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Nanog [MD204R]
Description Nanog is a homeodomain-containing transcription factor that is involved in the maintenance of pluripotency and self renewal in embryonic stem cells. Nanog expression is controlled by a network of factors including Sox2 and the key pluripotency regulator Oct-4. Recent advances in somatic cell reprogramming have utilized viral expression of combinations of transcription factors including nanog, Oct-4, Sox2, KLF4, c-Myc, and LIN28. Studies show that Nanog expression can be absent in normal adult organ tissues, but presented in undifferentiated germ cell tumors such as seminoma, dysgerminoma and embryonal carcinoma. Nanog may be used as an aid in the determination of undifferentiated tumors of germ cell origin from non-germ cell tumors (Shipping Cost: €200.00) Host Rabbit Application Immunohistochemistry (IHC) Reactivity Human -
Selenoprotein P/SEPP1 [B9]
Description Selenium is an essential trace element that is incorporated as selenocysteine into the primary structure of selenoproteins. Nutritional deficiency of selenium decreases selenoprotein concentrations and leads to pathologic conditions. Selenoprotein P (SEPP1) is a major selenoprotein that is not a member of those families. It is an extracellular glycoprotein that is present in several isoforms and is the only selenoprotein known to contain multiple selenocysteine residues. A growing body of evidence relates selenium to cancer prevention, immune system function, male fertility, cardiovascular disorder, control of the aging and neurodiseases process. Selenoproteins are thought to be responsible for the majority of these biomedical effects of selenium. It has been also implicated in the regulation of signaling pathways through catalysis of thiol/disulfide exchange. (Shipping Cost: €200.00) Host Mouse Application Immunohistochemistry (IHC) Reactivity Human -
Selenoprotein P/SEPP1 [B9]
Description Selenium is an essential trace element that is incorporated as selenocysteine into the primary structure of selenoproteins. Nutritional deficiency of selenium decreases selenoprotein concentrations and leads to pathologic conditions. Selenoprotein P (SEPP1) is a major selenoprotein that is not a member of those families. It is an extracellular glycoprotein that is present in several isoforms and is the only selenoprotein known to contain multiple selenocysteine residues. A growing body of evidence relates selenium to cancer prevention, immune system function, male fertility, cardiovascular disorder, control of the aging and neurodiseases process. Selenoproteins are thought to be responsible for the majority of these biomedical effects of selenium. It has been also implicated in the regulation of signaling pathways through catalysis of thiol/disulfide exchange. (Shipping Cost: €200.00) Host Mouse Application Immunohistochemistry (IHC) Reactivity Human -
TCR γ/δ (TCR gamma/delta) [H41]
Description T-cell receptor (TCR), a heterodimer composed of either α and β or γ and δ chains, recognizes foreign antigens and translates such recognition events into intracellular signals that elicit a change in the cell from a dormant to an activated state. TCR recognition of self-peptides has been linked to autoimmune disease. Mutant self-peptides have been associated with tumors. Most human T cells (95%) express the α/β or either CD4 or CD8 molecule (single positive, SP), while 2-5% express the γ/δ. However, a small number of T cells lack both CD4 and CD8 (double negative, DN). T helper cells express CD4 proteins and T cytotoxic cells display CD8. Increased percentages of α/β DN T cells have been identified in some autoimmune and immunodeficiency disorders. γ/δ T cells are primarily found within the epithelium. They show less TCR diversity and recognize antigens differently than α/β T cells. Subsets of γ/δ T cells have shown antitumor and immunoregulatory activity. (Shipping Cost: €200.00) Host Mouse Application Immunohistochemistry (IHC) Reactivity Human -
TCR γ/δ (TCR gamma/delta) [H41]
Description T-cell receptor (TCR), a heterodimer composed of either α and β or γ and δ chains, recognizes foreign antigens and translates such recognition events into intracellular signals that elicit a change in the cell from a dormant to an activated state. TCR recognition of self-peptides has been linked to autoimmune disease. Mutant self-peptides have been associated with tumors. Most human T cells (95%) express the α/β or either CD4 or CD8 molecule (single positive, SP), while 2-5% express the γ/δ. However, a small number of T cells lack both CD4 and CD8 (double negative, DN). T helper cells express CD4 proteins and T cytotoxic cells display CD8. Increased percentages of α/β DN T cells have been identified in some autoimmune and immunodeficiency disorders. γ/δ T cells are primarily found within the epithelium. They show less TCR diversity and recognize antigens differently than α/β T cells. Subsets of γ/δ T cells have shown antitumor and immunoregulatory activity. (Shipping Cost: €200.00) Host Mouse Application Immunohistochemistry (IHC) Reactivity Human -
TRPS1 [EPR16171]
Description Trichorhinophalangeal syndrome I (TRPS1), a transcriptional repressor, binds specifically to GATA sequences and represses expression of GATA-regulated genes at selected sites and stages in vertebrate development. Regulates chondrocyte proliferation and differentiation. Executes multiple functions in proliferating chondrocytes, expanding the region of distal chondrocytes, activating proliferation in columnar cells and supporting the differentiation of columnar into hypertrophic chondrocytes. Defects in TRPS1 are the cause of tricho-rhino-phalangeal syndrome type 1. TRPS1 binds to the NuRD complex via CHD4 and can repress other key transcription factors such as p63 and estrogen receptor. It is expressed at higher levels in androgen-dependent prostate cancers, reducing the expression of PSA. (Shipping Cost: €200.00) Host Rabbit Application Flow cytometry (FC), Immunohistochemistry (IHC), Immunoprecipitation (IP), Western Blot (WB) Reactivity Human, Monkey -
TRPS1 [EPR16171]
Description Trichorhinophalangeal syndrome I (TRPS1), a transcriptional repressor, binds specifically to GATA sequences and represses expression of GATA-regulated genes at selected sites and stages in vertebrate development. Regulates chondrocyte proliferation and differentiation. Executes multiple functions in proliferating chondrocytes, expanding the region of distal chondrocytes, activating proliferation in columnar cells and supporting the differentiation of columnar into hypertrophic chondrocytes. Defects in TRPS1 are the cause of tricho-rhino-phalangeal syndrome type 1. TRPS1 binds to the NuRD complex via CHD4 and can repress other key transcription factors such as p63 and estrogen receptor. It is expressed at higher levels in androgen-dependent prostate cancers, reducing the expression of PSA. (Shipping Cost: €200.00) Host Rabbit Application Flow cytometry (FC), Immunohistochemistry (IHC), Immunoprecipitation (IP), Western Blot (WB) Reactivity Human, Monkey