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17-Octadecins\\\\\\\\u00E4ure
Lieferant:
Molekula
Beschreibung:
7-Amino-4-methylcumarin
Artikel-Nr:
(BOSSBS-11825R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11825R-A680
Lokale Artikelnummer::
BOSSBS-11825R-A680
Beschreibung:
DOCK 7 is a 2140 amino acid protein that localizes to developing axons and contains one DHR-1 domain and one DHR-2 domain. Expressed in a variety of tissues, DOCK 7 functions as a guanine nucleotide exchange factor (GEF) that specifically activates Rac 1 and Rac 3 by catalyzing the exchange of bound GDP for free GTP. Multiple isoforms of DOCK 7 exist due to alternative splicing events.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-0136R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-0136R-A750
Lokale Artikelnummer::
BOSSBS-0136R-A750
Beschreibung:
GTP cyclohydrolase I (also designated dopa-responsive dystonia) catalyses the conversion of GTP to D-erythro-7,8-dihydroneopterin triphosphate, the first and rate-limiting step in tetrahydrobiopterin (BH4) biosynthesis. Tetrahydrobiopterin is an essential cofactor for 3 aromatic amino acid monooxygenases: phenylalanine, tyrosine, and tryptophan hydroxylases. Animals can synthesise tetrahydrobiopterin in vivo from GTP through several enzymatic reactions.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11825R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11825R-A750
Lokale Artikelnummer::
BOSSBS-11825R-A750
Beschreibung:
DOCK 7 is a 2140 amino acid protein that localizes to developing axons and contains one DHR-1 domain and one DHR-2 domain. Expressed in a variety of tissues, DOCK 7 functions as a guanine nucleotide exchange factor (GEF) that specifically activates Rac 1 and Rac 3 by catalyzing the exchange of bound GDP for free GTP. Multiple isoforms of DOCK 7 exist due to alternative splicing events.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11825R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11825R-HRP
Lokale Artikelnummer::
BOSSBS-11825R-HRP
Beschreibung:
DOCK 7 is a 2,140 amino acid protein that localizes to developing axons and contains one DHR-1 domain and one DHR-2 domain. Expressed in a variety of tissues, DOCK 7 functions as a guanine nucleotide exchange factor (GEF) that specifically activates Rac 1 and Rac 3 by catalyzing the exchange of bound GDP for free GTP. Multiple isoforms of DOCK 7 exist due to alternative splicing events.
VE:
1 * 100 µl
Artikel-Nr:
(SIAL642770-5G)
Lieferant:
Sigma-Aldrich
Hersteller-Artikelnummer::
642770-5G
Lokale Artikelnummer::
SIAL642770-5G
Beschreibung:
4-Amino-3-brombenzonitril, Sigma-Aldrich®
VE:
1 * 5 g
Artikel-Nr:
(EHERC10280000)
Lieferant:
EHRENSTORFER
Hersteller-Artikelnummer::
C10280000
Lokale Artikelnummer::
EHERC10280000
Beschreibung:
2-Amino-N-isopropylbenzamid
VE:
1 * 0,1 g
Lieferant:
FLUOROCHEM
Beschreibung:
2-Amino-6-methylpyridin
Lieferant:
Thermo Scientific
Beschreibung:
3-Amino-p-toluylsäure
Artikel-Nr:
(EHERC10225000)
Lieferant:
EHRENSTORFER
Hersteller-Artikelnummer::
C10225000
Lokale Artikelnummer::
EHERC10225000
Beschreibung:
4-Amino-2-methylchinolin
VE:
1 * 0,1 g
Artikel-Nr:
(MOLEM43883839)
Lieferant:
Molekula
Hersteller-Artikelnummer::
M43883839
Lokale Artikelnummer::
MOLEM43883839
Beschreibung:
2-Amino-6-brompyridin
VE:
1 * 5 g
 This is a MarketSource item. Additional charges may apply
Artikel-Nr:
(FLUO015547-1G)
Lieferant:
FLUOROCHEM
Hersteller-Artikelnummer::
015547-1G
Lokale Artikelnummer::
FLUO015547-1G
Beschreibung:
8-Amino-5-bromchinolin
VE:
1 * 1 g
This is a MarketSource item. Additional charges may apply
Lieferant:
FLUOROCHEM
Beschreibung:
2-Amino-6-fluorpyridin
Artikel-Nr:
(BOSSBS-13138R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13138R-FITC
Lokale Artikelnummer::
BOSSBS-13138R-FITC
Beschreibung:
