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7-Chlorothieno[3,2-b]pyridine-6-carbonitrile
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7-Chlorothieno[3,2-b]pyridine-6-carbonitrile
Artikel-Nr:
(BOSSBS-3672R-CY5.5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-3672R-CY5.5
Lokale Artikelnummer::
BOSSBS-3672R-CY5.5
Beschreibung:
Hsp22 (HSPB8) is a 196-amino acid protein that contains a central portion homologous to a highly conserved HSP-alpha crystallin domain common to all the small heat shock protein (HSP20) family members. Hsp22 is a monomeric protein which interacts with HSPB1. It displays temperature-dependent chaperone activity. The highest abundance of Hsp22 is in skeletal muscle, heart, and placenta. Mutations in the HSPB8 gene are associated with the inherited peripheral neuropathies, autosomal dominant distal hereditary motor neuropathy type IIA (dSMA) and axonal Charcot-Marie-Tooth disease type 2L (CMT2L).
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-12490R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12490R-A350
Lokale Artikelnummer::
BOSSBS-12490R-A350
Beschreibung:
APMAP is a 416 amino acid single-pass type II membrane protein that belongs to the strictosidine synthase family and is thought to play a role in adipocyte differentiation. The gene encoding C20orf3 maps to human chromosome 20, which houses over 600 genes some of which are associated with Creutzfeldt-Jakob disease, amyotrophic lateral sclerosis, spinal muscular atrophy, ring chromosome 20 epilepsy syndrome and Alagille syndrome. Additionally, chromosome 20 contains a region with numerous genes which are thought important for seminal production and may be potential targets for male contraception.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8112R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8112R-A488
Lokale Artikelnummer::
BOSSBS-8112R-A488
Beschreibung:
CCDC117 is a 279 amino acid protein that is expressed as multiple alternatively spliced isoforms and is encoded by a gene which maps to human chromosome 22. 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 leukemias.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8112R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8112R-A750
Lokale Artikelnummer::
BOSSBS-8112R-A750
Beschreibung:
CCDC117 is a 279 amino acid protein that is expressed as multiple alternatively spliced isoforms and is encoded by a gene which maps to human chromosome 22. 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 leukemias.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9991R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9991R-A680
Lokale Artikelnummer::
BOSSBS-9991R-A680
Beschreibung:
C4orf22 is a 233 amino acid protein that exists as three alternatively spliced isoforms and are encoded by a gene encoding maping to human chromosome 4, which represents approximately 6% of the human genome and contains nearly 900 genes. Notably, the Huntingtin gene, which is found to encode an expanded glutamine tract in cases of Huntington's disease, is on chromosome 4. FGFR-3 is also encoded by a gene that maps to chromosome 4 and has been associated with thanatophoric dwarfism, achondroplasia, Muenke syndrome and bladder cancer. Chromosome 4 is also tied to Ellis-van Creveld syndrome, methylmalonic acidemia and polycystic kidney disease.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9635R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9635R-CY5
Lokale Artikelnummer::
BOSSBS-9635R-CY5
Beschreibung:
Zinc is an essential cofactor that is involved in cell growth and development, as well as in protein, nucleic acid and lipid metabolism. The transport of zinc across the cell membrane is crucial for correct enzyme and overall cell function. SLC39A11 (solute carrier family 39 (metal ion transporter), member 11), also known as ZIP11 (Zrt- and Irt-like protein 11), is a 342 amino acid multi-pass membrane protein belonging to the ZIP transporter family. Expressed as multiple alternatively spliced isoforms, SLC39A11 acts as a zinc-influx transporter and is encoded by a gene located on human chromosome 17, which comprises over 2.5% of the human genome and encodes over 1,200 genes, some of which are involved in tumor suppression and in the pathogenesis of Li-Fraumeni syndrome, early onset breast cancer and a predisposition to cancers of the ovary, colon, prostate gland and fallopian tubes.
