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(\\u00B1)11(12)-EET+methyl+ester


130 189  results were found

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Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-3145R-A555
Lokale Artikelnummer:: BOSSBS-3145R-A555
Beschreibung:   This gene encodes a member of the O class of winged helix/forkhead transcription factor family. Proteins encoded by this class are regulated by factors involved in growth and differentiation indicating they play a role in these processes. A translocation involving this gene on chromosome X and the homolog of the Drosophila trithorax gene, encoding a DNA binding protein, located on chromosome 11 is associated with leukemia. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2010]
VE:  1 * 100 µl
Artikel-Nr: (EHERC20001100)

Lieferant:  EHRENSTORFER
Hersteller-Artikelnummer:: C20001100
Lokale Artikelnummer:: EHERC20001100
Beschreibung:   3,3'-Dichlorbiphenyl (PCB Nr. 11)
VE:  1 * 25 mg
Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-2311R-A555
Lokale Artikelnummer:: BOSSBS-2311R-A555
Beschreibung:   Classical swine fever(CSF) is a kind of acute and intense contagious disease in swine, it material damages swine industry. CSF could cause swine appearing disseminated hemorrhage in systemic organ and tissue, degeneration and necrosis in small vascular and capillary endothelial cells. Classical swine fever virus (CSFV) belongs to genera Pestivirus, family Flaviviridae, it’s genome total length is 12.3Kb,including a big ORF, encoding 11 structural and nonstructural proteins.
VE:  1 * 100 µl
Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-4041R-A750
Lokale Artikelnummer:: BOSSBS-4041R-A750
Beschreibung:   Transaldolase 1 is a key enzyme of the nonoxidative pentose phosphate pathway providing ribose-5-phosphate for nucleic acid synthesis and NADPH for lipid biosynthesis. This pathway can also maintain glutathione at a reduced state and thus protect sulfhydryl groups and cellular integrity from oxygen radicals. The functional gene of transaldolase 1 is located on chromosome 11 and a pseudogene is identified on chromosome 1 but there are conflicting map locations. The second and third exon of this gene were developed by insertion of a retrotransposable element. This gene is thought to be involved in multiple sclerosis.
VE:  1 * 100 µl

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-4041R-CY5.5
Lokale Artikelnummer:: BOSSBS-4041R-CY5.5
Beschreibung:   Transaldolase 1 is a key enzyme of the nonoxidative pentose phosphate pathway providing ribose-5-phosphate for nucleic acid synthesis and NADPH for lipid biosynthesis. This pathway can also maintain glutathione at a reduced state and thus protect sulfhydryl groups and cellular integrity from oxygen radicals. The functional gene of transaldolase 1 is located on chromosome 11 and a pseudogene is identified on chromosome 1 but there are conflicting map locations. The second and third exon of this gene were developed by insertion of a retrotransposable element. This gene is thought to be involved in multiple sclerosis.
VE:  1 * 100 µl
Lieferant:  BLD PHARMATECH GMBH
Hersteller-Artikelnummer:: BD159603-1G
Lokale Artikelnummer:: BLDPBD159603-1G
Beschreibung:   tert-Butyl 6-chloro-2-oxo-1,2-dihydrospiro[benzo[d][1,3]oxazine-4,4'-piperidine]-1'-carboxylate 98%
VE:  1 * 1 g
Artikel-Nr: (8.41595.0025)

Lieferant:  Merck
Hersteller-Artikelnummer:: 8.41595.0025
Lokale Artikelnummer:: MERC8.41595.0025
Beschreibung:   4,4'-Anisoin zur Synthese
VE:  1 * 25 g

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-15518R-A750
Lokale Artikelnummer:: BOSSBS-15518R-A750
Beschreibung:   IFITM5 is a membrane protein thought to play a role in bone mineralisation. This gene is located on chromosome 11 in a cluster of related genes which are induced by interferon, however, this gene has not been shown to be interferon inducible. A similar gene, located in a gene cluster on mouse chromosome 7, is a member of the interferon-inducible fragilis gene family. The mouse gene encodes a transmembrane protein described as participating in germ cell competence. A mutation in the 5' UTR of this gene has been associated with osteogenesis imperfecta type V (PMID: 22863190, 22863195).
VE:  1 * 100 µl

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-15518R-A488
Lokale Artikelnummer:: BOSSBS-15518R-A488
Beschreibung:   IFITM5 is a membrane protein thought to play a role in bone mineralisation. This gene is located on chromosome 11 in a cluster of related genes which are induced by interferon, however, this gene has not been shown to be interferon inducible. A similar gene, located in a gene cluster on mouse chromosome 7, is a member of the interferon-inducible fragilis gene family. The mouse gene encodes a transmembrane protein described as participating in germ cell competence. A mutation in the 5' UTR of this gene has been associated with osteogenesis imperfecta type V (PMID: 22863190, 22863195).
VE:  1 * 100 µl
Artikel-Nr: (BOSSBS-15518R-HRP)

