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5-Chlorobenzo[b]thiophene-3-acetic+acid


39 372  results were found

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Lieferant:  Sigma-Aldrich
Hersteller-Artikelnummer:: 104426-5G
Lokale Artikelnummer:: SIAL104426-5G
Beschreibung:   Tetrafluorterephthalonitril, Sigma-Aldrich®
VE:  1 * 5 g
Lieferant:  BIOLEGEND INC
Beschreibung:   Anti-CD279 (PD-1) Rat Monoclonal Antibody [clone: RMP1-14]
Lieferant:  Sigma-Aldrich
Beschreibung:   L(+)-Asparagin Monohydrat, Sigma-Aldrich®

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-9258R-A680
Lokale Artikelnummer:: BOSSBS-9258R-A680
Beschreibung:   The RING-type zinc finger motif is present in a number of viral and eukaryotic proteins and is made of a conserved cysteine-rich domain that is able to bind two zinc atoms. Proteins that contain this conserved domain are generally involved in protein-protein interactions and protein-DNA interactions. Specifically, they are thought to be involved in the ubiquitination pathway of protein degradation. RNF165 (RING finger protein 165) is a 346 amino acid protein that contains one RING-type zinc finger. Via its RING-type zinc finger, RNF165 may play a role in transcriptional regulation and protein degradation events. The gene encoding RNF165 maps to human chromosome 18, which houses over 300 genes, including Trisomy 18, or Edwards syndrome, the second most common trisomy after Downs syndrome. Translocation between chromosome 18 and 14 is the most common translocation in cancers, and occurs in follicular lymphomas. Niemann-Pick disease, hereditary hemorrhagic telangiectasia and erythropoietic protoporphyria are also associated with chromosome 18.
VE:  1 * 100 µl

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-11073R-A750
Lokale Artikelnummer:: BOSSBS-11073R-A750
Beschreibung:   The cadherins are a family of Ca2+-dependent adhesion molecules that function to mediate cell-cell binding events that are critical to the maintenance of cell structure and morphogenesis. EY-cadherin, also known as CDH18 (cadherin 18), CDH14 (cadherin 14), CDH24 or CDH14L, is a 790 amino acid single-pass type I membrane protein that contains five cadherin domains. One of several members of the cadherin superfamily, EY-cadherin functions as a type II classical cadherin that is expressed specifically in the central nervous system (CNS), where it plays a role in cell-cell binding events. Specifically, EY-cadherin is thought to be involved in axon guidance and outgrowth, as well as synaptic adhesion within the CNS. EY-cadherin contains a highly conserved C-terminal domain characteristic of all cadherins, but lacks the HAV cell adhesion sequence that is specific to type I cadherins. The gene encoding EY-cadherin is located within a region on chromosome five that is commonly deleted in carcinomas, implicating EY-cadherin as a potential tumour suppressor.
VE:  1 * 100 µl

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-9258R-A750
Lokale Artikelnummer:: BOSSBS-9258R-A750
Beschreibung:   The RING-type zinc finger motif is present in a number of viral and eukaryotic proteins and is made of a conserved cysteine-rich domain that is able to bind two zinc atoms. Proteins that contain this conserved domain are generally involved in protein-protein interactions and protein-DNA interactions. Specifically, they are thought to be involved in the ubiquitination pathway of protein degradation. RNF165 (RING finger protein 165) is a 346 amino acid protein that contains one RING-type zinc finger. Via its RING-type zinc finger, RNF165 may play a role in transcriptional regulation and protein degradation events. The gene encoding RNF165 maps to human chromosome 18, which houses over 300 genes, including Trisomy 18, or Edwards syndrome, the second most common trisomy after Downs syndrome. Translocation between chromosome 18 and 14 is the most common translocation in cancers, and occurs in follicular lymphomas. Niemann-Pick disease, hereditary hemorrhagic telangiectasia and erythropoietic protoporphyria are also associated with chromosome 18.
VE:  1 * 100 µl

