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3-Methyl-5-(trifluoromethyl)cinnamic+acid


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Lieferant:  Alfa Aesar
Beschreibung:   4-Biphenylmethanol ≥98%
Lieferant:  SIGMA ALDRICH MICROSCOPY
Hersteller-Artikelnummer:: 442828-1G
Lokale Artikelnummer:: SIAM442828-1G
Beschreibung:   3,6-Dichloro-1,2-benzenedithiol has been used as a ligand in thiolate complexes, and a series of homochalcogenide and mixed-chalcogenide ligand complexes.
VE:  1 * 1 g
Lieferant:  Alfa Aesar
Beschreibung:   4,4'-Biphenol ≥99%

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-12068R-A750
Lokale Artikelnummer:: BOSSBS-12068R-A750
Beschreibung:   TMEM132A is a 560 amino acid protein encoded by a gene mapping to human chromosome 11. With approximately 135 million base pairs and 1400 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 thalassemia are caused by HBB gene mutations. Wilms' tumours, 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
Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-12068R-HRP
Lokale Artikelnummer:: BOSSBS-12068R-HRP
Beschreibung:   TMEM132A is a 560 amino acid protein encoded by a gene mapping to human chromosome 11. 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 ∫ 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

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-9932R-A750
Lokale Artikelnummer:: BOSSBS-9932R-A750
Beschreibung:   C11orf46, also known as FLJ38968 or dJ299F11.1, is a 260 amino acid protein that is encoded by a gene located on human chromosome 11. With approximately 135 million base pairs and 1400 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 _ thalassemia are caused by HBB gene mutations. Wilms' tumours, 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
Lieferant:  APOLLO SCIENTIFIC
Beschreibung:   4-Acetamido-3-fluorobenzoic acid 97%
Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-2305R-HRP
Lokale Artikelnummer:: BOSSBS-2305R-HRP
Beschreibung:   E2 EPF is a member of the ubiquitin conjugating enzyme family. It is able to form a thiol ester linkage with ubiquitin in a ubiquitin activating enzyme dependent manner, a characteristic property of ubiquitin carrier proteins.
VE:  1 * 100 µl
Lieferant:  SGE Analytical Science
Beschreibung:   Electronic battery crimping tools effortlessly crimp/decap aluminum and 2-part aluminum/steel caps with just the push of a button.
Artikel-Nr: (BLDPBD33926-1G)

Lieferant:  BLD PHARMATECH GMBH
Hersteller-Artikelnummer:: BD33926-1G
Lokale Artikelnummer:: BLDPBD33926-1G
Beschreibung:   Pyridine-2,3,4-triamine 98%
VE:  1 * 1 g

Lieferant:  BLD PHARMATECH GMBH
Hersteller-Artikelnummer:: BD295057-1G
Lokale Artikelnummer:: BLDPBD295057-1G
Beschreibung:   (S)-Hexahydropyridazine-3-carboxylic acid 95%
VE:  1 * 1 g

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-5020R-A647
Lokale Artikelnummer:: BOSSBS-5020R-A647
Beschreibung:   Plays a role in lipoprotein assembly and dietary cholesterol absorption. In addition to its acyltransferase activity, it may act as a ligase. May provide cholesteryl esters for lipoprotein secretion from hepatocytes and intestinal mucosa.
VE:  1 * 100 µl
Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-5020R-FITC
Lokale Artikelnummer:: BOSSBS-5020R-FITC
Beschreibung:   Plays a role in lipoprotein assembly and dietary cholesterol absorption. In addition to its acyltransferase activity, it may act as a ligase. May provide cholesteryl esters for lipoprotein secretion from hepatocytes and intestinal mucosa.
VE:  1 * 100 µl

Lieferant:  ANSELL HEALTH CARE
Hersteller-Artikelnummer:: 37-300/11
Lokale Artikelnummer:: ANSE37-300/11
Beschreibung:   Improved grip, dexterity, and flexibility.
VE:  1 * 12 PAAR
Lieferant:  APOLLO SCIENTIFIC
Beschreibung:   2,3'-Difluorbenzophenon 97%
Artikel-Nr: (BLDPBD232701-250MG)

Lieferant:  BLD PHARMATECH GMBH
Hersteller-Artikelnummer:: BD232701-250MG
Lokale Artikelnummer:: BLDPBD232701-250MG
Beschreibung:   5-(Methylthio)thiazol-2-amine 95%
VE:  1 * 250 mg
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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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