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5-Oxaspiro[3.5]nonan-8-one
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5-Oxaspiro[3.5]nonan-8-one
Artikel-Nr:
(BOSSBS-9617R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9617R-HRP
Lokale Artikelnummer::
BOSSBS-9617R-HRP
Beschreibung:
C14orf174, is a 674 amino acid protein that contains one SAM (sterile alpha motif) domain. Existing as two alternatively spliced isoforms,C14orf174 is encoded by a gene that maps to human chromosome 14q24.3. Chromosome 14 contains about 700 genes and 106 million base pairs and makes up about 3.5% of human cellular DNA. Chromosome 14 encodes the presinilin 1 (PSEN1) gene, which is one of the three key genes associated with the development of Alzheimer's disease. The SERPINA1 gene is located on chromosome 14 and when defective leads to the genetic disorder ?-antitrypsin deficiency. This disorder is characterized by severe lung complications and liver dysfunction. Notably, the immunoglobulin heavy chain locus is found on chromosome 14 and has been identified as a fusion with the chromosome 19 encoded protein Bcl-3 in the (14;19) translocations found in a variety of B cell malignancies.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-2675R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-2675R-A647
Lokale Artikelnummer::
BOSSBS-2675R-A647
Beschreibung:
a-Fodrin is a universally expressed membrane associated cytoskeletal protein consisting of alpha and beta subunits. The protein is important for maintaining normal membrane structure and supporting cell surface protein function. Alpha Fodrin is one of the important targets cleaved by caspases during apoptosis. The full length 240 kDa protein can be cleaved at several sites within its sequence by activated caspases generating N terminal 150 kDa, C terminal 120 kDa, and 35 kDa major products. Cleavage of alpha Fodrin leads to membrane malfunction and cell shrinkage.
VE:
1 * 100 µl
Lieferant:
Thermo Scientific
Beschreibung:
1,9-Nonandiol 99%
Artikel-Nr:
(APOSOR471010-1G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR471010-1G
Lokale Artikelnummer::
APOSOR471010-1G
Beschreibung:
4,6-Nonandion
VE:
1 * 1 g
Artikel-Nr:
(BOSSBS-8226R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8226R-CY5
Lokale Artikelnummer::
BOSSBS-8226R-CY5
Beschreibung:
FAM161B is a 647 amino acid protein that belongs to the FAM161 family. The gene that encodes FAM161B consists of approximately 16,413 bases and maps to human chromosome 14q24.3. Housing over 700 genes, chromosome 14 comprises nearly 3.5% of the human genome. Chromosome 14 encodes the Presenilin 1 (PSEN1) gene, which is one of the three key genes associated with the development of Alzheimer’s disease. The SERPINA1 gene is also located on chromosome 14 and, when defective, leads to the genetic disorder α1-antitrypsin deficiency, which is characterized by severe lung complications and liver dysfunction. An inversion of the long arm of chromosome 14 is thought to be involved in T-cell chronic lymphocytic leukemia (CLL), a cancer that affects T lymphocytes.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8226R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8226R-A647
Lokale Artikelnummer::
BOSSBS-8226R-A647
Beschreibung:
FAM161B is a 647 amino acid protein that belongs to the FAM161 family. The gene that encodes FAM161B consists of approximately 16,413 bases and maps to human chromosome 14q24.3. Housing over 700 genes, chromosome 14 comprises nearly 3.5% of the human genome. Chromosome 14 encodes the Presenilin 1 (PSEN1) gene, which is one of the three key genes associated with the development of Alzheimer’s disease. The SERPINA1 gene is also located on chromosome 14 and, when defective, leads to the genetic disorder α1-antitrypsin deficiency, which is characterized by severe lung complications and liver dysfunction. An inversion of the long arm of chromosome 14 is thought to be involved in T-cell chronic lymphocytic leukemia (CLL), a cancer that affects T lymphocytes.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8260R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8260R-CY3
Lokale Artikelnummer::
BOSSBS-8260R-CY3
Beschreibung:
DHRS1 (dehydrogenase/reductase (SDR family) member 1), also known as SDR19C1, is a 313 amino acid protein that belongs to the short-chain dehydrogenases/reductases (SDR) family and likely functions as an oxidoreductase. Abundantly expressed in heart and liver, DHRS1 contains an SDR motif and is encoded by a gene that maps to human chromosome 14q12. Human chromosome 14 houses over 700 genes and comprises nearly 3.5% of the human genome. Chromosome 14 encodes the presinilin 1 (PSEN1) gene, which is one of the three key genes associated with the development of Alzheimer's disease (AD). The SERPINA1 gene is also located on chromosome 14 and, when defective, leads to the genetic disorder ?-antitrypsin deficiency, which is characterized by severe lung complications and liver dysfunction.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9614R-CY5.5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9614R-CY5.5
Lokale Artikelnummer::
BOSSBS-9614R-CY5.5
Beschreibung:
Chromosome 14 contains about 700 genes and 106 million base pairs and makes up about 3.5% of human cellular DNA. Chromosome 14 encodes the presinilin 1 (PSEN1) gene, which is one of the three key genes associated with the development of Alzheimer's disease. The SERPINA1 gene is located on chromosome 14 and when defective leads to the genetic disorder ?-antitrypsin deficiency. This disorder is characterized by severe lung complications and liver dysfunction. Notably, the immunoglobulin heavy chain locus is found on chromosome 14 and has been identified as a fusion with the chromosome 19 encoded protein BCL3 in the (14;19) translocations found in a variety of B cell malignancies. The C14orf140 gene product has been provisionally designated C14orf140 pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(8.21710.0100)
Lieferant:
Merck
Hersteller-Artikelnummer::
8.21710.0100
Lokale Artikelnummer::
MERC8.21710.0100
Beschreibung:
1-Bromnonan zur Synthese, Sigma-Aldrich®
VE:
1 * 100 mL
Lieferant:
GREINER BIO ONE
Beschreibung:
PS, zellkulturbehandelt, steril. In unterschiedlichen Größen und Wachstumsflächen verfügbar. Die Schalen mit 57 cm² und 143 cm² verfügen über ein besonders hohes Profil bei einer von Höhe 20 mm. Alle Schalen sind als frei von RNase, DNase und humaner DNA zertifiziert, sind nicht pyrogen und nicht zytotoxisch.