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-4032R-A555
Lokale Artikelnummer:: BOSSBS-4032R-A555
Beschreibung:   Phosphorylase kinase is a polymer of 16 subunits, four each of alpha, beta, gamma and delta. The alpha subunit includes the skeletal muscle and hepatic isoforms, encoded by two different genes. The beta subunit is the same in both the muscle and hepatic isoforms, encoded by this gene, which is a member of the phosphorylase b kinase regulatory subunit family. The gamma subunit also includes the skeletal muscle and hepatic isoforms, encoded by two different genes. The delta subunit is a calmodulin and can be encoded by three different genes. The gamma subunits contain the active site of the enzyme, whereas the alpha and beta subunits have regulatory functions controlled by phosphorylation. The delta subunit mediates the dependence of the enzyme on calcium concentration. Mutations in this gene cause glycogen storage disease type 9B, also known as phosphorylase kinase deficiency of liver and muscle. Alternatively spliced transcript variants encoding different isoforms have been identified in this gene. Two pseudogenes have been found on chromosomes 14 and 20, respectively.[provided by RefSeq, Feb 2010].
VE:  1 * 100 µl
Artikel-Nr: (BOSSBS-4032R-CY3)

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-4032R-CY3
Lokale Artikelnummer:: BOSSBS-4032R-CY3
Beschreibung:   Phosphorylase kinase is a polymer of 16 subunits, four each of alpha, beta, gamma and delta. The alpha subunit includes the skeletal muscle and hepatic isoforms, encoded by two different genes. The beta subunit is the same in both the muscle and hepatic isoforms, encoded by this gene, which is a member of the phosphorylase b kinase regulatory subunit family. The gamma subunit also includes the skeletal muscle and hepatic isoforms, encoded by two different genes. The delta subunit is a calmodulin and can be encoded by three different genes. The gamma subunits contain the active site of the enzyme, whereas the alpha and beta subunits have regulatory functions controlled by phosphorylation. The delta subunit mediates the dependence of the enzyme on calcium concentration. Mutations in this gene cause glycogen storage disease type 9B, also known as phosphorylase kinase deficiency of liver and muscle. Alternatively spliced transcript variants encoding different isoforms have been identified in this gene. Two pseudogenes have been found on chromosomes 14 and 20, respectively.[provided by RefSeq, Feb 2010].
VE:  1 * 100 µl

Lieferant:  US Biological
Hersteller-Artikelnummer:: 135545
Lokale Artikelnummer:: USBI135545
Beschreibung:   Anti-ZBTB14 Mouse Polyclonal Antibody
VE:  1 * 50 µG
Artikel-Nr: (EHERC12370100)

Lieferant:  EHRENSTORFER
Hersteller-Artikelnummer:: C12370100
Lokale Artikelnummer:: EHERC12370100
Beschreibung:   p-Xylol-[D10]
VE:  1 * 100 mg
Artikel-Nr: (EHERC12170400)

Lieferant:  EHRENSTORFER
Hersteller-Artikelnummer:: C12170400
Lokale Artikelnummer:: EHERC12170400
Beschreibung:   Dexamethason
VE:  1 * 0,1 g
Artikel-Nr: (233-5615)

Lieferant:  MARTOR ARGENTAX
Hersteller-Artikelnummer:: 14.50
Lokale Artikelnummer:: MARO14.50
Beschreibung:   Blades for use in scalpels.
VE:  1 * 10 ST
Lieferant:  IMMUNOLOGIC
Beschreibung:   Anti-CTNNB1 Mouse Monoclonal Antibody [clone: 14]
Lieferant:  Serva
Beschreibung:   Dithiothreitol (DTT, Cleland's Reagenz)
Lieferant:  Serva
Beschreibung:   Dithiothreitol (DTT, Cleland's Reagenz)

Lieferant:  ProSci Inc.
Hersteller-Artikelnummer:: 92-153
Lokale Artikelnummer:: PRSI92-153
Beschreibung:   Caspase 14 (CASP14) is an enzyme that belongs to the peptidase C14A family. The Caspase 14 protein is complexed of unprocessed caspase-14 and processed 19 kDa (p19) and 10 kDa (p10) subunits. Sequential activation of caspases plays a central role in the execution-phase of cell apoptosis. Caspases exist as inactive proenzymes, which undergo proteolytic processing at conserved aspartic residues to produce two subunits, large and small, that dimerise to form the active enzyme. CASP14 has been shown to be processed and activated by Caspase 8 and Caspase 10 in vitro, and by anti-Fas agonist antibody or TNF-related apoptosis inducing ligand in vivo. The expression and processing of this caspase may be involved in keratinocyte terminal differentiation, which is important for the formation of the skin barrier. It is believed to be a non-apoptotic caspase which is involved in epidermal differentiation, keratinocyte differentiation and cornification. CASP14 probably regulates maturation of the epidermis by proteolytically processing filaggrin.
VE:  1 * 50 µG
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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