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3,5-Diiodsalicyls\\\\u00E4ure
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3,5-Diiodsalicyls\\\\u00E4ure
Artikel-Nr:
(BOSSBS-11797R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11797R-A488
Lokale Artikelnummer::
BOSSBS-11797R-A488
Beschreibung:
Aldehyde dehydrogenases (ALDHs) mediate the NADP+-dependent oxidation of aldehydes into acids and play an important role in the detoxification of alcohol-derived acetaldehyde, as well as in lipid peroxidation and in the metabolism of corticosteroids, biogenic amines and neurotransmitters. ALDH3A2 (aldehyde dehydrogenase 3 family, member A2), also known as SLS, FALDH or ALDH10, is a 485 amino acid single-pass membrane protein that localizes to the cytoplasmic side of the endoplasmic reticulum and belongs to the aldehyde dehydrogenase family. Expressed in a variety of tissues, including liver, heart, lung, brain, kidney and placenta, ALDH3A2 catalyzes the NAD+-dependent oxidation of long-chain aliphatic aldehydes to fatty acids, a process that is necessary for detoxification and lipid metabolism. Defects in the gene encoding ALDH3A2 are the cause of Sjoegren-Larsson syndrome (SLS), an autosomal recessive neurocutaneous disorder characterized by severe mental retardation, seizures and speech defects. Multiple isoforms of ALDH3A2 exist due to alternative splicing events.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-12096R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12096R-CY5
Lokale Artikelnummer::
BOSSBS-12096R-CY5
Beschreibung:
Peroxisomes are single-membrane bound organelles present in virtually all eukaryotic cells. They are involved in numerous catabolic and anabolic pathways, including beta-oxidation of very long chain fatty acids, metabolism of hydrogen peroxide, plasmalogen biosynthesis and bile acid synthesis. The Peroxin gene family, which includes more than 20 members, is required for peroxisome biogenesis. Peroxin 5R, also known as PEX5-related protein or Peroxisome biogenesis factor 5-like, is a 626 amino acid protein that is mainly expressed in brain, with some expression in testis and pancreas. Peroxin 5R contains five TPR repeats, which enable protein-protein interactions and assembly of large multiprotein complexes. There are three isoforms of Peroxin 5R that are produced as a result of alternative splicing events. These isoforms bind C-terminal peroxisome-targeting signals in a similar manner to Peroxin-5. Peroxin 5R interacts with Rab 8b, possibly playing a role in vesicular trafficking and neurotransmitter release.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-5862R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5862R-A680
Lokale Artikelnummer::
BOSSBS-5862R-A680
Beschreibung:
ADAMTS (A Disintegrin And Metalloproteinase Domain with Thrombospondin type 1 Modules) is a family of zinc-dependent proteases that are implicated in a variety of normal and pathological conditions, including arthritis and cancer. ADAMTS protein family members contain an amino-terminal propeptide domain, a metalloproteinase domain, a disintegrin-like domain and a carboxy-terminus that contains a varying number of Thrombospondin type 1 (TSP-1) motifs. ADAMTS-L2 (ADAMTS-like protein 2) is a 951 amino acid secreted protein that is highly expressed in lung, kidney and liver. Mutations in the gene encoding ADAMTS are the cause of geleophysic dysplasia, an autosomal recessive disorder characterised by cardiac vavular anomalies, short stature, thick skin and brachydactyly. In individuals affected with geleophysic dysplasia, there is a significant increase in total active TGF-beta 1 and nuclear locations of p-SAMD2 in fibroblasts. Interestingly, ADAMTS-L2 interacts with LTBP-1, a glycoprotein that is part of the platelet-derived TGF-beta 1 complex.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-5862R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5862R-A647
Lokale Artikelnummer::
BOSSBS-5862R-A647
Beschreibung:
ADAMTS (A Disintegrin And Metalloproteinase Domain with Thrombospondin type 1 Modules) is a family of zinc-dependent proteases that are implicated in a variety of normal and pathological conditions, including arthritis and cancer. ADAMTS protein family members contain an amino-terminal propeptide domain, a metalloproteinase domain, a disintegrin-like domain and a carboxy-terminus that contains a varying number of Thrombospondin type 1 (TSP-1) motifs. ADAMTS-L2 (ADAMTS-like protein 2) is a 951 amino acid secreted protein that is highly expressed in lung, kidney and liver. Mutations in the gene encoding ADAMTS are the cause of geleophysic dysplasia, an autosomal recessive disorder characterized by cardiac vavular anomalies, short stature, thick skin and brachydactyly. In individuals affected with geleophysic dysplasia, there is a significant increase in total active TGF-beta 1 and nuclear locations of p-SAMD2 in fibroblasts. Interestingly, ADAMTS-L2 interacts with LTBP-1, a glycoprotein that is part of the platelet-derived TGF-beta 1 complex.
