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Methyl+3-amino-7-fluorobenzo[b]thiophene-2-carboxylate
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Methyl+3-amino-7-fluorobenzo[b]thiophene-2-carboxylate
Artikel-Nr:
(APOSBIM0197-500G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
BIM0197-500G
Lokale Artikelnummer::
APOSBIM0197-500G
Beschreibung:
MOPS-Na ≥98%
VE:
1 * 500 g
Artikel-Nr:
(BOSSBS-13747R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13747R-CY7
Lokale Artikelnummer::
BOSSBS-13747R-CY7
Beschreibung:
The claudin superfamily consists of many structurally related proteins that are important structural and functional components of tight junctions in paracellular transport. Claudins are located in both epithelial and endothelial cells in all tight junction-bearing tissues. Claudins, which consist of four transmembrane domains and two extracellular loops, make up tight junction strands. It is suggested that the claudin family of proteins regulate transport through tight junctions via differential discrimination for solute size and charge. Claudin expression is often highly restricted to specific regions of different tissues and may have an important role in transcellular transport through tight junctions. Claudin-22, also known as CLDN22, is a 220 amino acid member of the claudin family that participates in tight junction-specific obliteration of the intercellular space through calcium-independent cell-adhesion activity.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9369R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9369R-A647
Lokale Artikelnummer::
BOSSBS-9369R-A647
Beschreibung:
ODF3B, also known as ODF3L3 (outer dense fiber protein 3-like protein 3), is a 253 amino acid protein belonging to the ODF3 family. Existing as two isoforms produced by alternative splicing, ODF3B contains one DUF1309 repeat. The gene that encodes ODF3B maps to human chromosome 22, which contains over 500 genes and about 49 million bases. Being the second smallest human chromosome, 22 contains a surprising variety of interesting genes. Phelan-McDermid syndrome, Neurofibromatosis type 2 and autism are associated with chromosome 22. A schizophrenia susceptibility locus has been identified on chromosome 22 and studies show that 22q11 deletion symptoms include a high incidence of schizophrenia. Translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia Chromosome and the subsequent production of the novel fusion protein, BCR-Abl, a potent cell proliferation activator found in several types of leukemia.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-1724R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-1724R
Lokale Artikelnummer::
BOSSBS-1724R
Beschreibung:
Motilin is a 22 amino acid peptide hormone expressed throughout the gastrointestinal (GI) tract. The protein encoded by this gene is a motilin receptor which is a member of the G-protein coupled receptor 1 family. This member is a multi-pass transmembrane protein, and is an important therapeutic target for the treatment of hypomotility disorders.
VE:
1 * 100 µl
Artikel-Nr:
(ROCK600-403-466)
Lieferant:
Rockland Immunochemicals
Hersteller-Artikelnummer::
600-403-466
Lokale Artikelnummer::
ROCK600-403-466
Beschreibung:
Anti-KLH Antibody Peroxidase Conjugated antibody has been assayed against 1.0 µg of KLH in a standard capture ELISA using ABTS (2,2’-azino-bis-(3-ethylbenthiazoline-6-sulfonic acid)) substrate for 30 minutes at room temperature.
VE:
1 * 100 µG
Artikel-Nr:
(ROCK601-4602)
Lieferant:
Rockland Immunochemicals
Hersteller-Artikelnummer::
601-4602
Lokale Artikelnummer::
ROCK601-4602
Beschreibung:
Anti-Bovine IgG (H&L) has been assayed against 1.0 µg of Bovine IgG in a standard capture ELISA using Peroxidase Conjugated Streptavidin and ABTS (2,2’-azino-bis-(3-ethylbenthiazoline-6-sulfonic acid)) as a substrate for 30 minutes at room temperature.
VE:
1 * 2 mg
Artikel-Nr:
(ROCK616-1602)
Lieferant:
Rockland Immunochemicals
Hersteller-Artikelnummer::
616-1602
Lokale Artikelnummer::
ROCK616-1602
Beschreibung:
Anti-Donkey IgG (H&L) has been assayed against 1.0 µg of Donkey IgG in a standard capture ELISA using Peroxidase Conjugated Streptavidin and ABTS (2,2’-azino-bis-(3-ethylbenthiazoline-6-sulfonic acid)) as a substrate for 30 minutes at room temperature.
VE:
1 * 2 mg
Artikel-Nr:
(BOSSBS-9985R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9985R-A750
Lokale Artikelnummer::
BOSSBS-9985R-A750
Beschreibung:
HSPC117, also known as C22orf28, is a 505 amino acid protein that is encoded by a gene which maps to human chromosome 22. A highly homologous protein identified in rodents, FAAP (focal adhesion associated protein), encoded by murine D10Wsu52e gene, has been suggested to play a role in regulating cell adhesion dynamics. Chromosome 22 houses over 500 genes and is the second smallest human chromosome. Mutations in several of the genes that map to chromosome 22 are involved in the development of Phelan-McDermid syndrome, Neurofibromatosis type 2, autism and schizophrenia. Additionally, translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia Chromosome and the subsequent production of the novel fusion protein BCR-Abl, a potent cell proliferation activator found in several types of leukaemias.
