Product nameCytokine Array – Human Cytokine Antibody Array (Membrane, 60 targets)
See all Cytokine Antibody Array antibody arrays
Sample typeCell culture supernatant, Saliva, Milk, Urine, Serum, Plasma, Cell culture extracts, Other biological fluids, Whole Blood, Tissue Extracts, Cell Lysate, Cell culture media
Species reactivityReacts with: Human
ab169817 is for the simultaneous detection of 60 Human Cytokines. Suitable for all sample types.
Targets: Angiogenin, BDNF, BLC, BMP-4, BMP-6, CK beta 8-1, CNTF, EGF, Eotaxin-1, Eotaxin-2, Eotaxin-3, FGF-6, FGF-7, Flt-3 Ligand, Fractalkine, GCP-2, GDNF, GM-CSF, I-309, IFN-gamma, IGFBP-1, IGFBP-2, IGFBP-4, IGF-1, IL-10, IL-13, IL-15, IL-16, IL-1 alpha, IL-1 beta, IL-1 ra, IL-2, IL-3, IL-4, IL-5, IL-6, IL-7, Leptin, Light, MCP-1, MCP-2, MCP-3, MCP-4, M-CSF, MDC, MIG, MIP-1 delta, MIP-3 alpha, NAP-2, NT-3, PARC, PDGF-BB, RANTES, SCF, SDF-1, TARC, TGF beta 1, TGF beta 3, TNF alpha, TNF beta
Cytokine arrays are an antibody-pair-based assay, analogous to ELISA, but using a membrane as a substrate rather than a plate. Capture antibodies are supplied arrayed/spotted on a membrane with each pair of spots representing a different analyte. Sample is added (0.2-1ml of 1 sample to each membrane), and then paired biotinylated detector antibodies and streptavidin HRP. The cytokine array is analyzed using the same methods as a chemiluminescent western blot. Comparison between samples can be by eye or using densitometry software for a semi-quantitative comparison.
Tested applicationsSuitable for: Multiplex Protein Detectionmore details
Storage instructionsStore at -20°C. Please refer to protocols.
Components 1 x 4 Membranes 1 x 8 Membranes 1 x 2 Membranes 1,000X HRP-Conjugated Streptavidin 1 x 50µl 1 x 50µl 1 x 50µl 1X Blocking Buffer 1 x 25ml 2 x 25ml 1 x 25ml 20X Wash Buffer I 1 x 10ml 1 x 20ml 1 x 10ml 20X Wash Buffer II 1 x 10ml 1 x 20ml 1 x 10ml 2X Cell Lysis Buffer 1 x 10ml 1 x 16ml 1 x 10ml 8-Well Incubation Tray (with Lid) 1 unit 1 unit 1 unit Biotinylated Antibody Cocktail (C6) 2 vials 4 vials 2 vials Detection Buffer C 1 x 1.5ml 1 x 2.5ml 1 x 1.5ml Detection Buffer D 1 x 1.5ml 1 x 2.5ml 1 x 1.5ml Human Cytokine Antibody Array Membranes (C6) 4 units 8 units 2 units
Our Abpromise guarantee covers the use of ab169817 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
|Multiplex Protein Detection||Use at an assay dependent concentration.|
Left image: Conditioned media from MCF-7 cells cultured in 2D; right image: Conditioned media from MCF-7 cells cultured in 3D”
The array was used to examine the potential differences in cytokine profile expression in 2D and 3D culture breast cancer cells (MCF-7), which may account for the significant upregulation of hepcidin (an iron export regulatory protein) observed in 3D culture. Experiments were performed according to the manufacturer’s instructions for the array, using cell lysate and conditioned media. Samples and biotin-conjugated anti-cytokines were incubated overnight at 4°C. Since many cytokines were detected at low levels when imaged, a comparison between 2D and 3D culture was not conclusive. Conditioned media and cell lysates yielded similar results.”
Rating : 4/5. Product is recommended to anyone seeking information on production of a broad range of cytokines. Product is very easy to use.
Verified user: Nicole Blanchette, Graduate Assistant, Molecular Biology & Biophysics, UConnHealth, Farmington, CT, USA.
Left image: Conditioned media from iPSC-derived astrocytes; right image: Media only control.
Samples were incubated overnight at 4C as recommended and included the large volume wash. Images were captured using CCD camera for the exposure times indicated on the image.
Rating 5/5. Simple, sensitive and accurate method to detect multiple cytokines and growth factors from a single sample. The membranes were also consistent across the batch which allowed me to test several samples in parallel. Highly recommended.
ab169817 has not yet been referenced specifically in any publications.