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(\\u00B1)11(12)-EET+methyl+ester
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(\\u00B1)11(12)-EET+methyl+ester
Artikel-Nr:
(BLDPBD16361-25G)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD16361-25G
Lokale Artikelnummer::
BLDPBD16361-25G
Beschreibung:
1,2-Diphenyl-1-butanon 98%
VE:
1 * 25 g
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
4-Chloro-1,2-dimethoxybenzene 95%
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
4-(Cyclohexylcarbamoyl)-3-fluorphenylboronsäure 95%
Lieferant:
Thermo Scientific
Beschreibung:
Aktivkohle, NORIT® SA 2, bleichend
Artikel-Nr:
(BOSSBS-3898R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-3898R-A680
Lokale Artikelnummer::
BOSSBS-3898R-A680
Beschreibung:
Has steroid 11-beta-hydroxylase activity. In addition to this activity, the 18 or 19-hydroxylation of steroids and the aromatization of androstendione to estrone have also been ascribed to cytochrome P45 XIB.
VE:
1 * 100 µl
Artikel-Nr:
(01419-5MG)
Lieferant:
Sigma-Aldrich
Hersteller-Artikelnummer::
01419-5MG
Lokale Artikelnummer::
SUPL01419-5MG
Beschreibung:
Organic Standard, 1,2-Propandiamin-1,2,3-¹³C₃,1-¹⁵N Hydrochlorid
VE:
1 * 5 mg
Artikel-Nr:
(BOSSBS-8087R-CY5.5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8087R-CY5.5
Lokale Artikelnummer::
BOSSBS-8087R-CY5.5
Beschreibung:
The coiled-coil domain is a structural motif found in proteins that are involved in a diverse array of biological functions such as the regulation of gene expression, cell division, membrane fusion, and drug extrusion and delivery. CCDC83 (coiled-coil domain-containing protein 83), also known as HSD9, is 413 amino acid protein that exists as three alternatively spliced isoforms. The gene encoding CCDC83 maps to human chromosome 11, which houses over 1,400 genes and comprises nearly 4% of the human genome. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are associated with defects in genes that maps to chromosome 11.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8139R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8139R-CY7
Lokale Artikelnummer::
BOSSBS-8139R-CY7
Beschreibung:
The coiled-coil domain is a structural motif found in proteins that are involved in a diverse array of biological functions such as the regulation of gene expression, cell division, membrane fusion, and drug extrusion and delivery. CCDC83 (coiled-coil domain-containing protein 83), also known as HSD9, is 413 amino acid protein that exists as three alternatively spliced isoforms. The gene encoding CCDC83 maps to human chromosome 11, which houses over 1,400 genes and comprises nearly 4% of the human genome. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are associated with defects in genes that maps to chromosome 11.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8139R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8139R-CY3
Lokale Artikelnummer::
BOSSBS-8139R-CY3
Beschreibung:
The coiled-coil domain is a structural motif found in proteins that are involved in a diverse array of biological functions such as the regulation of gene expression, cell division, membrane fusion, and drug extrusion and delivery. CCDC83 (coiled-coil domain-containing protein 83), also known as HSD9, is 413 amino acid protein that exists as three alternatively spliced isoforms. The gene encoding CCDC83 maps to human chromosome 11, which houses over 1,400 genes and comprises nearly 4% of the human genome. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are associated with defects in genes that maps to chromosome 11.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-5018R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5018R-HRP
Lokale Artikelnummer::
BOSSBS-5018R-HRP
Beschreibung:
ACADVL (acyl-Coenzyme A dehydrogenase, very long chain) catalyzes the first step of the mitochondrial fatty acid beta-oxidation pathway. It is specific to esters of long-chain and very long chain fatty acids such as palmitoyl-CoA and stearoyl-CoA. Deficiencies in ACADVL are associated with reduced myocardial fatty acid beta-oxidation and cardiomyopathy.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8141R-CY5.5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8141R-CY5.5
Lokale Artikelnummer::
BOSSBS-8141R-CY5.5
Beschreibung:
HkRP3, also known as CCDC88B (coiled-coil domain-containing protein 88B) or BRLZ (brain leucine zipper domain-containing protein), is a 1,476 amino acid protein that belongs to the CCDC88 family. Members of the hook-related protein family are characterized by the presence of a C-terminal hook-related domain and an N-terminal potential microtubule binding domain. HkRP3 may be involved in the linkage of various organelles to microtubules, and exists as six alternatively spliced isoforms. The gene encoding HkRP3 maps to human chromosome 11q13.1 and mouse chromosome 19 A. Chromosome 11 houses over 1,400 genes and comprises nearly 4% of the human genome. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are associated with defects in genes that maps to chromosome 11.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8141R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8141R-A647
Lokale Artikelnummer::
BOSSBS-8141R-A647
Beschreibung:
HkRP3, also known as CCDC88B (coiled-coil domain-containing protein 88B) or BRLZ (brain leucine zipper domain-containing protein), is a 1,476 amino acid protein that belongs to the CCDC88 family. Members of the hook-related protein family are characterized by the presence of a C-terminal hook-related domain and an N-terminal potential microtubule binding domain. HkRP3 may be involved in the linkage of various organelles to microtubules, and exists as six alternatively spliced isoforms. The gene encoding HkRP3 maps to human chromosome 11q13.1 and mouse chromosome 19 A. Chromosome 11 houses over 1,400 genes and comprises nearly 4% of the human genome. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are associated with defects in genes that maps to chromosome 11.
VE:
1 * 100 µl
Lieferant:
Alfa Aesar
Beschreibung:
1,2-Cyclohexandion ≥98%
Artikel-Nr:
(BOSSBS-6882R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-6882R-FITC
Lokale Artikelnummer::
BOSSBS-6882R-FITC
Beschreibung:
TIS11D is a member of the TIS11 family of early response genes. Family members are induced by various agonists such as the phorbol ester TPA and the polypeptide mitogen EGF. The encoded protein contains a distinguishing putative zinc finger domain with a repeating cys-his motif. This putative nuclear transcription factor most likely functions in regulating the response to growth factors.
VE:
1 * 100 µl
Artikel-Nr:
(BLDPBD01393639-5G)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD01393639-5G
Lokale Artikelnummer::
BLDPBD01393639-5G
Beschreibung:
(±)-1,2-Dodecandiol 95+%, (Chunks or flakes)
VE:
1 * 5 g
Lieferant:
Alfa Aesar
Beschreibung:
1,2-Epoxy-3-methylbutan ≥98%
Preis auf Anfrage
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.
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.
Dieses Produkt kann nur an eine Lieferadresse versandt werden die über die entsprechende Lizenzen verfügt. Für weitere Hilfe bitte kontaktieren Sie Ihr VWR Vertriebszentrum.
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