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Methyl+indoline-5-carboxylate
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Methyl+indoline-5-carboxylate
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
2-Ethynylpyrazine 98%
Artikel-Nr:
(APOSOR314002-1G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR314002-1G
Lokale Artikelnummer::
APOSOR314002-1G
Beschreibung:
2-(4-Chlorophenyl)-2',4'-dichloroacetophenone
VE:
1 * 1 g
Artikel-Nr:
(BOSSBS-12479R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12479R-CY3
Lokale Artikelnummer::
BOSSBS-12479R-CY3
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 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, 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
Artikel-Nr:
(BOSSBS-12068R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12068R-CY5
Lokale Artikelnummer::
BOSSBS-12068R-CY5
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-9940R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9940R-A680
Lokale Artikelnummer::
BOSSBS-9940R-A680
Beschreibung:
C11orf65, also known as MGC33948, is a 313 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
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
4-Fluor-3-nitrotoluol 99%
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
2-Fluoro-4-(methylsulphonyl)benzaldehyde
Artikel-Nr:
(1554705.)
Lieferant:
USP
Hersteller-Artikelnummer::
1554705
Lokale Artikelnummer::
USPH1554705
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 * 350 mg
Artikel-Nr:
(EBRO1340-6265)
Lieferant:
EBRO
Hersteller-Artikelnummer::
1340-6265
Lokale Artikelnummer::
EBRO1340-6265
Beschreibung:
The EBI 11-TP210 temperature and pressure data logger is designed for routine checks in the food and pharmaceutical industries, focusing on canning factories. It offers precise pasteurisation control with a measuring range of 1 to 8000 mbar and 0 to +140 °C. Its small size allows for easy placement in tight spaces, while the autoclave-proof, IP 68 housing ensures durability and reliability, making it ideal for food safety.
VE:
1 * 1 ST
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
2-Brom-4-methoxyphenol
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
2-Chloro-3-hydroxybenzonitrile 95%
Lieferant:
ANSELL HEALTH CARE
Beschreibung:
Durable, touchscreen-compatible gloves that guard against electrostatic discharge.
Lieferant:
SIGMA ALDRICH MICROSCOPY
Beschreibung:
Azure A is a basic cationic dye. The combination of azure A and silver staining is used for the quantification of glycosaminoglycans in agarose gels. It is also used for the staining of chromosomes in the nucleus. It is a main component of the azure B/polychromed methylene blue – eosin stains family, also referred to as the Romanowsky stain.
Lieferant:
Thermo Scientific
Beschreibung:
Morpholin-3-on 98%
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
3,5-Difluor-4-methoxybenzaldehyd
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
4-Acetamido-3-fluorobenzoic acid 97%
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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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