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3,3\'-Iminobis(propylamin)


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Artikel-Nr: (BOSSBS-0819R-CY7)

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-0819R-CY7
Lokale Artikelnummer:: BOSSBS-0819R-CY7
Beschreibung:   Tyrosinase is the key enzyme for melanin,synthesis in mammalian melanocytes and has been considered to be a unique marker for the study of melanocyte differentiation. A cDNA library was constructed from poly(A)+ mRNA from mouse melanocytes and screened using anti- tyrosinase antiserum and oligonucleotide probes corresponding to amino acid sequence of tyrosinase. sequencing of some cDNA clones positive in these screenings gave a nucleotide sequence of 1838 nucleotides including a open reading frame of 1344 nucleotides that was found to correspond exactly to the amino acid sequence of the cyanogen bromide fragments of tyrosinase.
VE:  1 * 100 µl

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-12566R-A350
Lokale Artikelnummer:: BOSSBS-12566R-A350
Beschreibung:   ACAA1 is a 424 amino acid member of the thiolase family of enzymes and is involved in lipid metabolism. Localized to the peroxisome, ACAA1 catalyzes the conversion of acyl-CoA and acetyl-CoA to 3-oxoacyl-CoA in the fatty acid oxidation pathway. ACAA1 shows high enzymatic activity in liver, kidney, intestine and white adipose tissue in rats, where it exists as two types, namely type A and type B. Human ACAA1 shares 86% amino acid identity with its rat counterpart, suggesting a conserved function for ACAA1 among different species.
VE:  1 * 100 µl
Lieferant:  Thermo Scientific
Beschreibung:   Adenosin-5'-monophosphorsäure (AMP) 99%
Artikel-Nr: (BOSSBS-11061R-CY3)

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-11061R-CY3
Lokale Artikelnummer:: BOSSBS-11061R-CY3
Beschreibung:   OLFM3 is a 478 amino acid protein that interacts with myocilin. Myocilin is an extracellular protein that plays a key role in the actomyosin system and is responsible for controlling intraocular pressure. OLFM3 is a secreted protein that contains an olfactomedin-like (OLF) domain, an approximately 260 amino acid motif commonly found in secreted glycoproteins. OLFM3 localizes to the Golgi apparatus of the cell and is highly expressed in both eye and brain tissue. Mutations in the gene that encodes OLFM3 may cause severe glaucoma, a condition in which increased intraocular pressure within the eyeball causes loss of eye sight.
VE:  1 * 100 µl

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-6613R-A647
Lokale Artikelnummer:: BOSSBS-6613R-A647
Beschreibung:   Catalyzes the first reaction in the catabolism of the essential branched chain amino acids leucine, isoleucine, and valine.
VE:  1 * 100 µl

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-11389R-A750
Lokale Artikelnummer:: BOSSBS-11389R-A750
Beschreibung:   This protein functions in trans to edit the amino acid moiety from incorrectly charged tRNA(Ala) (by similarity). There are 2 isoforms produced by alternative splicing.
VE:  1 * 100 µl
Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-11389R-HRP
Lokale Artikelnummer:: BOSSBS-11389R-HRP
Beschreibung:   This protein functions in trans to edit the amino acid moiety from incorrectly charged tRNA(Ala) (by similariy). There are 2 isoforms produced by alternative splicing.
VE:  1 * 100 µl
Lieferant:  Alfa Aesar
Beschreibung:   N-(tert-Butoxycarbonyl)-L-tert-leucine 98%
Lieferant:  Thermo Scientific
Beschreibung:   Tetradecylamin 98%
Lieferant:  Thermo Scientific
Beschreibung:   1-Aminobenzotriazol 98%
Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-13448R-HRP
Lokale Artikelnummer:: BOSSBS-13448R-HRP
Beschreibung:   GLYCTK is a 523 amino acid protein that is expressed as seven isoforms which are present throughout the body. Localized to the cytoplasm and the mitochondrion in an isoform-specific manner, GLYCTK functions to catalyze the ATP-dependent conversion of (R)-glycerate to 3-(R)-glycerate, thereby playing an important role in neural and skeletal muscle systems. Defects in the gene encoding GLYCTK are the cause of D-glyceric acidemia, an inborn error of amino acid metabolism that is best described as nonketotic hyperglycinemia and is characterized by the excretion of D-glyceric acid in the urine.
VE:  1 * 100 µl

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-13448R-A647
Lokale Artikelnummer:: BOSSBS-13448R-A647
Beschreibung:   GLYCTK is a 523 amino acid protein that is expressed as seven isoforms which are present throughout the body. Localized to the cytoplasm and the mitochondrion in an isoform-specific manner, GLYCTK functions to catalyze the ATP-dependent conversion of (R)-glycerate to 3-(R)-glycerate, thereby playing an important role in neural and skeletal muscle systems. Defects in the gene encoding GLYCTK are the cause of D-glyceric acidemia, an inborn error of amino acid metabolism that is best described as nonketotic hyperglycinemia and is characterized by the excretion of D-glyceric acid in the urine.
VE:  1 * 100 µl
Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-6841R-FITC
Lokale Artikelnummer:: BOSSBS-6841R-FITC
Beschreibung:   This gene encodes a protein with limited similarity to L-amino acid oxidase which contains the conserved amino acids thought to be involved in catalysis and binding of flavin adenine dinucleotide (FAD) cofactor. The expression of this gene can be induced by interleukin 4 in B cells, however, expression of transcripts containing the first two exons of the upstream gene is found in other cell types. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2012].
VE:  1 * 100 µl
Lieferant:  Bioworld Technology
Hersteller-Artikelnummer:: BS2234
Lokale Artikelnummer:: BWRLBS2234
Beschreibung:   Synthetic peptide, corresponding to amino acids 600-650 of Human DNA Ligase IV.
VE:  1 * 100 µG
Lieferant:  Alfa Aesar
Beschreibung:   (R)-(-)-β-Aminophenethylalkohol ≥98%
Lieferant:  Alfa Aesar
Beschreibung:   3,4,5-Trimethoxyanthranilsäure 97%
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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