VE:
1 * 100 µl
Lieferant:
Thermo Scientific
Beschreibung:
CAS No.: 194491-31-1
Artikel-Nr:
(BOSSBS-13747R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13747R-A488
Lokale Artikelnummer::
BOSSBS-13747R-A488
Beschreibung:
The claudin superfamily consists of many structurally related proteins that are important structural and functional components of tight junctions in paracellular transport. Claudins are located in both epithelial and endothelial cells in all tight junction-bearing tissues. Claudins, which consist of four transmembrane domains and two extracellular loops, make up tight junction strands. It is suggested that the claudin family of proteins regulate transport through tight junctions via differential discrimination for solute size and charge. Claudin expression is often highly restricted to specific regions of different tissues and may have an important role in transcellular transport through tight junctions. Claudin-22, also known as CLDN22, is a 220 amino acid member of the claudin family that participates in tight junction-specific obliteration of the intercellular space through calcium-independent cell-adhesion activity.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13747R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13747R-A750
Lokale Artikelnummer::
BOSSBS-13747R-A750
Beschreibung:
The claudin superfamily consists of many structurally related proteins that are important structural and functional components of tight junctions in paracellular transport. Claudins are located in both epithelial and endothelial cells in all tight junction-bearing tissues. Claudins, which consist of four transmembrane domains and two extracellular loops, make up tight junction strands. It is suggested that the claudin family of proteins regulate transport through tight junctions via differential discrimination for solute size and charge. Claudin expression is often highly restricted to specific regions of different tissues and may have an important role in transcellular transport through tight junctions. Claudin-22, also known as CLDN22, is a 220 amino acid member of the claudin family that participates in tight junction-specific obliteration of the intercellular space through calcium-independent cell-adhesion activity.
VE:
1 * 100 µl
Artikel-Nr:
(26086.103)
Lieferant:
VWR Chemicals
Lokale Artikelnummer::
VWRC26086.103
Beschreibung:
Xylenolorange Tetranatriumsalz, TECHNICAL
VE:
1 * 5 g
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
USP, pyrogen free.
Artikel-Nr:
(BOSSBS-6406R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-6406R-A488
Lokale Artikelnummer::
BOSSBS-6406R-A488
Beschreibung:
CESK1, also known as CCT8L2 (chaperonin containing TCP1, subunit 8 theta-like 2), is a 557 amino acid protein that localizes to the cytoplasm and is thought to function as a molecular chaperone, possibly assisting protein folding after ATP hydrolysis. CESK1 belongs to the TCP-1 chaperonin family and is encoded by a gene which maps to human chromosome 22. Mutations in several of the genes that map to chromosome 22 are involved in the development of Phelan-McDermid syndrome, neurofibromatosis type 2, autism and schizophrenia. Additionally, translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia chromosome and the subsequent production of the novel fusion protein Bcr-Abl, a potent cell proliferation activator found in several types of leukemias.
VE:
1 * 100 µl
Artikel-Nr:
(APOSBISN0100-5MG)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
BISN0100-5MG
Lokale Artikelnummer::
APOSBISN0100-5MG
Beschreibung:
Delamanid a mycobacterial cell wall synthesis inhibitor inhibits the synthesisi of mucolic acids cruciala component of the cell wall of the Mycobacterium tuberculosis complex.
VE:
1 * 5 mg
Artikel-Nr:
(BOSSBS-11489R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11489R-CY5
Lokale Artikelnummer::
BOSSBS-11489R-CY5
Beschreibung:
TNRC6B is a 1,723 amino acid protein that exists as two alternatively spliced isoforms and is thought to be involved in mRNA cleavage events. Expressed ubiquitously, TNRC6B contains one glycine/tryptophan (GW)-rich N-terminal domain, one central glutamine-rich region and one C-terminal RNA recognition motif and is encoded by a gene that maps to human chromosome 22. Mutations in several of the genes that map to chromosome 22 are involved in the development of Phelan-McDermid syndrome, Neurofibromatosis type 2, autism and schizophrenia. Additionally, translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia Chromosome and the subsequent production of the novel fusion protein BCR-Abl, a potent cell proliferation activator found in several types of leukemias.
VE:
1 * 100 µl
Preis auf Anfrage
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 noch angezeigt wird und Sie Hilfe benötigen, rufen Sie uns an 1-800-932 - 5000.
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
noch angezeigt wird und Sie Hilfe benötigen, rufen Sie uns an 1-800-932 - 5000.
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