Lieferant:
GREINER BIO ONE
Beschreibung:
These sterile, PS cell culture dishes have a cell-repellent surface to effectively inhibit cell attachment. Achieved through a chemical polymer modification, the surface does not degrade or leach under common cell culture conditions, rendering an ideal substrate for native cell culture experiments.
Artikel-Nr:
(ACRO357571000)
Lieferant:
Thermo Scientific
Hersteller-Artikelnummer::
357571000
Lokale Artikelnummer::
ACRO357571000
Beschreibung:
Pelargonaldehyd 95%
VE:
1 * 100 mL
Artikel-Nr:
(BOSSBS-8226R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8226R-CY3
Lokale Artikelnummer::
BOSSBS-8226R-CY3
Beschreibung:
FAM161B is a 647 amino acid protein that belongs to the FAM161 family. The gene that encodes FAM161B consists of approximately 16,413 bases and maps to human chromosome 14q24.3. Housing over 700 genes, chromosome 14 comprises nearly 3.5% of the human genome. Chromosome 14 encodes the Presenilin 1 (PSEN1) gene, which is one of the three key genes associated with the development of Alzheimer’s disease. The SERPINA1 gene is also located on chromosome 14 and, when defective, leads to the genetic disorder α1-antitrypsin deficiency, which is characterized by severe lung complications and liver dysfunction. An inversion of the long arm of chromosome 14 is thought to be involved in T-cell chronic lymphocytic leukemia (CLL), a cancer that affects T lymphocytes.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8226R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8226R
Lokale Artikelnummer::
BOSSBS-8226R
Beschreibung:
FAM161B is a 647 amino acid protein that belongs to the FAM161 family. The gene that encodes FAM161B consists of approximately 16,413 bases and maps to human chromosome 14q24.3. Housing over 700 genes, chromosome 14 comprises nearly 3.5% of the human genome. Chromosome 14 encodes the Presenilin 1 (PSEN1) gene, which is one of the three key genes associated with the development of Alzheimer’s disease. The SERPINA1 gene is also located on chromosome 14 and, when defective, leads to the genetic disorder α1-antitrypsin deficiency, which is characterized by severe lung complications and liver dysfunction. An inversion of the long arm of chromosome 14 is thought to be involved in T-cell chronic lymphocytic leukemia (CLL), a cancer that affects T lymphocytes.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8226R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8226R-FITC
Lokale Artikelnummer::
BOSSBS-8226R-FITC
Beschreibung:
FAM161B is a 647 amino acid protein that belongs to the FAM161 family. The gene that encodes FAM161B consists of approximately 16,413 bases and maps to human chromosome 14q24.3. Housing over 700 genes, chromosome 14 comprises nearly 3.5% of the human genome. Chromosome 14 encodes the Presenilin 1 (PSEN1) gene, which is one of the three key genes associated with the development of Alzheimer’s disease. The SERPINA1 gene is also located on chromosome 14 and, when defective, leads to the genetic disorder α1-antitrypsin deficiency, which is characterized by severe lung complications and liver dysfunction. An inversion of the long arm of chromosome 14 is thought to be involved in T-cell chronic lymphocytic leukemia (CLL), a cancer that affects T lymphocytes.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8226R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8226R-HRP
Lokale Artikelnummer::
BOSSBS-8226R-HRP
Beschreibung:
FAM161B is a 647 amino acid protein that belongs to the FAM161 family. The gene that encodes FAM161B consists of approximately 16,413 bases and maps to human chromosome 14q24.3. Housing over 700 genes, chromosome 14 comprises nearly 3.5% of the human genome. Chromosome 14 encodes the Presenilin 1 (PSEN1) gene, which is one of the three key genes associated with the development of Alzheimer’s disease. The SERPINA1 gene is also located on chromosome 14 and, when defective, leads to the genetic disorder α1-antitrypsin deficiency, which is characterized by severe lung complications and liver dysfunction. An inversion of the long arm of chromosome 14 is thought to be involved in T-cell chronic lymphocytic leukemia (CLL), a cancer that affects T lymphocytes.
VE:
1 * 100 µl
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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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