Hľadali ste: 5-Amino-2-fluoropyridine

Katalógové číslo: (BOSSBS-11294R-A350)

Dodávateľ: BIOSS INC

Opis: The Hox homeobox genes encode proteins that are transcriptional regulators with an established role in embryonic development. HoxA6 (homeobox A6), also known as HOX1B, is a 233 amino acid protein that localizes to the nucleus. Expressed during embryonic development, HoxA6 functions as a sequence-specific DNA-binding transcription factor that is part of a regulatory mechanism that provides cells with positional identities during development. Via its ability to bind DNA, HoxA6 plays an important role in the regulation of gene expression, as well as morphogenesis and differentiation. The gene encoding HoxA6 maps to human chromosome 7, which houses over 1,000 genes and comprises nearly 5% of the human genome. Defects in some of the genes localized to chromosome 7 have been linked to Osteogenesis imperfecta, Williams-Beuren syndrome, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome.

Merná jednotka: 1 * 100 µl

Predaj

Katalógové číslo: (BOSSBS-11294R-CY7)

Dodávateľ: BIOSS INC

Opis: The Hox homeobox genes encode proteins that are transcriptional regulators with an established role in embryonic development. HoxA6 (homeobox A6), also known as HOX1B, is a 233 amino acid protein that localizes to the nucleus. Expressed during embryonic development, HoxA6 functions as a sequence-specific DNA-binding transcription factor that is part of a regulatory mechanism that provides cells with positional identities during development. Via its ability to bind DNA, HoxA6 plays an important role in the regulation of gene expression, as well as morphogenesis and differentiation. The gene encoding HoxA6 maps to human chromosome 7, which houses over 1,000 genes and comprises nearly 5% of the human genome. Defects in some of the genes localized to chromosome 7 have been linked to Osteogenesis imperfecta, Williams-Beuren syndrome, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome.

Merná jednotka: 1 * 100 µl

Predaj

Katalógové číslo: (PROOCIL-PCB-55-C)

Dodávateľ: PROMOCHEM

Opis: 2,3,3',4-Tetrachlorobiphenyl (PCB No. 55)

Merná jednotka: 1 * 5 mg

Predaj

Katalógové číslo: (PROOCIL-PCB-164-C)

Dodávateľ: PROMOCHEM

Opis: 2,3,3',4',5',6-Hexachlorobiphenyl (PCB No. 164)

Merná jednotka: 1 * 5 mg

Predaj

Katalógové číslo: (EHERC20002000)

Dodávateľ: EHRENSTORFER

Opis: 2,3,3'-Trichlorobiphenyl (PCB No. 20)

Merná jednotka: 1 * 10 mg

Predaj

Katalógové číslo: (PROOBCR-290)

Dodávateľ: PROMOCHEM

Opis: 2,3,3'-Trichlorobiphenyl (PCB No. 20)

Merná jednotka: 1 * 25 mg

Predaj

Katalógové číslo: (BOSSBS-11294R-CY3)

Dodávateľ: BIOSS INC

Opis: The Hox homeobox genes encode proteins that are transcriptional regulators with an established role in embryonic development. HoxA6 (homeobox A6), also known as HOX1B, is a 233 amino acid protein that localizes to the nucleus. Expressed during embryonic development, HoxA6 functions as a sequence-specific DNA-binding transcription factor that is part of a regulatory mechanism that provides cells with positional identities during development. Via its ability to bind DNA, HoxA6 plays an important role in the regulation of gene expression, as well as morphogenesis and differentiation. The gene encoding HoxA6 maps to human chromosome 7, which houses over 1,000 genes and comprises nearly 5% of the human genome. Defects in some of the genes localized to chromosome 7 have been linked to Osteogenesis imperfecta, Williams-Beuren syndrome, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome.

