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4-Bromo-2-chlorobenzo[d]thiazole


153 452  results were found

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Artikel-Nr: (BOSSBS-13202R)

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-13202R
Lokale Artikelnummer:: BOSSBS-13202R
Beschreibung:   Xenopus winged-helix factor, xFAST-1 (forkhead activin signal transducer-1) is a transcription factor that forms a complex with the receptor-regulated Smad protein, Smad2, and directly binds to activin response elements on DNA (1,2). The human homolog FAST-1 and the corresponding mouse homolog, designated FAST-2, share significant sequence homology with xFAST-1, including a conserved N-terminal forkhead domain that consists of 110 amino acid residues and is essential for binding DNA and regulating transcription in embryogenesis, in tumorigenesis and in the maintenance of differentiated cell states (3,4). FAST-1 and FAST-2 also contain a distinct C-terminal Smad interaction domain that is required for the association with various Smad proteins, including Smad2, Smad3 and Smad4 (3,5). Expression of FAST-1 and FAST-2 is predominantly observed during early development, with lower levels detected in adult tissues (6,7). FAST-1 and FAST-2 mediated DNA binding is attenuated by both TFGß and activin, indicating that these FAST proteins mediate TFGß induced signal transduction (3).
VE:  1 * 100 µl
Artikel-Nr: (BOSSBS-11604R-CY7)

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-11604R-CY7
Lokale Artikelnummer:: BOSSBS-11604R-CY7
Beschreibung:   Na+/Cl- dependent neurotransmitter transporters are a superfamily of transmembrane proteins that contain 12 membrane spanning regions (1). Specifically, the highly hydrophobic Na+/Cl- dependent glycine transporters (GlyT) are crucial for the termination of neurotransmission at glycinergic synapses (2,3). Two different GlyT genes encode GlyT2 and GlyT1, which exists as two isoforms produced by alternative splicing of the same gene located on human chromosome 1p31.3 (3,4). The GlyT1 gene may be an early marker of neural development and encodes glia-specific transporter proteins (3). Although GlyT1 and GlyT2 are both expressed in the brain and spinal cord, each shows a unique pattern of expression (3,5,6). GlyT1 is found only in the white matter of the CNS, whereas GlyT2 is found in the gray matter of the CNS as well as in macrophages and mast cells in peripheral tissues (3,5). The anatomic distribution of GlyT2 mRNA suggests that glycine may act as a supraspinal neurotransmitter and may function as a chemical messenger outside the CNS (5).
VE:  1 * 100 µl
Lieferant:  Thermo Scientific
Beschreibung:   N,N,N',N'-Tetramethylethylendiamin (TEMED) 99%, reinst
Artikel-Nr: (MOLEM61936762)

Lieferant:  Molekula
Hersteller-Artikelnummer:: M61936762
Lokale Artikelnummer:: MOLEM61936762
Beschreibung:   2-Hydroxynicotinsäure
VE:  1 * 25 g
Market Source Item This is a MarketSource item. Additional charges may apply

Lieferant:  Sigma-Aldrich
Hersteller-Artikelnummer:: A6435-100G
Lokale Artikelnummer:: SIALA6435-100G
Beschreibung:   Aluminiumkaliumsulfat Dodecahydrat, Sigma-Aldrich®
VE:  1 * 100 g
Lieferant:  Alfa Aesar
Beschreibung:   Aluminiumammoniumsulfat Dodecahydrat, Reagenzqualität

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-15154R-CY7
Lokale Artikelnummer:: BOSSBS-15154R-CY7
Beschreibung:   C12orf56 (chromosome 12 open reading frame 56), also known as PRO1853 or protein midA homolog, is a 441 amino acid mitochondrial protein that belongs to the midA family. Existing as two alternatively spliced isoforms, C12orf56 is encoded by a gene that maps to human chromosome 2p22.2. As the second largest human chromosome, chromosome 2 makes up approximately 8% of the human genome and contains 237 million bases encoding over 1,400 genes. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstr syndrome, is related to mutations in the ALMS1 gene. Chromosome 2 contains a probable vestigial second centromere as well as vestigial telomeres, which gives credence to the hypothesis that human chromosome 2 formed as a result of an ancient fusion of two ancestral chromosomes, which are still present in modern day apes.
VE:  1 * 100 µl
Artikel-Nr: (BOSSBS-15154R)

