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MCAM (Melanoma Cell Adhesion Molecule)/MUC18/CD146 Monoclonal Antibody (MCAM/3179)

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Datasheet
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Datasheet
Protocols
Questions & Answers

Cite MCAM (Melanoma Cell Adhesion Molecule)/MUC18/CD146 Monoclonal Antibody (MCAM/3179)

  • Antibody Testing Data (2)
MCAM (Melanoma Cell Adhesion Molecule)/MUC18/CD146 Antibody in Peptide array (ARRAY)
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MCAM (Melanoma Cell Adhesion Molecule)/MUC18/CD146 Antibody in Peptide array (ARRAY)
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MCAM (Melanoma Cell Adhesion Molecule)/MUC18/CD146 Antibody (4162-MSM9-P0) in ARRAY

Analysis of Protein Array containing more than 19,000 full-length human proteins using MCAM Mouse Monoclonal Antibody (MCAM/3179). Z- and S- Score: The Z-score represents the strength of a signal that a monoclonal antibody (MAb) (in combination with a fluorescently-tagged anti-IgG secondary antibody) produces when binding to a particular protein on the HuProtTM array. Z-scores are described in units of stan... View More {{ $ctrl.currentElement.advancedVerification.fullName }} validation info. View more
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MCAM (Melanoma Cell Adhesion Molecule)/MUC18/CD146 Antibody in Peptide array (ARRAY)
MCAM (Melanoma Cell Adhesion Molecule)/MUC18/CD146 Antibody in SDS-PAGE (SDS-PAGE)

Product Details

4162-MSM9-P0

Applications
Tested Dilution
Publications

ELISA (ELISA)

2-4 µg/mL
-

Peptide Array (Array)

Assay-dependent
-
Product Specifications

Species Reactivity

Human

Host/Isotype

Mouse / IgG2c, kappa

Class

Monoclonal

Type

Antibody

Clone

MCAM/3179

Immunogen

Recombinant human MCAM protein

Conjugate

Unconjugated Unconjugated Unconjugated

Form

Liquid

Concentration

200 µg/mL

Purification

Protein A/G

Storage buffer

PBS, pH 7.4, with 0.05% BSA

Contains

0.05% sodium azide

Storage conditions

4°C, do not freeze

Shipping conditions

Wet ice

Target Information

CD146, also known as MCAM (Melanoma Cell Adhesion Molecule), is an integral membrane glycoprotein belonging to the immunoglobulin superfamily. It is heavily glycosylated, with more than 50% of its mass derived from carbohydrates. CD146 is primarily expressed on endothelial cells at cell-cell junctions, playing a crucial role in cell adhesion and the cohesion of the endothelial monolayer in vascular tissue. In addition to endothelial cells, CD146 is expressed on bone marrow fibroblasts, mesenchymal stromal cells, endometrial stromal cells, and some tumors, particularly melanoma. It has also been observed on a subset of circulating T cells and activated lymphocytes, but not on circulating endothelial cells, as indicated by the absence of other endothelial markers such as CD31 and CD51/61. CD146 functions as a calcium-independent cell adhesion molecule and may also act as a signal transduction molecule. It is involved in the recruitment of Fyn kinase and the subsequent tyrosine phosphorylation of intracellular proteins, which are important for actin cytoskeleton assembly. This signaling role includes triggering tyrosine phosphorylation of FYN and PTK2 and causing a transient increase in intracellular calcium concentration. In the context of cancer, CD146 expression may facilitate the interaction of melanoma cells with the vascular system, enhancing hematogenous tumor spread. Additionally, CD146 could serve as an adhesion molecule active in neural crest cells during embryonic development, highlighting its diverse roles in both normal physiological processes and disease states.

For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.

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Bioinformatics

Protein Aliases: CD146; Cell surface glycoprotein MUC18; Cell surface glycoprotein P1H12; Gicerin; melanoma adhesion molecule; Melanoma cell adhesion molecule; Melanoma-associated antigen A32; Melanoma-associated antigen MUC18; S-endo 1 endothelial-associated antigen

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Gene Aliases: CD146; MCAM; MUC18

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UniProt ID: (Human) P43121

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Entrez Gene ID: (Human) 4162

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Process(es)
angiogenesis glomerular filtration cell adhesion anatomical structure morphogenesis positive regulation of cell migration vascular wound healing
It has to be done as per old AB suggested Products section.
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