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96-Well Plate
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48-602MAG
Buffer Detection Kit for Magnetic Beads
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ECM335
Sigma-AldrichHuman sICAM-1 ELISA
This Human sICAM-1 ELISA is used to measure & quantify sICAM-1 levels in Inflammation & Immunology & Neuroscience research.
More>>This Human sICAM-1 ELISA is used to measure & quantify sICAM-1 levels in Inflammation & Immunology & Neuroscience research. Less<<
Human sICAM-1 ELISA: SDB (Sicherheitsdatenblätter), Analysenzertifikate und Qualitätszertifikate, Dossiers, Broschüren und andere verfügbare Dokumente.
Intercellular Adhesion Molecule-1 (ICAM-1) is a member of the immunoglobulin supergene family [Rothlein et al., 1988] and functions as a ligand for integrin alphaLbeta2 or Lymphocyte Function-Associated Antigen-1 (LFA-1), a member of the leukocyte integrin family [Marin & Springer 1987] which mediates lymphocyte adhesion.
ICAM-1 is a single-chain glycoprotein with a polypeptide core of 55kDa expressed on non-hematopoietic cells of many lineages including vascular endothelial cells, thymic epithelial cells, other epithelial cells and fibroblasts, and on hematopoietic cells such as tissue macrophages, mitogen-stimulated T-lymphoblasts, germinal center B-cells and the dendritic cells from tonsils, lymph nodes and Peyer's patches. ICAM-1 is inducible on fibroblasts and endothelial cells by the inflammatory mediators IL-1, TNF and IFN-gamma. Its presence correlates with infiltration of lymphocytes into inflammatory lesions [Dustin et al., 1989; Prober et al., 1986; Rothlein et al., 1986]. ICAM-1 seems to be the initial marker of inflammatory reactions and is expressed prior to and to a greater extent than HLA-DR.
The role of ICAM-1 as a disease marker has been demonstrated for a number of different pathologies, including allergic rhinitis, allergic contact dermatitis [Vejlsgaard et al. 1989], gastrointestinal and bladder cancer, lymphoproliferative disorders [Lal et al., 1992; Rothlein et al., 1991], melanoma [Altomone et al., 1992; Becker et al., 1992; harning et al., 1991], HIV-1 infection [Most et al., 1993], malaria, tissue or organ transplant rejection [Adams et al., 1989; Adams et al., 1993], diabetes mellitus [Lampeter et al., 1992], glomerulonephritis, asthma [Wegner et al., 1990], rheumatoid arthritis [Popocnik et al., 1990] and psoriasis [Lisby et al., 1989].
A panel of 50 sera from healthy blood donors (male and female) was tested for sICAM-1. The detected sICAM levels ranged between 129.9 and 297.4 ng/ml with a mean of 230.3 ng/ml and a standard deviation of 47.4 ng/ml. Normal sICAM-1 levels may vary depending on the serum collective used ranging up to 400ng/ml or greater. Depending upon the study population ranges from 219ng/ml to 1050ng/ml have been reported in the literature.
Analytical Sensitivity and Detection Limits:
Sensitivity:3.3 ng/mL
Range of Detection: 6.25-100 ng/mL
Intra-Assay Variation:4.1%
Inter-Assay Variation:7.7%
Recovery:98.6% average
Assay Time: 75 minutes
Crossreactivity: no interference from soluble TNF-R (60 or 80 kDa), IL-8/NAP-1, TNF-alpha, TNF-beta, IFN-gamma, IFN-alpha2C, IFN-w, IL-6, IL-2R, E-selectin-1 or L-selectin-1.
The ICAM-1 ELISA is an enzyme-linked immunosorbent assay for quantitative detection of soluble Intercellular Adhesion Molecule-1 in cell culture supernatants, serum, plasma, or other biological fluids. The ICAM-1 ELISA is for research use only. Not for use in diagnostic procedures.