VE:
1 * 100 µl
Lieferant:
COMBI-BLOCKS
Beschreibung:
3-Amino-2-naphthoesäure
Artikel-Nr:
(COBBBB-8526-1G)
Lieferant:
COMBI-BLOCKS
Hersteller-Artikelnummer::
BB-8526-1G
Lokale Artikelnummer::
COBBBB-8526-1G
Beschreibung:
4-Amino-3-nitrophenylboronsäure
VE:
1 * 1 g
 This is a MarketSource item. Additional charges may apply
Artikel-Nr:
(SIAL691429-5G)
Lieferant:
Sigma-Aldrich
Hersteller-Artikelnummer::
691429-5G
Lokale Artikelnummer::
SIAL691429-5G
Beschreibung:
3-Amino-o-anissäure, Sigma-Aldrich®
VE:
1 * 5 g
Lieferant:
BIONET RESEARCH
Beschreibung:
3-Amino-3-(3-bromphenyl)propionsäure
Artikel-Nr:
(COBBBB-2008-1G)
Lieferant:
COMBI-BLOCKS
Hersteller-Artikelnummer::
BB-2008-1G
Lokale Artikelnummer::
COBBBB-2008-1G
Beschreibung:
3-Amino-5-nitrophenylboronsäure Hydrochlorid
VE:
1 * 1 g
This is a MarketSource item. Additional charges may apply
Lieferant:
BIONET RESEARCH
Beschreibung:
3-Amino-3-(4-chlorphenyl)propionsäure
Artikel-Nr:
(SIAL21625-1G)
Lieferant:
Sigma-Aldrich
Hersteller-Artikelnummer::
21625-1G
Lokale Artikelnummer::
SIAL21625-1G
Beschreibung:
3-Amino-5-methylcapronsäure, Sigma-Aldrich®
VE:
1 * 1 g
Artikel-Nr:
(BOSSBS-11797R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11797R-A750
Lokale Artikelnummer::
BOSSBS-11797R-A750
Beschreibung:
Aldehyde dehydrogenases (ALDHs) mediate the NADP+-dependent oxidation of aldehydes into acids and play an important role in the detoxification of alcohol-derived acetaldehyde, as well as in lipid peroxidation and in the metabolism of corticosteroids, biogenic amines and neurotransmitters. ALDH3A2 (aldehyde dehydrogenase 3 family, member A2), also known as SLS, FALDH or ALDH10, is a 485 amino acid single-pass membrane protein that localizes to the cytoplasmic side of the endoplasmic reticulum and belongs to the aldehyde dehydrogenase family. Expressed in a variety of tissues, including liver, heart, lung, brain, kidney and placenta, ALDH3A2 catalyses the NAD+-dependent oxidation of long-chain aliphatic aldehydes to fatty acids, a process that is necessary for detoxification and lipid metabolism. Defects in the gene encoding ALDH3A2 are the cause of Sjoegren-Larsson syndrome (SLS), an autosomal recessive neurocutaneous disorder characterised by severe mental retardation, seizures and speech defects. Multiple isoforms of ALDH3A2 exist due to alternative splicing events.
VE:
1 * 100 µl
Artikel-Nr:
(COBBPN-8671-1G)
Lieferant:
COMBI-BLOCKS
Hersteller-Artikelnummer::
PN-8671-1G
Lokale Artikelnummer::
COBBPN-8671-1G
Beschreibung:
4-Amino-3-methoxyphenylboronsäurepinakolester
VE:
1 * 1 g
This is a MarketSource item. Additional charges may apply
Lieferant:
COMBI-BLOCKS
Beschreibung:
2-Amino-5-chlorphenylboronsäurepinakolester
Artikel-Nr:
(BLDPBD123151-500G)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD123151-500G
Lokale Artikelnummer::
BLDPBD123151-500G
Beschreibung:
Cysteaminiumchlorid 98%
VE:
1 * 500 g
Lieferant:
COMBI-BLOCKS
Beschreibung:
3-Amino-4-chlorphenylboronsäurepinakolester
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 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.
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