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-15154R
Lokale Artikelnummer:: BOSSBS-15154R
Beschreibung:   C12orf56 (chromosome 12 open reading frame 56), also known as PRO1853 or protein midA homolog, is a 441 amino acid mitochondrial protein that belongs to the midA family. Existing as two alternatively spliced isoforms, C12orf56 is encoded by a gene that maps to human chromosome 2p22.2. As the second largest human chromosome, chromosome 2 makes up approximately 8% of the human genome and contains 237 million bases encoding over 1,400 genes. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstré°‰ syndrome, is related to mutations in the ALMS1 gene. Chromosome 2 contains a probable vestigial second centromere as well as vestigial telomeres, which gives credence to the hypothesis that human chromosome 2 formed as a result of an ancient fusion of two ancestral chromosomes, which are still present in modern day apes.
VE:  1 * 100 µl
Lieferant:  Mettler - Toledo
Beschreibung:   Diese Elektrodenkabel sind für den Anschluss von Mettler-Sensoren an nahezu jedes Messgerät konzipiert.

Lieferant:  OriGene
Hersteller-Artikelnummer:: TA326588
Lokale Artikelnummer:: ORIGTA326588
Beschreibung:   Anti-Slc12a5 Mouse Monoclonal Antibody [clone: S1-12]
VE:  1 * 100 µG
Lieferant:  LGC Standards PROMOCHEM
Hersteller-Artikelnummer:: CIL-EC-4935
Lokale Artikelnummer:: PROOCIL-EC-4935
Beschreibung:   WHO coplanar and mono-ortho PCBs, 1,2 ml in isooctane, : N/A
VE:  1 * 1,2 mL
Lieferant:  ProSci Inc.
Hersteller-Artikelnummer:: 98-557
Lokale Artikelnummer:: PRSI98-557
Beschreibung:   Anti-Cd2 Rat Monoclonal Antibody [clone: 12-15] (PE (Phycoerythrin))
VE:  1 * 0,1 mg
New Product
Lieferant:  SI Analytics
Hersteller-Artikelnummer:: 285215229
Lokale Artikelnummer:: SCOI285215229
Beschreibung:   Tapper adapter, NS 14,5, PTFE, for electrodes with Ø 12 mm
VE:  1 * 1 ST
Lieferant:  Honeywell Chemicals
Hersteller-Artikelnummer:: 16033H-5L
Lokale Artikelnummer:: HONC16033H-5L
Beschreibung:   Propylenglycol ≥99,5%, erfüllt analytische Spezifikationen von BP, Ph. Eur., USP, Riedel-de Haën™
VE:  1 * 5 L
Lieferant:  BIOLEGEND INC
Hersteller-Artikelnummer:: 147605
Lokale Artikelnummer:: BLEG147605
Beschreibung:   Anti-CD100 (SEMA4D) Rat Monoclonal Antibody [clone: BMA-12] (APC (Allophycocyanin))
VE:  1 * 25 µG
Market Source Item This is a MarketSource item. Additional charges may apply

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-11956R-A555
Lokale Artikelnummer:: BOSSBS-11956R-A555
Beschreibung:   The leucine-rich (LRR) repeat is a 20-30 amino acid motif that forms a hydrophobic å/∫ horseshoe fold, allowing it to accommodate several leucine residues within a tightly packed core. All LRR repeats contain a variable segment and a highly conserved segment, the latter of which accounts for 11 or 12 residues of the entire LRR motif. SLITRK3 (SLIT and NTRK-like family, member 3) is a 977 amino acid single-pass type I membrane protein that contains 20 LRR repeats and belongs to the SLITRK family. Expressed at highest levels in cerebral cortex, SLITRK3 is also found in adult and fetal neural tissues and some astrocytic brain tumors. SLITRK3 functions to suppress neurite outgrowth and plays a role in the regulation of neuronal function. SLITRK3 is encoded by a gene that maps to human chromosome 3, which houses over 1,100 genes, including a chemokine receptor (CKR) gene cluster and a variety of human cancer-related gene loci.
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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