Fanconi anemia (FA) is an autosomal recessive disorder characterized by bone marrow failure, birth defects and chromosomal instability. At the cellular level, FA is characterized by spontaneous chromosomal breakage and a unique hypersensitivity to DNA cross-linking agents. At least eight complementation groups (A-G) have been identified and six FA genes (for subtypes A, C, D2, E, F and G) have been cloned. The FA proteins lack sequence homologies or motifs that could point to a molecular function. The cellular accumulation of FA proteins, including FANCA and FANCG, is subject to regulation by TNF alpha signaling. Phosphorylation of FANC (Fanconi anemia complementation group) proteins is thought to be important for the function of the FA pathway. FANCA, also known as FACA and FANCH, associates with the Brm-related gene 1 (BRG1) product, a subunit of the SWI/SNF complex which remodels chromatin structure through a DNA-dependent ATPase activity. FANCA is mainly expressed in lymphoid tissues, testis and ovary. The amino-terminal region of the FANCA protein is required for FANCG binding, FANCC binding, nuclear localization and functional activity of the complex. The human FANCA gene maps to chromosome 16q24.3 and encodes a 1,455 amino acid protein.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13138R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13138R-A488
Lokale Artikelnummer::
BOSSBS-13138R-A488
Beschreibung:
Fanconi anemia (FA) is an autosomal recessive disorder characterized by bone marrow failure, birth defects and chromosomal instability. At the cellular level, FA is characterized by spontaneous chromosomal breakage and a unique hypersensitivity to DNA cross-linking agents. At least eight complementation groups (A-G) have been identified and six FA genes (for subtypes A, C, D2, E, F and G) have been cloned. The FA proteins lack sequence homologies or motifs that could point to a molecular function. The cellular accumulation of FA proteins, including FANCA and FANCG, is subject to regulation by TNF alpha signaling. Phosphorylation of FANC (Fanconi anemia complementation group) proteins is thought to be important for the function of the FA pathway. FANCA, also known as FACA and FANCH, associates with the Brm-related gene 1 (BRG1) product, a subunit of the SWI/SNF complex which remodels chromatin structure through a DNA-dependent ATPase activity. FANCA is mainly expressed in lymphoid tissues, testis and ovary. The amino-terminal region of the FANCA protein is required for FANCG binding, FANCC binding, nuclear localization and functional activity of the complex. The human FANCA gene maps to chromosome 16q24.3 and encodes a 1,455 amino acid protein.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11959R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11959R-A750
Lokale Artikelnummer::
BOSSBS-11959R-A750
Beschreibung:
The leucine-rich (LRR) repeat is a 20 to 30 amino acid motif that forms a hydrophobic å/ horseshoe fold, allowing it to accommodate several leucine residues within a tightly packed core. All LRR repeats contain a variable segment and a highly conserved segment, the latter of which accounts for 11 or 12 residues of the entire LRR motif. SLITRK5 (SLIT and NTRK-like family, member 5), also known as LRRC11 (leucine-rich repeat-containing protein 11), is a 958 amino acid single-pass type I membrane protein that contains 16 LRR repeats and belongs to the SLITRK family. Expressed at high levels in the cerebral cortex, but also present in areas of the spinal cord and medulla, SLITRK5 functions to suppress neurite outgrowth, thereby playing a regulatory role in neuronal function. The gene encoding SLITRK5 maps to human chromosome 13, which houses over 400 genes, such as BRCA2 and RB1, and comprises nearly 4% of the human genome. Trisomy 13, also known as Patau syndrome, is deadly and the few who survive past one year suffer from permanent neurologic defects, difficulty eating and vulnerability to serious respiratory infections.
VE:
1 * 100 µl
Preis auf Anfrage
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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.
Dieses Produkt kann nur an eine Lieferadresse versandt werden die über die entsprechende Lizenzen verfügt. Für weitere Hilfe bitte kontaktieren Sie Ihr VWR Vertriebszentrum.
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