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-15518R-HRP
Lokale Artikelnummer:: BOSSBS-15518R-HRP
Beschreibung:   IFITM5 is a membrane protein thought to play a role in bone mineralisation. This gene is located on chromosome 11 in a cluster of related genes which are induced by interferon, however, this gene has not been shown to be interferon inducible. A similar gene, located in a gene cluster on mouse chromosome 7, is a member of the interferon-inducible fragilis gene family. The mouse gene encodes a transmembrane protein described as participating in germ cell competence. A mutation in the 5' UTR of this gene has been associated with osteogenesis imperfecta type V (PMID: 22863190, 22863195).
VE:  1 * 100 µl
Artikel-Nr: (BOSSBS-13055R-CY3)

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-13055R-CY3
Lokale Artikelnummer:: BOSSBS-13055R-CY3
Beschreibung:   This gene encodes a subunit of the elongation factor-1complex, which is responsible for the enzymatic delivery ofaminoacyl tRNAs to the ribosome. This subunit, delta, functions asguanine nucleotide exchange factor. It is reported that followingHIV-1 infection, this subunit interacts with HIV-1 Tat. Thisinteraction results in repression of translation of host cellproteins and enhanced translation of viral proteins. Severalalternatively spliced transcript variants encoding multipleisoforms have been found for this gene. Related pseudogenes havebeen defined on chromosomes 1, 6, 7, 9, 11, 13, 17, 19.[provided byRefSeq, Aug 2010].
VE:  1 * 100 µl
Artikel-Nr: (BOSSBS-15518R-FITC)

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-15518R-FITC
Lokale Artikelnummer:: BOSSBS-15518R-FITC
Beschreibung:   IFITM5 is a membrane protein thought to play a role in bone mineralisation. This gene is located on chromosome 11 in a cluster of related genes which are induced by interferon, however, this gene has not been shown to be interferon inducible. A similar gene, located in a gene cluster on mouse chromosome 7, is a member of the interferon-inducible fragilis gene family. The mouse gene encodes a transmembrane protein described as participating in germ cell competence. A mutation in the 5' UTR of this gene has been associated with osteogenesis imperfecta type V (PMID: 22863190, 22863195).
VE:  1 * 100 µl
Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-11756R-A750
Lokale Artikelnummer:: BOSSBS-11756R-A750
Beschreibung:   Sulfatases are enzymes that hydrolyse a diverse range of sulfate esters. Deficiency of lysosomal sulfatases leads to human diseases characterised by the accumulation of either GAGs (glycosaminoglycans) or sulfolipids. Sulfamidase, also known as HSS, SFMD, MPS3A or SGSH, is a 502 amino acid lysosome that belongs to the sulfatase family. It has been suggested that sulfamidase may be involved in the lysosomal degradation of heparan sulfate. Defects in the gene encoding sulfamidase are the cause of Sanfilippo syndrome A, an autosomal recessive lysosomal storage disease caused by impaired degradation of heparan sulfate. Sanfilippo syndrome A is characterised by severe central nervous system degeneration but relatively mild somatic manifestations.
VE:  1 * 100 µl
Lieferant:  Sigma-Aldrich
Beschreibung:   11-Brom-1-undecen, Sigma-Aldrich®
Lieferant:  Bioss
Hersteller-Artikelnummer:: BSM-0861M-A680
Lokale Artikelnummer:: BOSSBSM-0861M-A680
Beschreibung:   2,4-Dichlorophenoxyacetic acid (2,4-D) is a common systemic herbicide used in the control of broadleaf weeds. It is the most widely used herbicide in the world, and the third most commonly used in North America. 2,4-D is also an important synthetic auxin, often used in laboratories for plant research and as a supplement in plant cell culture media such as MS medium. 2,4-D is a synthetic auxin, which is a class of plant growth regulators. It is absorbed through the leaves and is translocated to the meristems of the plant. Uncontrolled, unsustainable growth ensues causing stem curl-over, leaf withering, and eventual plant death. 2,4-D is typically applied as an amine salt, but more potent ester versions exist as well.
VE:  1 * 100 µl

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-0861R-CY7
Lokale Artikelnummer:: BOSSBS-0861R-CY7
Beschreibung:   2,4-Dichlorophenoxyacetic acid (2,4-D) is a common systemic herbicide used in the control of broadleaf weeds. It is the most widely used herbicide in the world, and the third most commonly used in North America. [1] 2,4-D is also an important synthetic auxin, often used in laboratories for plant research and as a supplement in plant cell culture media such as MS medium. 2,4-D is a synthetic auxin, which is a class of plant growth regulators. It is absorbed through the leaves and is translocated to the meristems of the plant. Uncontrolled, unsustainable growth ensues causing stem curl-over, leaf withering, and eventual plant death. 2,4-D is typically applied as an amine salt, but more potent ester versions exist as well.
VE:  1 * 100 µl
Preis auf Anfrage
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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 call noch angezeigt wird und Sie Hilfe benötigen, rufen Sie uns an 1-800-932 - 5000.
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