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UNSPSC Code:
12352203
NACRES:
NA.41
eCl@ss:
32160702
Technique(s):
western blot: suitable, ELISA: suitable, immunofluorescence: suitable, immunohistochemistry: suitable
Conjugate:
unconjugated
Application:
ELISA, IF, IHC, WB
Citations:
132
technique(s)
western blot: suitable, ELISA: suitable, immunofluorescence: suitable, immunohistochemistry: suitable
biological source
rabbit
conjugate
unconjugated
antibody form
affinity purified immunoglobulin
antibody product type
primary antibodies
clone
polyclonal
purified by
affinity chromatography
species reactivity
mouse, rat, chicken, human
manufacturer/tradename
Chemicon®
NCBI accession no.
UniProt accession no.
shipped in
dry ice
target post-translational modification
unmodified
Quality Level
Gene Information
human ... NCAM1(4684)
General description
MW is 200-250 kDa; when treated with Neuraminidase, 140-180 kDa A breakdown product of 160 kDa may also be visible.
The Immunoglobulin superfamily of cell adhesion molecules is related to the immunoglobulins proteins by structure. The family contains over a 100 members, which include ICAM (intercellular adhesion molecule), NCAM (neural cell adhesion molecule) and NgCAM (neural-glial cell adhesion molecule). Both NCAM and NgCAM are calcium independent adhesion molecules. NCAM, the first CAM to be characterized, is expressed on all neurons from very early in development. It binds homophilically to NCAM on adjacent cells and has a variety of functions during neural development. One of these important functions is to hold developing neurites together during neuron outgrowth and formation of neural connections. The adhesive properties of NCAM are modulated during development and plasticity by the presence of the regulated carbohydrate, polysialic acid (PSA). The post-translational addition of alpha-2,8-linked PSA (NCAM-PSA) appears to contribute to synaptic plasticity during learning and memory formation and to the mechanisms of nerve regeneration.
The previously assigned protein identifier P13592 has been merged into P13591. Full details can be found on the UniProt database.
Immunogen
Highly purified chicken NCAM
Application
Immunohistochemistry:
A previous lot was shown to work with a wide range of fixatives. Will detect chicken NCAM using a concentration of 1 μg/mL and mouse NCAM using a concentration of 2 μg/mL.
Immunofluorescence:
A previous lot of this antibody was used in Immunofluorescence.
Function blocking:
A previous lot of this antibody was used in Function blocking.
ELISA:
0.3 μg/mL of a previous lot was used.
Optimal working dilutions must be determined by end user.
A previous lot was shown to work with a wide range of fixatives. Will detect chicken NCAM using a concentration of 1 μg/mL and mouse NCAM using a concentration of 2 μg/mL.
Immunofluorescence:
A previous lot of this antibody was used in Immunofluorescence.
Function blocking:
A previous lot of this antibody was used in Function blocking.
ELISA:
0.3 μg/mL of a previous lot was used.
Optimal working dilutions must be determined by end user.
Research Category
Neuroscience
Neuroscience
Research Sub Category
Growth Cones & Axon Guidance
Growth Cones & Axon Guidance
Detect Neural Cell Adhesion Molecule using this Anti-Neural Cell Adhesion Molecule Antibody validated for use in ELISA, IF, IH, FUNC & WB.
Biochem/physiol Actions
Expected to cross-react with Chicken, Human, and rat.
Neural Cell Adhesion Molecule (NCAM). MW is 200-250 kDa; when treated with Neuraminidase, 140-180 kDa. A breakdown product of 160 kDa may also be visible.
Physical form
ImmunoAffinity Purified
Purified rabbit polyclonal in buffer containing PBS containing no preservatives.
Preparation Note
Stable for 1 year at -20°C from date of receipt.
Handling Recommendations:
Upon first thaw, and prior to removing the cap, centrifuge the vial and gently mix the solution. Aliquot into microcentrifuge tubes and store at -20°C. Avoid repeated freeze/thaw cycles, which may damage IgG and affect product performance.
Handling Recommendations:
Upon first thaw, and prior to removing the cap, centrifuge the vial and gently mix the solution. Aliquot into microcentrifuge tubes and store at -20°C. Avoid repeated freeze/thaw cycles, which may damage IgG and affect product performance.
Analysis Note
Control
Neuraminidase-treated mouse brain membrane.
Neuraminidase-treated mouse brain membrane.
Routinely evaluated by Western Blot on mouse brain lysates.
Western Blot Analysis: 1:1000 dilution of this lot detected NCAM on 10 μg of mouse brain lysate.
Western Blot Analysis: 1:1000 dilution of this lot detected NCAM on 10 μg of mouse brain lysate.
Other Notes
Concentration: Please refer to the Certificate of Analysis for the lot-specific concentration.
Legal Information
CHEMICON is a registered trademark of Merck KGaA, Darmstadt, Germany
Disclaimer
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.
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存储类别
12 - Non Combustible Liquids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
Maria S Skog et al.
Stem cell research & therapy, 7(1), 113-113 (2016-08-17)
In order to develop novel clinical applications and to gain insights into possible therapeutic mechanisms, detailed molecular characterization of human bone marrow-derived mesenchymal stromal cells (hBM-MSCs) is needed. Neural cell adhesion molecule (NCAM, CD56) is a transmembrane glycoprotein modulating cell-cell
Taste bud cells of adult mice are responsive to Wnt/?-catenin signaling: implications for the renewal of mature taste cells.
Gaillard, D; Barlow, LA
Genesis (2000)
Protein kinase A activation promotes plasma membrane insertion of DCC from an intracellular pool: A novel mechanism regulating commissural axon extension.
Bouchard, JF; Moore, SW; Tritsch, NX; Roux, PP; Shekarabi, M; Barker, PA; Kennedy, TE
The Journal of Neuroscience null
Patrick Kellish et al.
The Journal of clinical investigation, 129(6), 2279-2292 (2019-04-30)
Oncolytic virotherapy has been proposed as an ablative and immunostimulatory treatment strategy for solid tumors that are resistant to immunotherapy alone; however, there is a need to optimize host immune activation using preclinical immunocompetent models in previously untested common adult
Olesya Chayka et al.
Journal of the National Cancer Institute, 101(9), 663-677 (2009-04-30)
Clusterin expression in various types of human cancers may be higher or lower than in normal tissue, and clusterin may promote or inhibit apoptosis, cell motility, and inflammation. We investigated the role of clusterin in tumor development in mouse models
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