VE:
1 * 100 µl
Artikel-Nr:
(SIAL09793-1G)
Lieferant:
Sigma-Aldrich
Hersteller-Artikelnummer::
09793-1G
Lokale Artikelnummer::
SIAL09793-1G
Beschreibung:
(S)-3-(Boc-amino)-3-phenylpropionsäure, Sigma-Aldrich®
VE:
1 * 1 g
Artikel-Nr:
(COBBPN-8365-1G)
Lieferant:
COMBI-BLOCKS
Hersteller-Artikelnummer::
PN-8365-1G
Lokale Artikelnummer::
COBBPN-8365-1G
Beschreibung:
3-Amino-4-fluorphenylboronsäurepinakolester
VE:
1 * 1 g
 This is a MarketSource item. Additional charges may apply
Artikel-Nr:
(203783-100)
Lieferant:
Merck Millipore (Calbiochem)
Hersteller-Artikelnummer::
203783-100
Lokale Artikelnummer::
CALB203783-100
Beschreibung:
X-Gluc (5-Brom-4-chlor-3-indolyl-ß-D-glucuronid Cyclohexylammoniumsalz, X-GlcA), Sigma-Aldrich®
VE:
1 * 100 mg
Artikel-Nr:
(BOSSBS-8152R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8152R
Lokale Artikelnummer::
BOSSBS-8152R
Beschreibung:
FAM50A, also known as DXS9928E, HXC26, XAP5 or 9F, is a 339 amino acid nuclear protein that belongs to the FAM50 family. Expressed ubiquitously with highest expression in fetal kidney, liver and brain, as well as adult heart, spleen, skeletal muscle, prostate and small intestine, FAM50A is thought to function as a transcription factor that may bind to DNA. FAM50A contains an SV40 large T antigen nuclear localization signal and a polymorphic CCG repeat region in its 5’-UTR. Defects in the gene encoding FAM50A may be associated with acute lymphoblastic leukemia, suggesting a possible role for FAM50A in carcinogenesis.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-12324R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12324R-CY5
Lokale Artikelnummer::
BOSSBS-12324R-CY5
Beschreibung:
PTCHD2 is a 1,392 amino acid multi-pass membrane protein that contains one SSD (sterol-sensing) domain and belongs to the patched family. Expressed in retina, brain and testis, PTCHD2 localizes to endoplasmic reticulum and colocalizes with cholesterol. PTCHD2 overexpression leads to increased cholesterol levels, suggesting that PTCHD2 may play a role in cholesterol homeostasis. PTCHD2 is further hypothesized to act as a link between thyroid hormone and cholesterol metabolism. Existing as two alternatively spliced isoforms, PTCHD2 is thought to assist in the release of lipid-anchored secreted proteins and is encoded by a gene that maps to human chromosome 1p36.22.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13043R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13043R-CY7
Lokale Artikelnummer::
BOSSBS-13043R-CY7
Beschreibung:
The gene encoding DYX1C1 maps in the 15q21 region, which is disrupted by a translocation t(2;15)(q11;q21) and segregates with dyslexia. Two sequence changes in DYX1C1, including one involving the translation initiation sequence and an Elk-1 transcription factor binding site (-3G -->A) and a codon (1249G -->T), introduce a premature stop codon and truncate the protein by 4 amino acids. DYX1C1 encodes a nuclear tetratricopeptide repeat domain protein that is dynamically regulated in brain. In human brain, DYX1C1 protein localizes to a fraction of cortical neurons and white matter glial cells. It is also expressed in lung, kidney and testis.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-1012R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-1012R-CY5
Lokale Artikelnummer::
BOSSBS-1012R-CY5
Beschreibung:
BMP2 belongs to the transforming growth factor-beta (TGFB) superfamily of secreted growth factors. It is a disulfide-linked homodimer and induces bone and cartilage formation. In addition to its osteogenic activity, BMP2 plays an important role in cardiac morphogenesis and is expressed in a variety of tissues including lung, spleen, brain, liver, prostate ovary and small intestine. The functional form of BMP2 is a 26 kDa protein composed of two identical 114 amino acid polypeptide chains linked by a single disulfide bond. BMPs control fundamental events in early embryonic development, organogenesis and adult tissue homeostasis.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13479R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13479R-CY7
Lokale Artikelnummer::
BOSSBS-13479R-CY7
Beschreibung:
GNS is a 552 amino acid lysosomal enzyme that hydrolyzes the 6-sulfate groups of the N-acetyl-D-glucosamine 6-sulfate units of keratan sulfate and heparan sulfate. A member of the sulfatase family, GNS assists in the catabolism of heparin, and binds calcium as a cofactor. GNS deficiency results in an autosomal recessive lysosomal storage disorder known as mucopolysaccharidosis type IIID (Sanfilippo D syndrome), which is characterized by mild somatic disease and severe degeneration of the central nervous system. Subject to post-translational internal peptidase cleavage, GNS is encoded by a gene mapping to human chromosome 12q14.2 and mouse chromosome 10 D2.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9098R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9098R
Lokale Artikelnummer::
BOSSBS-9098R
Beschreibung:
ANKS3 is a 656 amino acid protein that contain six ANK repeats and one SAM (sterile alpha motif) domain. The gene encoding ANKS3 maps to human chromosome 16. Chromosome 16, which is associated with a variety of genetic disorders, encodes over 900 genes and comprises nearly 3% of the human genome. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is associated with chromosome 16, as is Crohn's disease, which is a gastrointestinal inflammatory condition.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11841R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11841R-CY7
Lokale Artikelnummer::
BOSSBS-11841R-CY7
Beschreibung:
TOCA-1 is a 605 amino acid protein that localizes to the cytoplasm and the cytoskeleton, as well as to cytoplasmic vesicles and the cell membrane, and contains one FCH domain, one REM repeat and one SH3 domain. Existing as multiple alternatively spliced isoforms, TOCA-1 interacts with CDC42 and is required for the coordination of membrane tubulation with Actin cytoskeletal reorganization during endocytosis. Additionally, TOCA-1 is involved in membrane invagination, tubule formation and Actin polymerization. The gene encoding TOCA-1 maps to human chromosome 1, which spans 260 million base pairs, contains over 3,000 genes and comprises nearly 8% of the human genome.
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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