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QF0159 Marketing Release Record

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Novocastra Topoisomerase II Alpha<br />

Clone 3F6<br />

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

Antigen Background<br />

Topoisomerase II alpha is an essential nuclear enzyme involved in DNA<br />

replication and is a target for many anti-cancer drugs used for cancer<br />

therapy. Decreased expression of topoisomerase II alpha is the predominant<br />

mechanism of resistance to several chemotherapeutic agents. A significant<br />

variation in the range of expression of this protein has been reported in many<br />

different tumors. Reports of the analysis of primary breast tumors have<br />

indicated that topoisomerase II beta is more widely expressed than<br />

topoisomerase II alpha. Topoisomerase II alpha expression and activity is<br />

linked to the cell cycle and is associated with the proliferation status of cells.<br />

Human bladder tumor: immunohistochemical staining for topoisomerase II alpha using<br />

NCL-TOPOIIA. Note intense nuclear staining of malignant cells and occasional mitotic<br />

figures. Paraffin section.<br />

Novocastra Toxoplasma gondii P30<br />

Antigen<br />

Clone TP3<br />

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

RUO*<br />

Toxoplasma gondii is a ubiquitous protozoan parasite which can infect<br />

healthy humans, often asymptomatically, but may also cause severe<br />

congenital defects in the fetus and life-threatening infection in<br />

immunocompromised hosts. It has been shown that P30, also referred to as<br />

SAG-1, the major surface antigen of Toxoplasma gondii tachyzoites is<br />

involved in the first steps of invasion. This antigen has been reported to have<br />

generated interest as a potential subunit for vaccine production. P30 is a<br />

highly conserved antigen between most strains of Toxoplasma gondii.<br />

Infected human brain: immunohistochemical staining for Toxoplasma gondii P30 antigen using<br />

NCL-TG. Note staining of the parasites in infected areas. Paraffin section.<br />

IVD<br />

Novocastra Transforming Growth Factor<br />

Beta<br />

Clone TGFB17<br />

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

Transforming growth factor beta (TGFB) is a potent cell regulatory<br />

polypeptide homodimer of 25 kD. It variably affects cell growth, differentiation<br />

and other aspects of cellular metabolism such as extracellular matrix<br />

production. Its effect depends upon the cell type and other growth factors<br />

present but in general, TGFB inhibits the growth of epithelial cells and<br />

stimulates the growth of mesenchymal cells. Most breast lesions, benign<br />

and malignant, involve abnormal proliferation and altered architecture of<br />

stromal and/or epithelial elements. Inflammatory cells present in the earliest<br />

lesions of progressive systemic sclerosis (PSS) are reported to release<br />

TGFB possibly resulting in chemotactic recruitment of additional chronic<br />

inflammatory cells. Platelets, a rich source of TGFB, are known to exhibit<br />

aggregability and may contribute to the etiology of PSS.<br />

Human breast carcinoma: immunohistochemical staining for transforming growth factor beta<br />

using NCL-TGFB. Note cytoplasmic staining of tumor cells. Paraffin section.<br />

Novocastra Transforming Growth Factor<br />

Beta Receptor (Type 1)<br />

Clone 8A11<br />

1 mL lyophilized NCL-TGFBR1 P (HIER)<br />

RUO*<br />

RUO*<br />

Transforming growth factor beta (TGFB) is a potent cell regulatory<br />

polypeptide homodimer of 25 kD. It variably affects cell growth, differentiation<br />

and other aspects of cellular metabolism such as extracellular matrix<br />

production. Its effect depends upon the cell type and other growth factors<br />

present but in general, TGFB inhibits the growth of epithelial cells and<br />

stimulates the growth of mesenchymal cells. Most breast lesions, benign<br />

and malignant, involve abnormal proliferation and altered architecture of<br />

stromal and/or epithelial elements. Platelets, a rich source of TGFB, are<br />

known to exhibit aggregability and may contribute to the etiology of PSS.<br />

Human colon, ulcerative colitis: immunohistochemical staining for transforming growth factor<br />

beta receptor (type 1) using NCL-TGFBR1. Note membrane staining of a proportion of epithelial<br />

cells and lymphocytes. Paraffin section.<br />

F Frozen I Immunofluorescence E Electron microscopy<br />

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

W Western blotting<br />

/ 107<br />

Primary Antibodies

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