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2'-Deoxyuridine-5'-triphosphate+trisodium+salt


14 495  results were found

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Lieferant:  Strem Chemicals, Inc.
Hersteller-Artikelnummer:: 45-0380-5G
Lokale Artikelnummer:: STRE45-0380-5G
Beschreibung:   Chlor(1,5-cyclooctadien)rhodium(I) dimer ≥98%
VE:  1 * 5 g
Market Source Item This is a MarketSource item. Additional charges may apply
Lieferant:  Sartorius
Beschreibung:   The dispenser fully automatically releases membrane filters from their sterile packaging. You can choose one of the following modes: Push button, foot switch or sensor mode.
Artikel-Nr: (BOSSBS-9161R-CY5.5)

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-9161R-CY5.5
Lokale Artikelnummer:: BOSSBS-9161R-CY5.5
Beschreibung:   The tripartite motif (TRIM) family of proteins are characterized by a conserved TRIM domain that includes a coiled-coil region, a B-box type zinc finger, one RING finger and three zinc-binding domains. TRIM17 (tripartite motif-containing 17), also known as RBCC, terf or RNF16, is a 477 amino acid protein that contains one RING-type zinc finger, one SPRY domain and one B box-type zinc finger. Expressed nearly exclusively in testis, TRIM17 belongs to the TRIM family and, based on its functional domains, may play a role in transcriptional regulation events. The gene encoding TRIM17 maps to human chromosome 1, which spans 260 million base pairs, contains over 3,000 genes and comprises nearly 8% of the human genome. Chromosome 1 houses a large number of disease-associated genes, including those that are involved in familial adenomatous polyposis, Stickler syndrome, Parkinson’s disease, Gaucher disease, schizophrenia and Usher syndrome. Aberrations in chromosome 1 are found in a variety of cancers, including head and neck cancer, malignant melanoma and multiple myeloma.
VE:  1 * 100 µl
Artikel-Nr: (L15819.06)

Lieferant:  Alfa Aesar
Hersteller-Artikelnummer:: L15819.06
Lokale Artikelnummer:: ALFAL15819.06
Beschreibung:   6-Methoxy-1-indanon ≥99%
VE:  1 * 5 g
Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-13387R-HRP
Lokale Artikelnummer:: BOSSBS-13387R-HRP
Beschreibung:   Glucose Oxidase is a dimeric enzyme that binds to β-D-glucose and aids in its oxidation into D-glucono-1,5-lactone which then hydrolyzes to gluconic acid. Flavin adenine dinucleotide (FAD) is a cofactor to Glucose Oxidase that acts as the initial electron acceptor and is required for this oxidation to occur. Glucose Oxidase is a natural preservative found in honey, where it reduces atmospheric oxygen into hydrogen peroxide which acts as an antibacterial barrier. Glucose Oxidase is also commonly used in biosensors in which it conveys levels of glucose by keeping track of the number of electrons passed through the enzyme. In this application, Glucose Oxidase is connected to an electrode and the resulting charge is measured.
VE:  1 * 100 µl
Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-13387R-FITC
Lokale Artikelnummer:: BOSSBS-13387R-FITC
Beschreibung:   Glucose Oxidase is a dimeric enzyme that binds to β-D-glucose and aids in its oxidation into D-glucono-1,5-lactone which then hydrolyzes to gluconic acid. Flavin adenine dinucleotide (FAD) is a cofactor to Glucose Oxidase that acts as the initial electron acceptor and is required for this oxidation to occur. Glucose Oxidase is a natural preservative found in honey, where it reduces atmospheric oxygen into hydrogen peroxide which acts as an antibacterial barrier. Glucose Oxidase is also commonly used in biosensors in which it conveys levels of glucose by keeping track of the number of electrons passed through the enzyme. In this application, Glucose Oxidase is connected to an electrode and the resulting charge is measured.
VE:  1 * 100 µl
Lieferant:  Thermo Scientific
Beschreibung:   CAS No.: 6160-78-7
Artikel-Nr: (BLDPBD77005-5G)

Lieferant:  BLD PHARMATECH GMBH
Hersteller-Artikelnummer:: BD77005-5G
Lokale Artikelnummer:: BLDPBD77005-5G
Beschreibung:   2-Methyl-4-undecanon 98%
VE:  1 * 5 g

