Labelling Review row-Online
Labelling Review row-Online
Labelling Review row-Online
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Primary Antibodies<br />
Cytokeratin, Multi (5/6/8/18)<br />
Clone 5D3, Clone LP34 cocktail<br />
1 mL, 0.1 mL lyophilized NCL-CK5/6/8/18 F P (Enzyme)<br />
1 mL liquid NCL-L-CK5/6/8/18 F P (Enzyme)<br />
7 mL ready-to-use RTU-CK5/6/8/18 F P (Enzyme)<br />
See also Multi-Cytokeratin (5/6/8/18) on page 137.<br />
Cytomegalovirus Antibodies<br />
Clone 2, Clone 6 cocktail<br />
1 mL, 0.1 mL lyophilized Cytomegalovirus (pp65 antigen)<br />
NCL-CMVpp65 P (HIER) W I<br />
Clone QB1/42<br />
1 mL lyophilized Cytomegalovirus (early antigen)<br />
NCL-CMV-EA F P (HIER)<br />
Clone QB1/06<br />
1 mL lyophilized Cytomegalovirus (late antigen)<br />
NCL-CMV-LA F P (HIER)<br />
Cytomegalovirus (CMV) is an opportunistic pathogen infecting lung, kidney,<br />
gut and other organs in situations where an individual is immunologically<br />
immature, such as the fetus and neonate. Infection also occurs in immunosuppressed<br />
individuals eg transplant recipients, individuals undergoing<br />
chemotherapy and those with HIV infection. The typical course of an active<br />
CMV infection in the immunosuppressed individual is reported to be<br />
characterized by a period of pp65 antigenaemia which correlates with viral<br />
replication. This may be observed over some weeks and begins before the<br />
onset of clinical symptoms. Following the isolation of CMV strains in cell<br />
culture, early viral proteins are expressed in the cell nucleus, within 3 to 24<br />
hours of infection. After 48 to 72 hours, a number of late viral proteins may<br />
be demonstrated in the nucleus and cytoplasm of infected cells.<br />
Product Specific Information<br />
NCL-CMVpp65 is a pool of 2 unique monoclonal antibodies suitable for the<br />
detection of the pp65 antigen in cytospin preparations.<br />
Antigenaemia positive peripheral polymorphonuclear leukocytes: immunofluorescence for<br />
Cytomegalovirus pp65 antigen using NCL-CMVpp65. Note characteristic nuclear staining.<br />
Formalin/sucrose-fixed cytospin preparation.<br />
/ 100<br />
For detailed information on all products please visit our website:<br />
www.leica-microsystems.com<br />
Daxx<br />
Clone 36H11<br />
1 mL lyophilized NCL-DAXX P (HIER)<br />
Daxx binds the death domain of Fas and links this receptor to an apoptosis<br />
pathway involving the activation of Jun N-terminal kinase (JNK). The human<br />
homolog of Daxx enhances Fas-mediated apoptosis probably by modulating<br />
the transcription of genes involved in Fas-induced caspase activation and<br />
apoptosis. The Fas-binding domain of Daxx is a dominant negative inhibitor<br />
of both Fas-induced apoptosis and JNK inactivation, while the FADD death<br />
domain partially inhibits death but not JNK activation. The Daxx apoptotic<br />
pathway is sensitive to both bcl-2 and dominant negative JNK pathway<br />
components and acts cooperatively with the FADD pathway. Therefore,<br />
Daxx and FADD define two distinct pathways downstream of Fas. Daxx<br />
mRNA is widely expressed in human tissues such as heart, brain, lung, liver,<br />
skeletal muscle, kidney, pancreas and placenta. The human Daxx gene has<br />
been mapped to 6p21.3 in the major histocompatibility complex (MHC)<br />
region. Its location may help in understanding the genetic basis of autoimmune<br />
diseases. In cells, the protein is found in the nucleus and to a lesser<br />
extent in the cytoplasm.<br />
Human breast carcinoma: immunohistochemical staining for Daxx using NCL-DAXX. Note<br />
cytoplasmic and occasional nuclear staining. Paraffin section.<br />
DEC-205 (CD205)<br />
Clone 11A10<br />
1 mL liquid NCL-L-DEC205 P (HIER) P (HIER)<br />
See also CD205 (DEC-205) on page 88.<br />
Products in this catalog are subject to regulatory approval.<br />
This catalog is not for use in the USA.