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Mesothelin<br />

Clone 5B2<br />

1 mL lyophilized NCL-MESO F P (HIER)<br />

1 mL liquid NCL-L-MESO F P (HIER)<br />

7 mL ready-to-use RTU-MESO F P (HIER)<br />

7 mL Bond ready-to-use PA0373 P (HIER)<br />

Mesothelin is a glycosyl-phosphatidylinositol-linked (GPI) glycoprotein of<br />

40 kD present on the surface of mesothelial cells, mesotheliomas, epithelial<br />

ovarian cancers and some squamous cell carcinomas. It is synthesized as a<br />

69 kD precursor which is enzymatically processed into an N-terminal<br />

secreted form of 30 kD and the GPI-linked membrane-bound form of 40 kD.<br />

The secreted form is identical to the megakaryocyte potentiating factor, but<br />

it is the GPI-linked membrane-bound form which has generated interest.<br />

Mesothelin is abundantly expressed in the kidney and in occasional<br />

epithelial cells of the trachea, tonsil and fallopian tube. The function of<br />

mesothelin is unclear but it may have a role in cellular adhesion. Mesothelin<br />

is reported to be abundant in the normal mesothelial cells from which<br />

malignant mesotheliomas and ovarian cystadenocarcinomas are derived.<br />

Refer to page 33 for the Bond ready-to-use format.<br />

Human mesothelioma: immunohistochemical staining for mesothelin using NCL-MESO.<br />

Note intense membrane staining of tumor cells. Paraffin section.<br />

Microphthalmia Transcription Factor<br />

(MITF)<br />

Clone 34CA5<br />

1 mL lyophilized NCL-MITF F P (HIER)<br />

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

Microphthalmia transcription factor (MITF) gene product, a nuclear<br />

transcription factor of the basic-helix-loop-helix type, is thought to play a<br />

role in the regulation of genes encoding the enzymes necessary for<br />

melanogenesis. These include tyrosinase, TRP-1 and TRP-2. MITF is critical<br />

for the embryonic development and postnatal viability of melanocytes. The<br />

melanocyte-specific isoform of microphthalmia transcription factor MITF-M,<br />

is reported to be expressed in normal and malignant melanocytes. The other<br />

isoforms, MITF-A, MITF-C and MITF-H, differ structurally at the N-terminus<br />

from MITF-M.<br />

Product Specific Information<br />

Clone 34CA5 is reported to be reactive with the MITF-M isoform.<br />

Human malignant melanoma: immunohistochemical staining for microphthalmia transcription<br />

factor using NCL-L-MITF. Note nuclear staining of melanoma cells. Paraffin section.<br />

Minichromosome Maintenance Protein<br />

Antibodies<br />

Clone CRCT2.1<br />

1 mL, 0.1 mL lyophilized Minichromosome Maintenance<br />

Protein 2 NCL-MCM2 P (HIER)<br />

Clone JCC07<br />

1 mL lyophilized Minichromosome Maintenance<br />

Protein 3 NCL-MCM3 P (HIER)<br />

Clone CRCT5.1<br />

1 mL lyophilized Minichromosome Maintenance<br />

Protein 5 NCL-MCM5 P (HIER) W<br />

Clone DCS-141.1<br />

1 mL lyophilized Minichromosome Maintenance<br />

Protein 7 NCL-MCM7 P (HIER) W<br />

Minichromosome maintenance (MCM) proteins have been reported to play<br />

an essential part in eukaryotic DNA replication. Each of the MCM proteins<br />

have DNA-dependent ATPase motifs in their central domain which are<br />

conserved from yeast to mammals. Both ATPase activity and helicase<br />

activity, which displaces oligonucleotides annealed to single-stranded<br />

circular DNA, are associated with an MCM protein complex. Levels of MCM<br />

proteins generally increase in a variable manner as normal cells progress<br />

from G0 into G1/S phase of the cell cycle. In the G0 phase, MCM2 and MCM5<br />

proteins are reported to be much less abundant than the MCM7 and MCM3<br />

proteins. Therefore, MCM proteins are not present in stoichiometric<br />

amounts and only a proportion of the molecules actively participate in cell<br />

cycle regulation as part of MCM complexes. Oncoprotein E6 of the human<br />

papillomavirus (HPV), associated with cervical cancer (HPV-16 and -18),<br />

degrades the tumor suppressor protein p53, but also seems to have p53independent<br />

transforming functions. E6 was reported to bind to the Cterminal<br />

region of the human MCM7 protein causing chromosomal<br />

abnormalities in human cells expressing E6 proteins of oncogenic HPVs.<br />

Product Specific Information<br />

NCL-MCM2, NCL-MCM3, NCL-MCM5 and NCL-MCM7 are specific for<br />

minichromosome maintenance proteins 2, 3, 5 and 7, respectively.<br />

F Frozen I Immunofluorescence E Electron microscopy<br />

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

W Western blotting<br />

/ 133<br />

Primary Antibodies

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