jiang, Zhou, Wu, Shi, Cao, Li, Li: "Human bone marrow mesenchymal stem cell-derived hepatocytes express tissue inhibitor of metalloproteinases 4 and follistatin." in: Liver international : official journal of the International Association for the Study of the Liver, (2015) (PubMed).

Bermudez, Sendon-Lago, Eiro, Treviño, Gonzalez, Yebra-Pimentel, Giraldez, Macia, Lamelas, Saa, Vizoso, Perez-Fernandez: "Corneal epithelial wound healing and bactericidal effect of conditioned medium from human uterine cervical stem cells." in: Investigative ophthalmology & visual science, Vol. 56, Issue 2, pp. 983-92, (2015) (PubMed).

Matsubara, Matsushita, Sakai, Kano, Kondo, Noda, Hashimoto, Imagama, Ishiguro, Suzumura, Ueda, Furukawa, Yamamoto: "Secreted ectodomain of sialic acid-binding Ig-like lectin-9 and monocyte chemoattractant protein-1 promote recovery after rat spinal cord injury by altering macrophage polarity." in: The Journal of neuroscience : the official journal of the Society for Neuroscience, Vol. 35, Issue 6, pp. 2452-64, (2015) (PubMed).

Kostallari, Baba-Amer, Alonso-Martin, Ngoh, Relaix, Lafuste, Gherardi: "Pericytes in the myovascular niche promote post-natal myofiber growth and satellite cell quiescence." in: Development (Cambridge, England), Vol. 142, Issue 7, pp. 1242-53, (2015) (PubMed).

Zhu, Tang, Gang, Wang, Wang, Lei, Feng, Fang, Yan: "Antibody microarray profiling of osteosarcoma cell serum for identifying potential biomarkers." in: Molecular medicine reports, Vol. 12, Issue 1, pp. 1157-62, (2015) (PubMed).

Schwartzbaum, Seweryn, Holloman, Harris, Handelman, Rempala, Huang, Burkholder, Brandemihl, Kallberg, Johannesen, Ahlbom, Feychting, Grimsrud: "Association between Prediagnostic Allergy-Related Serum Cytokines and Glioma." in: PLoS ONE, Vol. 10, Issue 9, pp. e0137503, (2015) (PubMed).

Gomez, ODriscoll, Sheets, Hruban, Oberholzer, McGarrigle, Shamblott: "Neurogenin 3 Expressing Cells in the Human Exocrine Pancreas Have the Capacity for Endocrine Cell Fate." in: PLoS ONE, Vol. 10, Issue 8, pp. e0133862, (2015) (PubMed).

Vanarsa, Ye, Han, Xie, Mohan, Wu: "Inflammation associated anemia and ferritin as disease markers in SLE." in: Arthritis research & therapy, Vol. 14, Issue 4, pp. R182, (2014) (PubMed).

Yang, Li, Li, Li, Li, Kong, Liu, Wang, Lv: "MCP-1 stimulates MMP-9 expression via ERK 1/2 and p38 MAPK signaling pathways in human aortic smooth muscle cells." in: Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology, Vol. 34, Issue 2, pp. 266-76, (2014) (PubMed).

Brunt, Wu, Chen, Poeckel, Dercho, Melo, Funk, Ward, Li: "Ex vivo Akt/HO-1 gene therapy to human endothelial progenitor cells enhances myocardial infarction recovery." in: Cell transplantation, Vol. 21, Issue 7, pp. 1443-61, (2013) (PubMed).

Mahlknecht, Stemberger, Sprenger, Rainer, Hametner, Kirchmair, Grabmer, Scherfler, Wenning, Seppi, Poewe, Reindl: "An antibody microarray analysis of serum cytokines in neurodegenerative Parkinsonian syndromes." in: Proteome science, Vol. 10, Issue 1, pp. 71, (2013) (PubMed).

Matsushita, Toiyama, Tanaka, Saigusa, Hiro, Uchida, Inoue, Kusunoki: "Soluble CXCL16 in preoperative serum is a novel prognostic marker and predicts recurrence of liver metastases in colorectal cancer patients." in: Annals of surgical oncology, Vol. 19 Suppl 3, pp. S518-27, (2012) (PubMed).

Liu, Teoh, Chong, Lee, Mattar, Randhawa, Zhang, Medina, Kamm, Fisk, Choolani, Chan: "Vasculogenic and osteogenesis-enhancing potential of human umbilical cord blood endothelial colony-forming cells." in: Stem cells (Dayton, Ohio), Vol. 30, Issue 9, pp. 1911-24, (2012) (PubMed).

Straussman, Morikawa, Shee, Barzily-Rokni, Qian, Du, Davis, Mongare, Gould, Frederick, Cooper, Chapman, Solit, Ribas, Lo, Flaherty, Ogino, Wargo, Golub: "Tumour micro-environment elicits innate resistance to RAF inhibitors through HGF secretion." in: Nature, Vol. 487, Issue 7408, pp. 500-4, (2012) (PubMed).

Greulich, Maxhera, Vandenplas, de Wiza, Smiris, Mueller, Heinrichs, Blumensatt, Cuvelier, Akhyari, Ruige, Ouwens, Eckel: "Secretory products from epicardial adipose tissue of patients with type 2 diabetes mellitus induce cardiomyocyte dysfunction." in: Circulation, Vol. 126, Issue 19, pp. 2324-34, (2012) (PubMed).

Antigendetails

Hintergrund: Cytokines play an important role in innate immunity, apoptosis, angiogenesis, cell growth and differentiation. They are involved in interactions between different cell types, cellular responses to environmental conditions, and maintenance of homeostasis. In addition, cytokines are also involved in most disease processes, including cancer and cardiac diseases.