Merná jednotka: 1 * 100 µl

Predaj

Katalógové číslo: (BOSSBS-11294R-FITC)

Dodávateľ: BIOSS INC

Opis: The Hox homeobox genes encode proteins that are transcriptional regulators with an established role in embryonic development. HoxA6 (homeobox A6), also known as HOX1B, is a 233 amino acid protein that localizes to the nucleus. Expressed during embryonic development, HoxA6 functions as a sequence-specific DNA-binding transcription factor that is part of a regulatory mechanism that provides cells with positional identities during development. Via its ability to bind DNA, HoxA6 plays an important role in the regulation of gene expression, as well as morphogenesis and differentiation. The gene encoding HoxA6 maps to human chromosome 7, which houses over 1,000 genes and comprises nearly 5% of the human genome. Defects in some of the genes localized to chromosome 7 have been linked to Osteogenesis imperfecta, Williams-Beuren syndrome, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome.

Merná jednotka: 1 * 100 µl

Predaj

Katalógové číslo: (PROOCIL-PCB-57-C)

Dodávateľ: PROMOCHEM

Opis: 2,3,3',5-Tetrachlorobiphenyl (PCB No. 57)

Merná jednotka: 1 * 5 mg

Predaj

Katalógové číslo: (PROOCIL-PCB-110-C)

Dodávateľ: PROMOCHEM

Opis: 2,3,3',4',6-Pentachlorobiphenyl (PCB No. 110)

Merná jednotka: 1 * 5 mg

Predaj

Katalógové číslo: (BOSSBS-6923R)

Dodávateľ: BIOSS INC

Opis: Comprising nearly 4% of human DNA, chromosome 13 contains around 114 million base pairs and 400 genes. Key tumor suppressor genes on chromosome 13 include the breast cancer susceptibility gene, BRCA2, and the RB1 (retinoblastoma) gene. RB1 encodes a crucial tumor suppressor protein which, when defective, leads to malignant growth in the retina and has been implicated in a variety of other cancers. The gene SLITRK1, which is associated with Tourette syndrome, is on chromosome 13. As with most chromosomes, polysomy of part or all of chromosome 13 is deleterious to development and decreases the odds of survival. Trisomy 13, also known as Patau syndrome, is quite deadly and the few who survive past one year suffer from permanent neurologic defects, difficulty eating and vulnerability to serious respiratory infections. The gene encoding CCDC70 (Coiled-coil domain-containing protein 70), a 233 amino acid secreted protein, exists on human chromosome 13.

Merná jednotka: 1 * 100 µl

Predaj

Katalógové číslo: (BOSSBS-9738R-CY5)

Dodávateľ: BIOSS INC

Opis: Mapping to chromosome 21, the FASP1 gene (FAPP1-associated protein 1) encodes a 233 amino acid protein that is homologous to the fission yeast protein Mis18. In yeast, Mis18 is localized to the centrosome and forms a complex with Mis16 to maintain the deacetylated state of histones specifically in the central core of centromeres. FASP1, also known as Protein Mis18-alpha and C21orf45, is required for the recruitment of CENP-A to centrosomes and is thereby essential for normal chromosome segregation during mitosis. With expression in testis, FASP1 exists as a homodimer, a heterodimer with MIS18B or is present in a complex containing other Mis18 family members. FASP1 has been shown to bind to pp5644 in Hela cells, where overexpression of pp5644 leads to inhibited growth and colony formation.

Merná jednotka: 1 * 100 µl

Predaj

Katalógové číslo: (PROOCIL-PCB-58-C)

Dodávateľ: PROMOCHEM

Opis: 2,3,3',5'-Tetrachlorobiphenyl (PCB No. 58)

Merná jednotka: 1 * 5 mg

Predaj

Katalógové číslo: (PROOCIL-PCB-165-C)

Dodávateľ: PROMOCHEM

Opis: 2,3,3',5,5',6-Hexachlorobiphenyl (PCB No. 165)

Merná jednotka: 1 * 5 mg

Predaj

Katalógové číslo: (PROOCIL-PCB-159-C)

Dodávateľ: PROMOCHEM

Opis: 2,3,3',4,5,5'-Hexachlorobiphenyl (PCB No. 159)

Merná jednotka: 1 * 5 mg

Predaj

Katalógové číslo: (PROOCIL-PCB-112-C)

Dodávateľ: PROMOCHEM

Opis: 2,3,3',5,6-Pentachlorobiphenyl (PCB No. 112)

Merná jednotka: 1 * 5 mg

Predaj