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N-Cadherin<br />

Clone IAR06<br />

1 mL, 0.1 mL liquid NCL-L-N-Cad P (HIER)<br />

N-Cadherin is a member of the cadherin family of calcium dependent cell<br />

adhesion molecules. The classical cadherins include the E, N, R, P and VE-<br />

Cadherins which are believed to be expressed in a tissue specific manner.<br />

The classical cadherins have a characteristic structure comprising an extra<br />

cellular calcium-binding domain, consisting of five repeats, a<br />

transmembrane domain and a highly conserved cytoplasmic domain, which<br />

mediates interactions with cytoskeletal components of the cell via<br />

interactions with intracellular proteins including the catenins. Cadherins<br />

play an important role in cell-cell adhesion, and are implicated in<br />

segregation and aggregation of tissues during development. N-Cadherin is<br />

reported to be expressed in various cell types including neural, myocardial<br />

and mesenchymal cells. During tumor progression increased N-Cadherin<br />

expression concomitant with the loss of E-Cadherin expression is one of the<br />

features of the epithelial to mesenchymal transition, which is associated<br />

with increased tumor invasion and poor prognosis. N-Cadherin has been<br />

proposed as a useful marker in a panel of antibodies to differentiate<br />

mesotheliomas from adenocarcinomas.<br />

Human testes: immunohistochemical staining for N-Cadherin using NCL-L-N-Cad. Note<br />

cytoplasmic and membrane staining of sertoli cells. Paraffin section.<br />

NCAM (CD56)<br />

Clone CD564<br />

1 mL, 0.1 mL lyophilized NCL-CD56-564 P (HIER)<br />

Clone 1B6<br />

1 mL, 0.1 mL lyophilized NCL-CD56-1B6 P (HIER) W<br />

1 mL liquid NCL-L-CD56-1B6 P (HIER) W<br />

7 mL ready-to-use RTU-CD56-1B6 P (HIER)<br />

See also CD56 (NCAM) on page 81.<br />

Nerve G<strong>row</strong>th Factor Receptor (gp75)<br />

Clone 7F10<br />

1 mL, 0.1 mL lyophilized NCL-NGFR P (HIER)<br />

Nerve g<strong>row</strong>th factor receptor (NGFR) is a member of the nerve g<strong>row</strong>th factor<br />

(NGF) tumor necrosis factor (TNF) superfamily of receptors. Nerve g<strong>row</strong>th<br />

factor is important for the development, differentiation and survival of neurons<br />

and its action is mediated by the binding of two distinctive cell surface<br />

receptors; the high-affinity NGFR (TrkA ) and the low-affinity NGFR (gp75). The<br />

functional role of gp75 has not yet been fully elucidated. In vitro, unbound<br />

gp75 has been shown to promote neural cell death, whereas, binding of gp75<br />

by NGF ligand or antibody has been shown to inhibit gp75-induced cell death.<br />

NGFR (gp75) is reported to be expressed in neuronal axons, Schwann cells<br />

and perineural cells of peripheral nerves and in non-neural cells that includes<br />

myoepithelial cells of breast, salivary and sweat glands, outer root sheath<br />

cells of hair follicles, adventitia of mature blood vessels and a lymphocyte<br />

subpopulation in the spleen and lymph node. NGFR has also been reported to<br />

be expressed in a proportion of phaeochromocytomas, paragangliomas and<br />

tumors of peripheral nerve sheath differentiation.<br />

Product Specific Information<br />

NCL-NGFR is raised to the gp75 low-affinity NGFR protein.<br />

Human brain, nucleus of Meynert neurons in basal forebrain: immunohistochemical staining<br />

for nerve g<strong>row</strong>th factor receptor (gp75) using NCL-NGFR. Note cytoplasmic and membrane<br />

staining of cholinergic neurons. Paraffin section.<br />

Neuroblastoma Marker<br />

Clone NB84a<br />

1 mL lyophilized NCL-NB84 FPC<br />

Neuroblastoma is a complex malignant disease in children. This tumor of the<br />

sympathetic nervous system, derived from pathologically maturing neural<br />

crest progenitor cells, is unique among pediatric cancers because of<br />

spontaneous regressions and catecholamine excretions. In a major study,<br />

Mietten M et al., indicated the NB84 monoclonal antibody to be a useful<br />

reagent to separate neuroblastoma from other small round cell tumors. Most<br />

of the undifferentiated neuroblastomas in their study (21 of 22) and all 83<br />

differentiated neuroblastomas reacted with NB84, but none of these tumors<br />

were CD99 positive. Compared with synaptophysin, NB84 was more sensitive,<br />

although less specific, in the identification of neuroblastoma in<br />

formaldehyde-fixed tissue. In addition to neuroblastoma, skeletal and<br />

extraskeletal Ewing’s sarcoma and medulloblastoma showed NB84 reactivity<br />

in approximately 20 percent of cases and 50 percent of desmoplastic<br />

small round cell tumors showed positive cells, usually in smaller numbers<br />

than the neuroblastomas. The NB84 reactivity was seen slightly more<br />

commonly in morphologically defined (rosette-positive) cases of peripheral<br />

primitive neuroectodermal tumors than in Ewing’s sarcoma. However, the<br />

NB84 positivity did not correlate with the expression of other neural markers<br />

(neurofilament proteins, CD57, and synaptophysin) in these tumors. All other<br />

small round cell tumors including rhabdomyosarcomas, Wilms’ tumors, and<br />

lymphomas were NB84 negative (Miettinen M et al., Am J Surg Pathol.<br />

22(3):327-32 (1998)).<br />

Product Specific Information<br />

Enzyme pretreatment may enhance staining in some cases.<br />

F Frozen I Immunofluorescence E Electron microscopy<br />

P Paraffin C Flow cytometry O Other applications<br />

W Western blotting<br />

/ 141<br />

Primary Antibodies

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