Test Principle:
An anti-ICAM-1 monoclonal antibody is adsorbed onto microwells. The pair of monoclonal antibodies use in this ELISA assay detect the soluable form of ICAM-1 present in serum, plasma or other biological fluids.
Soluble ICAM-1 present in a sample or standard then binds to antibodies adsorbed to the microwells. A second, HRP-conjugated monoclonal anti-ICAM-1 antibody is added and binds to ICAM-1 captured by the first antibody.
Unbound enzyme-conjugated anti-ICAM-1 is removed with a wash step and HRP substrate solution is added to the wells.
An amount of colored product is formed, proportional to the amount of soluble ICAM-1 present in the sample. The reaction is terminated by addition of acid and absorbance is measured at 450nm. A standard curve is prepared from five ICAM-1 standard dilutions and the ICAM-1 sample concentration is determined.
Application:
The ICAM-1 ELISA is an enzyme-linked immunosorbent assay for quantitative detection of soluble Intercellular Adhesion Molecule-1 in cell culture supernatants, serum, plasma, or other biological fluids. The ICAM-1 ELISA is for research use only. Not for use in diagnostic procedures.
Alternate Names
CD54
Materials Required but Not Delivered
- 5 mL and 10 mL graduated pipettes
- 5 μL to 1000 μL adjustable single channel micropipettes with
disposable tips
- 50 μL to 300 μL adjustable multichannel micropipette with disposable tips
- Multichannel micropipette reservoir
- Beakers, flasks, cylinders necessary for preparation of reagents
- Device for delivery of wash solution (multichannel wash bottle or
automatic wash system)
- Microwell strip reader capable of reading at 450 nm (620 nm as
optional reference wavelength)
- Glass-distilled or deionized water
- Statistical calculator with program to perform linear regression
analysis.
References
Product Information
Components
· 1 aluminum pouch with Microwell plate coated with Monoclonal Antibody (murine) to human ICAM-1
ICAM1 (CD54) is typically expressed on endothelial cells and cells of the immune system. ICAM1 binds to integrins of type CD11a / CD18, or CD11b / CD18. ICAM1 is also exploited by Rhinovirus as a receptor.
FUNCTION: SwissProt: P05362 # ICAM proteins are ligands for the leukocyte adhesion protein LFA-1 (integrin alpha-L/beta-2). In case of rhinovirus infection acts as a cellular receptor for the virus. Also acts as receptor for some coxsackieviruses. SIZE: 532 amino acids; 57825 Da SUBUNIT: Interacts with human herpesvirus 8 MIR2 protein (Probable). SUBCELLULAR LOCATION: Membrane; Single-pass type I membrane protein. PTM: Monoubiquitinated, which is promoted by MARCH9 and leads to endocytosis. SIMILARITY: SwissProt: P05362 ## Belongs to the immunoglobulin superfamily. ICAM family. & Contains 5 Ig-like C2-type (immunoglobulin-like) domains.
Physicochemical Information
Dimensions
Materials Information
Toxicological Information
Safety Information according to GHS
Safety Information
Product Usage Statements
Usage Statement
Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
Storage and Shipping Information
Storage Conditions
Store kit reagents, except the control, between 2° and 8°C. Store the lyophilized control at -20°C. Immediately after use remaining reagents should be returned to cold storage (2° to 8°C) with the exception of reconstituted control (-20°C). Expiration date of the kit is stated on outside label.
Precautions:
· Reagents are intended for research use only and are not for use in diagnostic or therapeutic procedures.
· Do not mix or substitute reagents with those from other lots or other sources.
· Do not use kit reagents beyond expiration date on label.
· Do not expose kit reagents to strong light during storage or
incubation.
· Rubber or disposable latex gloves should be worn while handling kit reagents or specimens.
· Some reagents contain thimerosal as preservative, which is highly toxic by inhalation, ingestion, or contact with skin. Thimerosal is a possible mutagen and should be handled accordingly.
