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b-Amino-4-bromobenzeneethanol


159 979  results were found

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Artikel-Nr: (EHERC11201000)

Lieferant:  EHRENSTORFER
Hersteller-Artikelnummer:: C11201000
Lokale Artikelnummer:: EHERC11201000
Beschreibung:   cis-Chlordan
VE:  1 * 10 mg
Artikel-Nr: (EHERC15990100)

Lieferant:  EHRENSTORFER
Hersteller-Artikelnummer:: C15990100
Lokale Artikelnummer:: EHERC15990100
Beschreibung:   cis-Permethrin
VE:  1 * 10 mg

Lieferant:  COMBI-BLOCKS
Hersteller-Artikelnummer:: PN-6028-1G
Lokale Artikelnummer:: COBBPN-6028-1G
Beschreibung:   2-Amino-4-(trifluormethoxy)phenylboronsäurepinakolester
VE:  1 * 1 g
Market Source Item This is a MarketSource item. Additional charges may apply
Lieferant:  APOLLO SCIENTIFIC
Beschreibung:   Citraconsäure 95%
Lieferant:  COMBI-BLOCKS
Beschreibung:   2-(Cbz-amino)-5-pyrimidinboronsäurepinakolester
Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-13125R-HRP
Lokale Artikelnummer:: BOSSBS-13125R-HRP
Beschreibung:   A gene on chromosome 20q13.1 encodes Eya2 (eyes absent). EYA2 is one of four members of the eyes absent family. A 271 amino acid domain at the carboxy-terminal is highly conserved amongst the members of the eyes absent family, while the PST (proline-serive-threonin)-rich amino-terminal is highly divergent. EYA2 is expressed relatively late in development in the cytoplasm of extensor tendons and ligaments of the phalangeal elements of the limb, cranial placodes, branchial arches, central nervous system, and the developing eye. Pax3 induces the expression of Eya2 in a cascade that is necessary and sufficient for myogenesis. EYA2, like EYA1, acts as a transcriptional activator in connective tissue patterning through its PST domain, which functions as a transactivation domain. EYA2 is translocated to the nucleus by Six proteins, which interact through their domain and homeodomain with EYA2. EYA2 carboxy-terminal interacts with the G Alpha z and G Alphai 2 proteins. This interaction prevents Six proteins from translocating EYA2 to the nucleus.
VE:  1 * 100 µl
Lieferant:  BIONET RESEARCH
Beschreibung:   3-Amino-3-(3,4-dichlorphenyl)propionsäure
Lieferant:  Biotium
Hersteller-Artikelnummer:: BNUM0337-50
Lokale Artikelnummer:: BTIUBNUM0337-50
Beschreibung:   CD98 exits as a heterodimer containing a disulphide-linked glycosylated heavy chain and a non-glycosylated light chain. It is a member of the solute carrier family and encodes a cell surface, transmembrane protein. The protein exists as the heavy chain of a heterodimer, covalently bound through disulfide bonds to one of several possible light chains. The encoded transporter plays a role in regulation of intracellular calcium levels and transports L-type amino acids. Alternatively spliced transcript variants, encoding different isoforms, have been characterized.
VE:  1 * 50 µl
Lieferant:  BIONET RESEARCH
Beschreibung:   3-Amino-3-(4-bromphenyl)propionsäure
Lieferant:  Sigma-Aldrich
Beschreibung:   It contains synthetic α-tocopherol as stabiliser.
Lieferant:  APOLLO SCIENTIFIC
Beschreibung:   Penicillin G is an inhibitor of bacterial cell wall synthesis.Active against gram-positive and some gram-negative bacteria. b-lactamase sensitive.
Artikel-Nr: (BOSSBS-11822R-CY5)

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-11822R-CY5
Lokale Artikelnummer:: BOSSBS-11822R-CY5
Beschreibung:   CSAD is a 493 amino acid protein that exists as a homodimer and belongs to the group II decarboxylase family. CSAD catalyzes the conversion of 3-sulfino-L-alanine to hypotaurine and carbon dioxide, binds pyridoxal phosphate as a cofactor and undergoes alternative splicing to produce three isoforms. The gene encoding CSAD maps to human chromosome 12, which encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders.
VE:  1 * 100 µl
Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-11802R-A680
Lokale Artikelnummer:: BOSSBS-11802R-A680
Beschreibung:   The organic anion transporter family of proteins mediate hepatic uptake of cardiac glycosides. OATP-D is a 710 amino acid member of the organic anion transporter protein family. As a multi-pass membrane protein, OATP-D mediates the Na+-independent transport of vasopressin, prostaglandins (PG) E1 and E2, thyroxine (T4), deltorphin II and other organic anions, but not estrone-3-sulfate, DPDPE, taurocholate, DHEAS or digoxin. OATP-D is ubiquitously expressed with highest levels present in leukocytes and spleen. OATP-D is expressed as four isoforms produced by alternative splicing events.
VE:  1 * 100 µl
Lieferant:  Biotium
Beschreibung:   MAb VU-2G7 reacts with MUC1, a large transmembrane glycoprotein expressed on the ductal surface of normal glandular epithelia. The dominant epitope of VU-2G7 has not been established with epitope fingerprinting. The extracellular domain of MUC1 largely consists of a highly conserved, O-glycosylated 20 amino acids tandem repeat which can occur 30-100 times per molecule depending on the length of the allele involved. In the vast majority of human carcinomas this protein is up regulated and poorly glycosylated and appears on the cell surface in a non-polarized fashion.
Lieferant:  Biotium
Beschreibung:   MAb VU-2G7 reacts with MUC1, a large transmembrane glycoprotein expressed on the ductal surface of normal glandular epithelia. The dominant epitope of VU-2G7 has not been established with epitope fingerprinting. The extracellular domain of MUC1 largely consists of a highly conserved, O-glycosylated 20 amino acids tandem repeat which can occur 30-100 times per molecule depending on the length of the allele involved. In the vast majority of human carcinomas this protein is up regulated and poorly glycosylated and appears on the cell surface in a non-polarized fashion.

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-11822R-A488
Lokale Artikelnummer:: BOSSBS-11822R-A488
Beschreibung:   CSAD is a 493 amino acid protein that exists as a homodimer and belongs to the group II decarboxylase family. CSAD catalyzes the conversion of 3-sulfino-L-alanine to hypotaurine and carbon dioxide, binds pyridoxal phosphate as a cofactor and undergoes alternative splicing to produce three isoforms. The gene encoding CSAD maps to human chromosome 12, which encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders.
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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