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2,2\',4,5-Tetrachlorbiphenyl+(PCB+Nr.+48)
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2,2\',4,5-Tetrachlorbiphenyl+(PCB+Nr.+48)
Artikel-Nr:
(BOSSBS-11034R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11034R-A680
Lokale Artikelnummer::
BOSSBS-11034R-A680
Beschreibung:
MYBPC1 is a 1141 amino acid protein that contains three fibronectin type-III domains and seven Ig-like C2-type domains. Existing as a member of the immunoglobulin superfamily, MYBPC1 functions as a thick filament-associated protein that localizes to striated muscle bands in vertebrae and is thought to modify the activity of select ATPases. Additionally, MYBPC1 may play a role in the modulation of muscle contraction and in the overall structural integrity of the cell. The gene encoding MYBPC1 maps to human chromosome 12, which encodes over 1100 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
Artikel-Nr:
(BOSSBS-8302R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8302R-A647
Lokale Artikelnummer::
BOSSBS-8302R-A647
Beschreibung:
GLT8D2 (glycosyltransferase 8 domain-containing protein 2), also known as GALA4A, is a 349 amino acid single-pass type II membrane protein. A member of the glycosyltransferase 8 family, GLT8D2 is encoded by a gene that maps to human chromosome 12q23.3. Encoding over 1,100 genes within 132 million base pairs, chromosome 12 makes up about 4.5% of the human genome. A number of skeletal deformities are linked to chromosome 12, including hypochondrogenesis, achondrogenesis, Noonan syndrome, Kniest dysplasia and trisomy 12p. