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Mouse Neural Cell Adhesion Molecule (NCAM) ELISA Kit-Sandwich

Cat. No.EK5F42

Product TypeAnimal Immunoassay Kits

Size

Product Overview

BioVenic Mouse Neural Cell Adhesion Molecule (NCAM) ELISA Kit-Sandwich is designed for the quantitative determination of Mouse NCAM in serum, plasma, tissue homogenate, cell culture supernatant, cell lysate, and other biological fluids using a Sandwich ELISA method. For research use only.

Specifications

Assay Type ELISA-Sandwich
Specificity The assay kit is specific for Mouse Neural Cell Adhesion Molecule (NCAM).
Target Species Mouse
Species Reactivity Mouse
Detection Range 0.17-10 ng/mL
Reproducibility Intra-Assay: CV < 10%; Inter-Assay: CV < 12%
Assay Time Around 90 min
Sample Requirement Serum, plasma, tissue homogenate, cell culture supernatant, cell lysate, and other biological fluids.

Target Information

The Neural Cell Adhesion Molecule (NCAM), also known as CD56, is a glycoprotein that facilitates homophilic binding and is found on the surface of neurons, glia, and skeletal muscle. While CD56 is frequently viewed as a marker of neural lineage commitment because of its initial discovery, it is also expressed in the hematopoietic system, among others. Studies have shown that NCAM plays a role in regulating the pathfinding of thalamocortical axons and the organization of cortical somatosensory representation in mice.

Target/Biomarker Mouse NCAM
Target Synonym CD56; NCAM1; MSK39; N-CAM-1

Shipping and Storage

This product is shipped with gel ice packs. It is recommended to store at 2-8 °C (Up to 6 months).

Documents

COA

To request a Certificate of Analysis, please enter the Lot No. in the search box. Note: Certificate of Analysis not available for kits.

The product is for research use only.
Not for commercial, prophylactic, diagnostic, or therapeutic applications.

References

  1. Enriquez-Barreto, Lilian, et al. "Neural cell adhesion molecule, NCAM, regulates thalamocortical axon pathfinding and the organization of the cortical somatosensory representation in mouse." Frontiers in molecular neuroscience 5 (2012): 76.
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