· Avoid contact of substrate solutions with oxidizing agents and metal.
· In order to avoid microbial contamination or cross-contamination of reagents or specimens which may invalidate the test use disposable pipette tips and/or pipettes.
· Use clean, dedicated reagent trays for dispensing the conjugate and substrate reagents.
· Exposure to acids will inactivate the conjugate.
· Glass-distilled water or deionized water must be used for reagent
preparation.
· Substrate solutions must be at room temperature prior to use.
· Since exact conditions may vary from assay to assay, a standard
curve must be established for every run.
· Bacterial or fungal contamination of either screen samples or reagents or cross-contamination between reagents may cause erroneous results.
· Disposable pipette tips, flasks or glassware are preferred. Reusable glassware must be washed and thoroughly rinsed of all detergents before use.
· Improper or insufficient washing at any stage of the procedure will result in either false positive or false negative results. Completely empty wells before dispensing fresh Wash Buffer, fill with Wash Buffer as indicated for each wash cycle and do not allow wells to sit uncovered or dry for extended periods.
· The use of radioimmunotherapy has significantly increased the number of patients with human anti-mouse IgG antibody (HAMA). HAMA may interfere with assays utilizing murine monoclonal antibodies leading to both false positive and false negative results. HAMA interference can be reduced by adding murine immunoglobulins (serum, ascitic fluid, or monoclonal antibodies of irrelevant specificity) to the Sample Diluent.
Packaging Information
Material Size
1 kit
Transport Information
Supplemental Information
Specifications
Global Trade Item Number
Bestellnummer
GTIN
ECM335
04053252014710
Documentation
Literatur
Übersicht
Pub Med ID
Kinetics and characterization of intercellular adhesion molecule-1 (ICAM-1) expression on keratinocytes in various inflammatory skin lesions and malignant cutaneous lymphomas. Vejlsgaard, G L, et al. J. Am. Acad. Dermatol., 20: 782-90 (1989)
1988
The kinetics of expression of the intercellular adhesion molecule-1 (ICAM-1) were studied on keratinocytes in skin biopsy specimens of sensitive persons in whom the haptens were applied in a standardized format for allergic contact dermatitis testing. There was no ICAM-1 expressed on keratinocytes of normal skin; ICAM-1 was induced as early as 4 hours after the application of the patch in some subjects. By 48 hours after the application of the patch, all specimens contained ICAM-1-positive keratinocytes. This was concurrent with a heavy mononuclear cell dermal infiltrate and maximum clinical manifestations. Expression of human lymphocyte antigen (HLA)-DR or other inducible surface proteins on keratinocytes under these conditions was much less frequent. When specimens from primary irritant dermatitis were used, only 1 of 14 cases had keratinocytes expressing ICAM-1 at 48 hours, the time of maximum clinical manifestation. Among benign inflammatory lesions, most cases resembled the allergic patch test specimens in that ICAM-1 was expressed to a large degree on keratinocytes. Again, the expression of HLA-DR was variable. Malignant skin lesions, on the other hand, were much less consistent and generally lower in terms of ICAM-1 expression on keratinocytes. Furthermore, in contrast to the benign cutaneous conditions, some malignant skin lesions contained keratinocytes that expressed class II antigens or other inducible surface proteins in the absence of ICAM-1. These data suggest that ICAM-1 plays a role in the specific immune response by facilitating either antigen presentation or lymphocytic infiltration.
Acute Injury and Chronic Neurodegeneration Antibodies, Immunoassays, & Histological Stains
Millipore offers a range of products for neurodegeneration research: detection & staining of dying neurons. See below for products for products based on the expertise of Upstate & Chemicon. Weitere Informationen >>
ICAM Antibodies & Kits
Millipore’s ICAM Antibodies demonstrate specificity against ICAM or CD54, an adhesion molecule in immune cells. See below for related products for ICAM, based on the expertise of Upstate & Chemicon. Weitere Informationen >>