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(R)-(+)-2-Pyrrolidinon-5-carbons\\\\\\\\u00E4ure
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(R)-(+)-2-Pyrrolidinon-5-carbons\\\\\\\\u00E4ure
Artikel-Nr:
(BOSSBS-1972R-CY5.5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-1972R-CY5.5
Lokale Artikelnummer::
BOSSBS-1972R-CY5.5
Beschreibung:
Central enzyme in the extracellular metabolism of plasma lipoproteins. Synthesized mainly in the liver and secreted into plasma where it converts cholesterol and phosphatidylcholines (lecithins) to cholesteryl esters and lysophosphatidylcholines on the surface of high and low density lipoproteins (HDLs and LDLs). The cholesterol ester is then transported back to the liver. Has a preference for plasma 16:0-18:2 or 18:O-18:2 phosphatidylcholines. Also produced in the brain by primary astrocytes, and esterifies free cholesterol on nascent APOE-containing lipoproteins secreted from glia and influences cerebral spinal fluid (CSF) APOE- and APOA1 levels. Together with APOE and the cholesterol transporter ABCA1, plays a key role in the maturation of glial-derived, nascent lipoproteins. Required for remodeling high-density lipoprotein particles into their spherical forms.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-1972R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-1972R-A555
Lokale Artikelnummer::
BOSSBS-1972R-A555
Beschreibung:
Central enzyme in the extracellular metabolism of plasma lipoproteins. Synthesized mainly in the liver and secreted into plasma where it converts cholesterol and phosphatidylcholines (lecithins) to cholesteryl esters and lysophosphatidylcholines on the surface of high and low density lipoproteins (HDLs and LDLs). The cholesterol ester is then transported back to the liver. Has a preference for plasma 16:0-18:2 or 18:O-18:2 phosphatidylcholines. Also produced in the brain by primary astrocytes, and esterifies free cholesterol on nascent APOE-containing lipoproteins secreted from glia and influences cerebral spinal fluid (CSF) APOE- and APOA1 levels. Together with APOE and the cholesterol transporter ABCA1, plays a key role in the maturation of glial-derived, nascent lipoproteins. Required for remodeling high-density lipoprotein particles into their spherical forms.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-1972R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-1972R-FITC
Lokale Artikelnummer::
BOSSBS-1972R-FITC
Beschreibung:
Central enzyme in the extracellular metabolism of plasma lipoproteins. Synthesized mainly in the liver and secreted into plasma where it converts cholesterol and phosphatidylcholines (lecithins) to cholesteryl esters and lysophosphatidylcholines on the surface of high and low density lipoproteins (HDLs and LDLs). The cholesterol ester is then transported back to the liver. Has a preference for plasma 16:0-18:2 or 18:O-18:2 phosphatidylcholines. Also produced in the brain by primary astrocytes, and esterifies free cholesterol on nascent APOE-containing lipoproteins secreted from glia and influences cerebral spinal fluid (CSF) APOE- and APOA1 levels. Together with APOE and the cholesterol transporter ABCA1, plays a key role in the maturation of glial-derived, nascent lipoproteins. Required for remodeling high-density lipoprotein particles into their spherical forms.
VE:
1 * 100 µl
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
2-Brom-4-chlor-5-fluoranilin 98%
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
2-Bromo-3-(trifluoromethoxy)pyridine 95%
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
1-Chloro-3-fluoro-2-propanol 96%
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
5-Hydroxypridine-3-boronic acid 97%
Artikel-Nr:
(APOSPC510043-5G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
PC510043-5G
Lokale Artikelnummer::
APOSPC510043-5G
Beschreibung:
2-(Hydroxymethyl)-6-[4-(trifluoromethyl)phenyl]pyridine
VE:
1 * 5 g
Artikel-Nr:
(APOSOR956410-5G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR956410-5G
Lokale Artikelnummer::
APOSOR956410-5G
Beschreibung:
Ethyl 2-amino-6-chlorobenzoate 95%
VE:
1 * 5 g
Artikel-Nr:
(BSENC-1523-500)
Lieferant:
Biosensis
Hersteller-Artikelnummer::
C-1523-500
Lokale Artikelnummer::
BSENC-1523-500
Beschreibung:
Hormone Sensitive Lipase (HSL) hydrolyzes stored triglycerides to free fatty acids in adipose tissue and heart. In steroidogenic tissues, HSL principally converts cholesteryl esters to free cholesterol for steroid hormone production (ref: SWISSPROT).
VE:
1 * 500 µl
Artikel-Nr:
(BOSSBS-8199R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8199R-A750
Lokale Artikelnummer::
BOSSBS-8199R-A750
Beschreibung:
FAM168A is a 244 amino acid protein that exists as three alternatively spliced isoforms and is encoded by a gene that maps to human chromosome 11, which 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:
(APOSOR315743-5G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR315743-5G
Lokale Artikelnummer::
APOSOR315743-5G
Beschreibung:
2-(4-Chlorphenoxy)anilin 98%
VE:
1 * 5 g
Artikel-Nr:
(BOSSBS-13190R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13190R-CY5
Lokale Artikelnummer::
BOSSBS-13190R-CY5
Beschreibung:
Fas ligand associated factor 1; Fas ligand-associated factor 1; FBP 11; FBP11; FLAF 1; FLAF1; FNBP 3; Formin binding protein 11; Formin binding protein 3; Formin-binding protein 11; Formin-binding protein 3; HIP-10; HIP10; Huntingtin interacting protein A; Huntingtin interacting protein HYPA; Huntingtin yeast partner A; Huntingtin-interacting protein 10; Huntingtin-interacting protein A; HYPA; NY REN 6; NY REN 6 antigen; PR40A_HUMAN; Pre mRNA processing factor 40 homolog A; Pre-mRNA-processing factor 40 homolog A; PRP40 pre mRNA processing factor 40 homolog A (S cerevisiae); PRP40 pre mRNA processing factor 40 homolog A (yeast); PRP40 pre mRNA processing factor 40 homolog A; PRPF 40A; PRPF40A; Renal carcinoma antigen NY-REN-6.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-6758R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-6758R-CY3
Lokale Artikelnummer::
BOSSBS-6758R-CY3
Beschreibung:
Mtvr1 is a 176 amino acid protein that exists as two alternatively spliced isoforms. Belonging to the FAM89 family, Mtvr1 is encoded by a gene that maps to human chromosome 11, which comprises approximately 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-encoded genes.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-6758R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-6758R-A350
Lokale Artikelnummer::
BOSSBS-6758R-A350
Beschreibung:
Mtvr1 is a 176 amino acid protein that exists as two alternatively spliced isoforms. Belonging to the FAM89 family, Mtvr1 is encoded by a gene that maps to human chromosome 11, which comprises approximately 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-encoded genes.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9659R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9659R-A647
Lokale Artikelnummer::
BOSSBS-9659R-A647
Beschreibung:
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 β 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. The FAM76B gene product has been provisionally designated FAM76B pending further characterization.
VE:
1 * 100 µl
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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
noch angezeigt wird und Sie Hilfe benötigen, rufen Sie uns an 1-800-932 - 5000.
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