2-Amino-4-chloro-7-methoxyquinazoline
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
1,4'-Bipiperidine-1'-carboximidamide hydroiodide 97%
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
6-(Bromomethyl)-2,2,3,3-tetrafluoro-1,4-benzodioxane
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
2,3-Dihydro-1,4-benzodioxin-5-carbonsäure
Artikel-Nr:
(APOSOR310995-1G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR310995-1G
Lokale Artikelnummer::
APOSOR310995-1G
Beschreibung:
3-Benzoyl-6,7-dimethoxy-1,4-dihydroquinolin-4-one
VE:
1 * 1 g
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
8-Phenyl-1,4-dioxaspiro[4.5]decane-8-carbaldehyde
Artikel-Nr:
(APOSOR470231-5G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR470231-5G
Lokale Artikelnummer::
APOSOR470231-5G
Beschreibung:
3-(3-Nitrophenyl)-1,4-diazaspiro[4.4]nonan-2-one
VE:
1 * 5 g
Artikel-Nr:
(BOSSBS-13487R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13487R-A680
Lokale Artikelnummer::
BOSSBS-13487R-A680
Beschreibung:
Golgin 245 is also known as p230, GCP2, GOLG or golgi autoantigen and is a 2,230 amino acid protein that is expressed as three isoforms. Golgin 245 is localized to the cytoplasm in cells and is a member of the golgin family, all of which are peripheral membrane proteins associated with the Golgi complex. Golgin 245 has a carboxyl-terminal GRIP domain, which attaches to the trans-Golgi network (TGN) and TGN-derived vesicles. It is thought that the interaction that takes place between golgin 245 and MACF1, which cross-links microtubules to the Actin cytoskeleton, allows proteins to be transported from the TGN to the cell periphery. against golgin 245 are associated with two chronic disorders known as Sjren's syndrome and Hepatitis B.
VE:
1 * 100 µl
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
6-Bromo-3,4-dihydro-2H-1,4-benzoxazine
Lieferant:
Biotium
Beschreibung:
Cytochrome C is a well-characterized mobile electron transport protein that is essential to energy conversion in all aerobic organisms. In mammalian cells, this highly conserved protein is normally localized to the mitochondrial inter-membrane space. More recent studies have identified cytosolic cytochrome c as a factor necessary for activation of apoptosis. During apoptosis, cytochrome c is trans-located from the mitochondrial membrane to the cytosol, where it is required for activation of caspase-3 (CPP32). Overexpression of Bcl-2 has been shown to prevent the translocation of cytochrome c, thereby blocking the apoptotic process. Overexpression of Bax has been shown to induce the release of cytochrome c and to induce cell death. The release of cytochrome c from the mitochondria is thought to trigger an apoptotic cascade, whereby Apaf-1 binds to Apaf-3 (caspase-9) in a cytochrome c-dependent manner, leading to caspase-9 cleavage of caspase-3.
Lieferant:
Biotium
Beschreibung:
Fibroblast growth factor-1 (FGF-1), also designated acidic FGF, and fibroblast growth factor-2 (FGF-2), also designated basic FGF, are members of a family of growth factors that stimulate proliferation of cells of mesenchymal, epithelial and neuroectodermal origin. Additional members of the FGF family include the oncogenes FGF-3 (Int2) and FGF-4 (hst/Kaposi), FGF-5, FGF-6, FGF-7 (KGF), FGF-8 (AIGF), FGF-9 (GAF) and FGF-10 through FGF-23. Members of the FGF family share 30-55% amino acid sequence identity and similar gene structure, and are capable of transforming cultured cells when overexpressed in trans- fected cells. Cellular receptors for FGFs are members of a second multigene family, including four tyrosine kinases designated Flg (FGFR-1), Bek (FGFR-L), TKF and FGFR-3.
