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Tris(pentafluorphenyl)boran
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
Biphenyl-4,4'-dicarbonsäure
Artikel-Nr:
(BOSSBS-9102R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9102R-A680
Lokale Artikelnummer::
BOSSBS-9102R-A680
Beschreibung:
Belongs to the sulfatase family. Sulfatases such as ARSK, hydrolyze sulfate esters from sulfated steroids,carbohydrates, proteoglycans, and glycolipids. They are involved in hormone biosynthesis, modulation of cell signaling, and degradation of macromolecules.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-12479R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12479R-A750
Lokale Artikelnummer::
BOSSBS-12479R-A750
Beschreibung:
TMEM16C is a 981 amino acid multi-pass membrane protein that is encoded by a gene which maps to chromosome 11. With approximately 135 million base pairs and 1400 genes, chromosome 11 makes up around 4% of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and thalassemia are caused by HBB gene mutations, while Wilms' tumours, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-12068R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12068R-A680
Lokale Artikelnummer::
BOSSBS-12068R-A680
Beschreibung:
TMEM132A is a 560 amino acid protein encoded by a gene mapping to human chromosome 11. With approximately 135 million base pairs and 1400 genes, chromosome 11 makes up around 4% of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and thalassemia are caused by HBB gene mutations. Wilms' tumours, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9935R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9935R-A680
Lokale Artikelnummer::
BOSSBS-9935R-A680
Beschreibung:
C11orf16 is a 404 amino acid protein that is encoded by a gene located on human chromosome 11. With approximately 135 million base pairs and 1400 genes, chromosome 11 makes up around 4% of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and _ thalassemia are caused by HBB gene mutations. Wilms' tumours, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-12068R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12068R-FITC
Lokale Artikelnummer::
BOSSBS-12068R-FITC
Beschreibung:
TMEM132A is a 560 amino acid protein encoded by a gene mapping to human chromosome 11. With approximately 135 million base pairs and 1,400 genes, chromosome 11 makes up around 4% of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and ∫ thalassemia are caused by HBB gene mutations. Wilms' tumors, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-12068R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12068R-A488
Lokale Artikelnummer::
BOSSBS-12068R-A488
Beschreibung:
TMEM132A is a 560 amino acid protein encoded by a gene mapping to human chromosome 11. With approximately 135 million base pairs and 1,400 genes, chromosome 11 makes up around 4% of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and ∫ thalassemia are caused by HBB gene mutations. Wilms' tumors, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11.
VE:
1 * 100 µl
Artikel-Nr:
(83544.180)
Lieferant:
VWR Chemicals
Lokale Artikelnummer::
VWRC83544.180
Beschreibung:
Phenolphthalein 98,0-101,0% Ph. Eur.
VE:
1 * 100 g
Artikel-Nr:
(APOSPC8027-1G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
PC8027-1G
Lokale Artikelnummer::
APOSPC8027-1G
Beschreibung:
4-(2-Bromo-5-fluorobenzoyl)morpholine
VE:
1 * 1 g
Artikel-Nr:
(APOSOR471453-5G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR471453-5G
Lokale Artikelnummer::
APOSOR471453-5G
Beschreibung:
4'-Brom-N,N-diphenyl-4-biphenylamin
VE:
1 * 5 g
Artikel-Nr:
(BOSSBS-9102R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9102R-A350
Lokale Artikelnummer::
BOSSBS-9102R-A350
Beschreibung:
Belongs to the sulfatase family. Sulfatases such as ARSK, hydrolyze sulfate esters from sulfated steroids,carbohydrates, proteoglycans, and glycolipids. They are involved in hormone biosynthesis, modulation of cell signaling, and degradation of macromolecules.
VE:
1 * 100 µl
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
Kartogenin
Lieferant:
Alfa Aesar
Beschreibung:
4'-(4-Bromphenyl)acetophenon ≥97%
Artikel-Nr:
(MFLX70725-11)
Lieferant:
Avantor Fluid Handling
Hersteller-Artikelnummer::
70725-11
Lokale Artikelnummer::
MFLB70725-11
Beschreibung:
Robuster Dauerbetrieb mit Chemikalien- und Korrosionsbeständigkeit.
VE:
1 * 1 ST
Lieferant:
Thermo Scientific
Beschreibung:
3-Hydroxyphenylacetylene 95+%
Artikel-Nr:
(BLDPBD98621-5G)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD98621-5G
Lokale Artikelnummer::
BLDPBD98621-5G
Beschreibung:
4-Methoxypyridazine 98%
VE:
1 * 5 g
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.
-Additional Documentation May be needed to purchase this item. A VWR representative will contact you if needed.
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Dieses Produkt ist Ersatz für den von Ihnen gewünschten Artikel.
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