Suche >
4\\\'-(Dimethylamino)biphenyl-3-carbonsäure
Drucken
Sie suchten nach:
26 347 results were found
4\\\'-(Dimethylamino)biphenyl-3-carbonsäure
Lieferant:
COMBI-BLOCKS
Beschreibung:
trans-3,4,4-Trimethyl-2-pentensäure
Artikel-Nr:
(FLUO019014-10G)
Lieferant:
FLUOROCHEM
Hersteller-Artikelnummer::
019014-10G
Lokale Artikelnummer::
FLUO019014-10G
Beschreibung:
2,4,6-Triisopropylbenzoesäure
VE:
1 * 10 g
 This is a MarketSource item. Additional charges may apply
Artikel-Nr:
(COBBBB-5913-1G)
Lieferant:
COMBI-BLOCKS
Hersteller-Artikelnummer::
BB-5913-1G
Lokale Artikelnummer::
COBBBB-5913-1G
Beschreibung:
4-(trans-4-Propylcyclohexyl)phenylboronsäure
VE:
1 * 1 g
This is a MarketSource item. Additional charges may apply
Artikel-Nr:
(32615-100G)
Lieferant:
Honeywell Chemicals
Hersteller-Artikelnummer::
32615-100G
Lokale Artikelnummer::
HONC32615-100G
Beschreibung:
Fluorescein freie Säure Reag. Ph. Eur., Fluka™
VE:
1 * 100 g
Artikel-Nr:
(BOSSBS-8333R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8333R-A750
Lokale Artikelnummer::
BOSSBS-8333R-A750
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 localises 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 recognises 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
Artikel-Nr:
(BOSSBS-8333R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8333R-HRP
Lokale Artikelnummer::
BOSSBS-8333R-HRP
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:
APOLLO SCIENTIFIC
Beschreibung:
1-(4-Bromo-1-cyclopropyl-1H-pyrazol-3-yl)methanamine dihydrochloride 95%
Lieferant:
COMBI-BLOCKS
Beschreibung:
4-(trans-2-Carboxyvinyl)phenylboronsäure
Lieferant:
MP Biomedicals
Beschreibung:
<i>p</i>-Coumaric acid is a hydroxycinnamic acid, an organic compound that is a hydroxy derivative of cinnamic acid. There are three isomers of coumaric acid- <i>o</i>-coumaric acid, <i>m</i>-coumaric acid, and <i>p</i>-coumaric acid- that differ by the position of the hydroxy substitution of the phenyl group.
Lieferant:
Sigma-Aldrich
Beschreibung:
4-Acetylbenzoesäure, Sigma-Aldrich®
Artikel-Nr:
(SIAL513490-5G)
Lieferant:
Sigma-Aldrich
Hersteller-Artikelnummer::
513490-5G
Lokale Artikelnummer::
SIAL513490-5G
Beschreibung:
4-Carboxyphenylboronsäurepinakolester, Sigma-Aldrich®
VE:
1 * 5 g
Artikel-Nr:
(BOSSBS-13487R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13487R-CY7
Lokale Artikelnummer::
BOSSBS-13487R-CY7
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 Sjé°ƒren's syndrome and Hepatitis B.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13487R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13487R-A350
Lokale Artikelnummer::
BOSSBS-13487R-A350
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 Sjé°ƒren's syndrome and Hepatitis B.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11785R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11785R-A647
Lokale Artikelnummer::
BOSSBS-11785R-A647
Beschreibung:
Maspardin is a 308 amino acid cytoplasmic protein that is widely expressed. Belonging to the AB hydrolase superfamily, Maspardin colocalizes with CD4 on endosomal/trans-Golgi network. It is thought that Maspardin may act as a negative regulatory factor in CD4-dependent T-cell activation. Defects in the gene encoding Maspardin are the result of hereditary spastic paraplegia autosomal recessive type 21 (also designated Mast syndrome), an autosomal recessive neurodegenerative disorder characterized by a slow, gradual, progressive weakness and spasticity of the lower limbs. The gene encoding Maspardin is encoded by human chromosome 15, which houses over 700 genes and comprises nearly 3% of the human genome.
VE:
1 * 100 µl
Lieferant:
FLUOROCHEM
Beschreibung:
trans-3,3-Dimethyl-1-butenylboronsäure
Lieferant:
COMBI-BLOCKS
Beschreibung:
trans-4-Aminocyclohexancarbonsäure Hydrochlorid
Preis auf Anfrage
Lager für diesen Artikel ist begrenzt, kann aber in einem Lagerhaus in Ihrer Nähe zur Verfügung. Bitte stellen Sie sicher, dass Sie in sind angemeldet auf dieser Seite, so dass verfügbare Bestand angezeigt werden können. Wenn das
 noch angezeigt wird und Sie Hilfe benötigen, rufen Sie uns an 1-800-932 - 5000.
Lager für diesen Artikel ist begrenzt, kann aber in einem Lagerhaus in Ihrer Nähe zur Verfügung. Bitte stellen Sie sicher, dass Sie in sind angemeldet auf dieser Seite, so dass verfügbare Bestand angezeigt werden können. Wenn das
noch angezeigt wird und Sie Hilfe benötigen, rufen Sie uns an 1-800-932 - 5000.
Dieses Produkt kann nur an eine Lieferadresse versandt werden die über die entsprechende Lizenzen verfügt. Für weitere Hilfe bitte kontaktieren Sie Ihr VWR Vertriebszentrum.
-Additional Documentation May be needed to purchase this item. A VWR representative will contact you if needed.
Dieses Produkt wurde von Ihrer Organisation gesperrt. Bitte kontaktieren Sie Ihren Einkauf für weitere Informationen.
Dieses Produkt ist Ersatz für den von Ihnen gewünschten Artikel.
Dieses Produkt ist nicht mehr verfügbar. Bitte kontaktieren Sie den VWR Kundenservice.
|
|||||||||
Listenansicht