Lieferant:
Biotium
Beschreibung:
Fibroblast growth factor-1 (FGF-1), also designated acidic FGF, and fibroblast growth factor-2 (FGF-2), also designated basic FGF, are members of a family of growth factors that stimulate proliferation of cells of mesenchymal, epithelial and neuroectodermal origin. Additional members of the FGF family include the oncogenes FGF-3 (Int2) and FGF-4 (hst/Kaposi), FGF-5, FGF-6, FGF-7 (KGF), FGF-8 (AIGF), FGF-9 (GAF) and FGF-10 through FGF-23. Members of the FGF family share 30-55% amino acid sequence identity and similar gene structure, and are capable of transforming cultured cells when overexpressed in trans- fected cells. Cellular receptors for FGFs are members of a second multigene family, including four tyrosine kinases designated Flg (FGFR-1), Bek (FGFR-L), TKF and FGFR-3.
Lieferant:
Biotium
Beschreibung:
Cytochrome C is a well-characterized mobile electron transport protein that is essential to energy conversion in all aerobic organisms. In mammalian cells, this highly conserved protein is normally localized to the mitochondrial inter-membrane space. More recent studies have identified cytosolic cytochrome c as a factor necessary for activation of apoptosis. During apoptosis, cytochrome c is trans-located from the mitochondrial membrane to the cytosol, where it is required for activation of caspase-3 (CPP32). Overexpression of Bcl-2 has been shown to prevent the translocation of cytochrome c, thereby blocking the apoptotic process. Overexpression of Bax has been shown to induce the release of cytochrome c and to induce cell death. The release of cytochrome c from the mitochondria is thought to trigger an apoptotic cascade, whereby Apaf-1 binds to Apaf-3 (caspase-9) in a cytochrome c-dependent manner, leading to caspase-9 cleavage of caspase-3.
Artikel-Nr:
(BOSSBS-8333R-CY5.5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8333R-CY5.5
Lokale Artikelnummer::
BOSSBS-8333R-CY5.5
Beschreibung:
RDH13, also known as all-trans and 9-cis retinol dehydrogenase 13 or SDR7C3, is a 331 amino acid mitochondrial protein belonging to the short-chain dehydrogenases/reductases (SDR) family. Widely expressed, mostly in eye, pancreas, placenta and lung, RDH13 localizes on the outer side of the inner mitochondrial membrane. Related to microsomal retinoid oxidoreductase RDH11, RDH13 is considered to be a major enzyme among the RDH family of proteins. Catalytically active, RDH13 recognizes retinoids as substrates and may function in retinoic acid production. RDH13 may function to protect the mitochondria against oxidative stress. Leber congenital amaurosis (LCA) type 3, an inherited autosomal recessive retinal disease, has been associated with defects of RDH13. LCA represents the most common genetic cause of congenital visual impairment in infants and children.
VE:
1 * 100 µl
Lieferant:
Honeywell Chemicals
Beschreibung:
Decahydronaphthalin (Gemisch der cis- und trans-Isomeren) 98%, Reagenzqualität
Lieferant:
Biotium
Beschreibung:
Fibroblast growth factor-1 (FGF-1), also designated acidic FGF, and fibroblast growth factor-2 (FGF-2), also designated basic FGF, are members of a family of growth factors that stimulate proliferation of cells of mesenchymal, epithelial and neuroectodermal origin. Additional members of the FGF family include the oncogenes FGF-3 (Int2) and FGF-4 (hst/Kaposi), FGF-5, FGF-6, FGF-7 (KGF), FGF-8 (AIGF), FGF-9 (GAF) and FGF-10 through FGF-23. Members of the FGF family share 30-55% amino acid sequence identity and similar gene structure, and are capable of transforming cultured cells when overexpressed in trans- fected cells. Cellular receptors for FGFs are members of a second multigene family, including four tyrosine kinases designated Flg (FGFR-1), Bek (FGFR-L), TKF and FGFR-3.
Artikel-Nr:
(APOSOR9456-100MG)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR9456-100MG
Lokale Artikelnummer::
APOSOR9456-100MG
Beschreibung:
6-(Ethylsulphonyl)-2H-1,4-benzoxazin-3(4H)-one
VE:
1 * 100 mg
Preis auf Anfrage
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