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-11825R-A680
Lokale Artikelnummer:: BOSSBS-11825R-A680
Beschreibung:   DOCK 7 is a 2140 amino acid protein that localizes to developing axons and contains one DHR-1 domain and one DHR-2 domain. Expressed in a variety of tissues, DOCK 7 functions as a guanine nucleotide exchange factor (GEF) that specifically activates Rac 1 and Rac 3 by catalyzing the exchange of bound GDP for free GTP. Multiple isoforms of DOCK 7 exist due to alternative splicing events.
VE:  1 * 100 µl

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-11825R-A750
Lokale Artikelnummer:: BOSSBS-11825R-A750
Beschreibung:   DOCK 7 is a 2140 amino acid protein that localizes to developing axons and contains one DHR-1 domain and one DHR-2 domain. Expressed in a variety of tissues, DOCK 7 functions as a guanine nucleotide exchange factor (GEF) that specifically activates Rac 1 and Rac 3 by catalyzing the exchange of bound GDP for free GTP. Multiple isoforms of DOCK 7 exist due to alternative splicing events.
VE:  1 * 100 µl
Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-11825R-HRP
Lokale Artikelnummer:: BOSSBS-11825R-HRP
Beschreibung:   DOCK 7 is a 2,140 amino acid protein that localizes to developing axons and contains one DHR-1 domain and one DHR-2 domain. Expressed in a variety of tissues, DOCK 7 functions as a guanine nucleotide exchange factor (GEF) that specifically activates Rac 1 and Rac 3 by catalyzing the exchange of bound GDP for free GTP. Multiple isoforms of DOCK 7 exist due to alternative splicing events.
VE:  1 * 100 µl
Lieferant:  Thermo Scientific
Beschreibung:   Appearance: Beige Powder
Artikel-Nr: (BOSSBS-9162R)

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-9162R
Lokale Artikelnummer:: BOSSBS-9162R
Beschreibung:   The tripartite motif (TRIM) family of proteins are characterized by a conserved TRIM domain that includes a coiled-coil region, a B-box type zinc finger, one RING finger and three zinc-binding domains. TRIM17 (tripartite motif-containing 17), also known as RBCC, terf or RNF16, is a 477 amino acid protein that contains one RING-type zinc finger, one SPRY domain and one B box-type zinc finger. Expressed nearly exclusively in testis, TRIM17 belongs to the TRIM family and, based on its functional domains, may play a role in transcriptional regulation events. The gene encoding TRIM17 maps to human chromosome 1, which spans 260 million base pairs, contains over 3,000 genes and comprises nearly 8% of the human genome. Chromosome 1 houses a large number of disease-associated genes, including those that are involved in familial adenomatous polyposis, Stickler syndrome, Parkinson’s disease, Gaucher disease, schizophrenia and Usher syndrome. Aberrations in chromosome 1 are found in a variety of cancers, including head and neck cancer, malignant melanoma and multiple myeloma
VE:  1 * 100 µl
Lieferant:  Alfa Aesar
Beschreibung:   2',4'-Dihydroxy-3'-methylacetophenon ≥98%
Artikel-Nr: (BOSSBS-9350R)

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-9350R
Lokale Artikelnummer:: BOSSBS-9350R
Beschreibung:   Ubiquitin-dependent proteolysis mediates selective destruction of various cell cycle regulators, transcription factors and tumor suppressors. In eukaryotic cells, selective breakdown of cellular proteins is ensured by their ubiquitination and subsequent degradation by the 26S proteasome. At specific stages of development, embryo- and tissue-specific components of the 26S proteasome form, facilitating proteolysis. 20S Proteasome ?, also designated macropain subunit C2 or PROS-30, is a prosomal protein involved in a non-lysosomal ATP/ubiquitin-dependent proteolytic pathway. The entire proteasome is composed of at least 15 non-identical subunits which form a highly-ordered ring-shaped structure.
VE:  1 * 100 µl
Artikel-Nr: (BOSSBS-11785R)

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-11785R
Lokale Artikelnummer:: BOSSBS-11785R
Beschreibung:   Maspardin is a 308 amino acid cytoplasmic protein that is widely expressed. Belonging to the AB hydrolase superfamily, Maspardin colocalizes with CD4 on endosomal/trans-Golgi network. It is thought that Maspardin may act as a negative regulatory factor in CD4-dependent T-cell activation. Defects in the gene encoding Maspardin are the result of hereditary spastic paraplegia autosomal recessive type 21 (also designated Mast syndrome), an autosomal recessive neurodegenerative disorder characterized by a slow, gradual, progressive weakness and spasticity of the lower limbs. The gene encoding Maspardin is encoded by human chromosome 15, which houses over 700 genes and comprises nearly 3% of the human genome.
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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