Mouse myeloma cell line NS0-derived recombinant human ALCAM/CD166 Trp28-Ala526 Accession # AAB59499
Specificity
Detects human ALCAM/CD166 in direct ELISAs and Western blots. In Western blots, no cross-reactivity with recombinant mouse (rm) ALCAM, recombinant human (rh) BCAM, rhTROP-2, rhEpCAM, rhMCAM, rhNCAML1, rmMadCAM, or rmOCAM is observed.
Source
N/A
Isotype
IgG1
Clonality
Monoclonal
Host
Mouse
Gene
ALCAM
Purity Statement
Protein A or G purified from ascites
Innovator's Reward
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ALCAM
(activated leukocyte cell adhesion molecule), designated CD166 and also
called MEMD and SC‑1/DM‑GRASP/BEN in the chicken, is a 100‑110 kDa
type I transmembrane glycoprotein and a member of the Ig CAM family
within the immunoglobulin superfamily (1). ALCAM is expressed on thymic
epithelium, microvascular endothelium, activated lymphocytes and
monocytes, and monocyte‑derived dendritic cells (1, 2). Human ALCAM cDNA
encodes 583 amino acid (aa), including signal peptide (27 aa),
extracellular domain (ECD, 500 aa) with two V‑type and three C2‑type
Ig‑like domains, transmembrane (22 aa) and cytoplasmic (34 aa) domains
(1). Human ALCAM ECD shares 93%, 95% and 96% aa sequence identity with
mouse/rat, bovine and porcine/equine ALCAM, respectively. A 570 aa
isoform lacks aa 503‑515, while a 555 aa form lacks most of the
cytoplasmic domain. A secreted isoform in endothelial cells that is
truncated at aa 133 (sALCAM) antagonizes full‑length ALCAM (3, 4). ALCAM
mediates low‑affinity adhesion with itself or the cysteine‑rich
scavenger receptor CD6 to regulate T cell development, immunological
synapses (IS), and cell migration through endothelial junctions (1‑11).
ALCAM on thymic epithelia mediates adhesion to CD6 on CD4+CD8+
T cells (6). Adhesion of ALCAM‑expressing antigen presenting cells and
CD6‑expressing T cells stabilizes the early IS, while later it enhances
CD3 effects on T cell proliferation, CD25 expression, and Th1 commitment
(2, 7, 8). High ALCAM expression at the blood‑brain barrier in active
multiple sclerosis, and its mouse model (EAE), promotes leukocyte
migration to the brain (8, 9). High ALCAM expression on melanoma cell
lines appears to be pro‑metastatic, but anti‑metastatic activity has
been reported in breast cancer (3, 10, 11). ALCAM may influence
expression or adhesion of the neuronal adhesion molecule NCAM‑L1, both
in the developing retina and invasive melanoma (3, 12).
Bowen, M.A. et al. (1995) J. Exp. Med. 181:2213.
Zimmerman, A.W. et al. (2006) Blood 107:3212.
van Kilsdonk, J.W.J. et al. (2008) Cancer Res. 68:3671.
Ikeda, K. and T. Quertermous (2004) J. Biol. Chem. 279:55315.
van Kempen, L.C. et al. (2001) J. Biol. Chem. 276:25783.
Castro, M.A.A. et al. (2007) J. Immunol. 178:4351.
Nair, P. et al. (2010) Clin. Exp. Immunol. 162:116.
Masedunskas, A. et al. (2006) FEBS Lett. 580:2637.
Cayrol, R. et al. (2008) Nat. Immunol. 9:137.
Degen, W.G. et al. (1998) Am. J. Pathol. 152:805.
King, J.A. et al. (2010) Mol. Cancer 9:266.
Buhusi, M. et al. (2009) J. Neurosci. 29:15630.
Limitations
This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.
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