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Ethyl+3-(2-aminophenyl)acrylate
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Ethyl+3-(2-aminophenyl)acrylate
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
Carnosolsäure freie Säure ≥99%
Lieferant:
Merck
Beschreibung:
Ziehl-Neelsen carbolfuchsin solution - for microscopy, is a ready-to use solution used in the Ziehl-Neelsen hot staining for the microscopic investigation of acid-fast bacteria(AFB).
Artikel-Nr:
(BOSSBS-9659R-CY5.5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9659R-CY5.5
Lokale Artikelnummer::
BOSSBS-9659R-CY5.5
Beschreibung:
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 β 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. The FAM76B gene product has been provisionally designated FAM76B pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11888R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11888R-A555
Lokale Artikelnummer::
BOSSBS-11888R-A555
Beschreibung:
MPPED2 (Metallophosphoesterase domain-containing protein 2), also known as C11orf8, FAM1B or 239FB, is a 294 amino acid protein. Expressed primarily in fetal brain tissue, MPPED2 is encoded by a gene that maps to 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 stranded 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' 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
Lieferant:
SGE Analytical Science
Beschreibung:
Endura-Seals are the CRS alternative to typical silicone-rubber injection port septa for gas chromatography. They work in a 2 part sealing system that includes the septa and the sealing nut.
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
4-Fluor-3-nitrotoluol 99%
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
2-Brom-4-methoxyphenol
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
2-Chloro-3-hydroxybenzonitrile 95%
Artikel-Nr:
(1372333.)
Lieferant:
USP
Hersteller-Artikelnummer::
1372333
Lokale Artikelnummer::
USPH1372333
Beschreibung:
USP Reference Standards are specified for use in conducting official USP–NF tests and assays. USP also provides Reference Standards specified in the Food Chemicals Codex as well as authentic substances—high-quality chemical samples—as a service to analytical, clinical, pharmaceutical and research laboratories. To confirm accuracy and reproducibility, USP Reference Standards are rigorously tested and evaluated by multiple independent laboratories including USP, commercial, regulatory, and academic labs. USP also provide publicly available, official documentary standards for pharmaceutical ingredients in the USP–NF that link directly with our primary reference standards.
VE:
1 * 200 mg
Artikel-Nr:
(APOSOR5402-5G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR5402-5G
Lokale Artikelnummer::
APOSOR5402-5G
Beschreibung:
(S)-Methyl N-tert-butoxycarbonyl-3-(4-biphenylyl)-2-aminopropionate 98%
VE:
1 * 5 g
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
1H,1H-Perfluorohexan-1-ol 98%
Artikel-Nr:
(BLDPBD18381-5G)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD18381-5G
Lokale Artikelnummer::
BLDPBD18381-5G
Beschreibung:
Candesartancilexetil 98%
VE:
1 * 5 g
Artikel-Nr:
(BOSSBS-12068R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12068R-A350
Lokale Artikelnummer::
BOSSBS-12068R-A350
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-9935R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9935R-A750
Lokale Artikelnummer::
BOSSBS-9935R-A750
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:
(AGLS200209)
Lieferant:
AGILENT
Hersteller-Artikelnummer::
200209
Lokale Artikelnummer::
AGLS200209
Beschreibung:
For libraries constructed from highly methylated DNA, Gigapack III Packaging Extract simplifies the packaging procedure and increases the efficiency and representation of libraries constructed from highly methylated DNA. Each packaging extract is restriction minus to optimize packaging efficiency and library representation.
VE:
1 * 1 ST
Artikel-Nr:
(BLDPBD237991-1G)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD237991-1G
Lokale Artikelnummer::
BLDPBD237991-1G
Beschreibung:
2-Chloro-3-hydroxybenzonitrile 97%
VE:
1 * 1 g
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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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