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Bis(3-nitrophenyl)disulfid
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Bis(3-nitrophenyl)disulfid
Lieferant:
COMBI-BLOCKS
Beschreibung:
Ethyl-6-chlorimidazo[1,2-a]pyridin-2-carboxylat
Lieferant:
COMBI-BLOCKS
Beschreibung:
Methyl-3-bromimidazo[1,2-a]pyridin-6-carboxylat
Artikel-Nr:
(FLUO004737-25G)
Lieferant:
FLUOROCHEM
Hersteller-Artikelnummer::
004737-25G
Lokale Artikelnummer::
FLUO004737-25G
Beschreibung:
1,2-Dichlor-1,1,2-trifluor-2-iodethan
VE:
1 * 25 g
 This is a MarketSource item. Additional charges may apply
Artikel-Nr:
(24901-25MG)
Lieferant:
Sigma-Aldrich
Hersteller-Artikelnummer::
24901-25MG
Lokale Artikelnummer::
SUPL24901-25MG
Beschreibung:
Ionophore employed in solvent polymeric membrane electrodes for the assay of Cl- activity.
VE:
1 * 25 mg
Lieferant:
Sigma-Aldrich
Beschreibung:
1,2-Epoxy-5-hexen, Sigma-Aldrich®
Lieferant:
Sigma-Aldrich
Beschreibung:
(1S,2S)-(+)-trans-1,2-Cyclohexandiol, Sigma-Aldrich®
Artikel-Nr:
(BOSSBS-15130R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15130R-A555
Lokale Artikelnummer::
BOSSBS-15130R-A555
Beschreibung:
The smallest of the human chromosomes, 21 makes up about 1.5% of the human genome. Chromosome 21 contains nearly 300 genes and 47 million base pairs. Down syndrome, also known as trisomy 21, is the disease most commonly associated with chromosome 21. Alzheimer's disease, Jervell and Lange-Nielsen syndrome and amyotrophic lateral sclerosis are also associated with chromosome 21. Translocations are found to occur between chromosome 21 and 8, and chromosome 21 and 12, in certain leukemias. The C21orf88 gene product has been provisionally designated C21orf88 pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-15130R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15130R-CY7
Lokale Artikelnummer::
BOSSBS-15130R-CY7
Beschreibung:
The smallest of the human chromosomes, 21 makes up about 1.5% of the human genome. Chromosome 21 contains nearly 300 genes and 47 million base pairs. Down syndrome, also known as trisomy 21, is the disease most commonly associated with chromosome 21. Alzheimer's disease, Jervell and Lange-Nielsen syndrome and amyotrophic lateral sclerosis are also associated with chromosome 21. Translocations are found to occur between chromosome 21 and 8, and chromosome 21 and 12, in certain leukemias. The C21orf88 gene product has been provisionally designated C21orf88 pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11406R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11406R-HRP
Lokale Artikelnummer::
BOSSBS-11406R-HRP
Beschreibung:
GIOT-1 is a 563 amino acid protein belonging to the Krüppel C2H2-type zinc-finger protein family. Localized to the nucleus, GIOT-1 is widely expressed in tissues, with highest levels in liver, kidney, small intestine, pancreas and thymus. GIOT-1 contains 12 C2H2-type zinc fincers and one KRAB domain. Because the KRAB domain functions as a transcriptional repressor when attached to the template DNA, GIOT-1 is thought to be involved in transcriptional regulation. The gene encoding GIOT-1 is localized to chromosome 19q13.12 and two isoforms of GIOT-1 exist as a result of alternative splicing events.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-12919R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12919R-CY5
Lokale Artikelnummer::
BOSSBS-12919R-CY5
Beschreibung:
This gene is a member of the type II keratin family clustered on the long arm of chromosome 12. Type I and type II keratins heteropolymerize to form intermediate-sized filaments in the cytoplasm of epithelial cells. The product of this gene typically dimerizes with keratin 18 to form an intermediate filament in simple single-layered epithelial cells. This protein plays a role in maintaining cellular structural integrity and also functions in signal transduction and cellular differentiation. Mutations in this gene cause cryptogenic cirrhosis. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jan 2012].
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9975R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9975R-A750
Lokale Artikelnummer::
BOSSBS-9975R-A750
Beschreibung:
The smallest of the human chromosomes, 21 makes up about 1.5% of the human genome. Chromosome 21 contains nearly 300 genes and 47 million base pairs. Down syndrome, also known as trisomy 21, is the disease most commonly associated with chromosome 21. Alzheimer's disease, Jervell and Lange-Nielsen syndrome and amyotrophic lateral sclerosis are also associated with chromosome 21. Translocations are found to occur between chromosome 21 and 8, and chromosome 21 and 12, in certain leukaemias. The C21orf62 gene product has been provisionally designated C21orf62 pending further characterisation.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11406R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11406R-A350
Lokale Artikelnummer::
BOSSBS-11406R-A350
Beschreibung:
GIOT-1 is a 563 amino acid protein belonging to the Krüppel C2H2-type zinc-finger protein family. Localized to the nucleus, GIOT-1 is widely expressed in tissues, with highest levels in liver, kidney, small intestine, pancreas and thymus. GIOT-1 contains 12 C2H2-type zinc fincers and one KRAB domain. Because the KRAB domain functions as a transcriptional repressor when attached to the template DNA, GIOT-1 is thought to be involved in transcriptional regulation. The gene encoding GIOT-1 is localized to chromosome 19q13.12 and two isoforms of GIOT-1 exist as a result of alternative splicing events.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-12919R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12919R-FITC
Lokale Artikelnummer::
BOSSBS-12919R-FITC
Beschreibung:
This gene is a member of the type II keratin family clustered on the long arm of chromosome 12. Type I and type II keratins heteropolymerize to form intermediate-sized filaments in the cytoplasm of epithelial cells. The product of this gene typically dimerizes with keratin 18 to form an intermediate filament in simple single-layered epithelial cells. This protein plays a role in maintaining cellular structural integrity and also functions in signal transduction and cellular differentiation. Mutations in this gene cause cryptogenic cirrhosis. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jan 2012].
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-15130R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15130R-A647
Lokale Artikelnummer::
BOSSBS-15130R-A647
Beschreibung:
The smallest of the human chromosomes, 21 makes up about 1.5% of the human genome. Chromosome 21 contains nearly 300 genes and 47 million base pairs. Down syndrome, also known as trisomy 21, is the disease most commonly associated with chromosome 21. Alzheimer's disease, Jervell and Lange-Nielsen syndrome and amyotrophic lateral sclerosis are also associated with chromosome 21. Translocations are found to occur between chromosome 21 and 8, and chromosome 21 and 12, in certain leukemias. The C21orf88 gene product has been provisionally designated C21orf88 pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11406R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11406R-A555
Lokale Artikelnummer::
BOSSBS-11406R-A555
Beschreibung:
GIOT-1 is a 563 amino acid protein belonging to the Krüppel C2H2-type zinc-finger protein family. Localized to the nucleus, GIOT-1 is widely expressed in tissues, with highest levels in liver, kidney, small intestine, pancreas and thymus. GIOT-1 contains 12 C2H2-type zinc fincers and one KRAB domain. Because the KRAB domain functions as a transcriptional repressor when attached to the template DNA, GIOT-1 is thought to be involved in transcriptional regulation. The gene encoding GIOT-1 is localized to chromosome 19q13.12 and two isoforms of GIOT-1 exist as a result of alternative splicing events.
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.
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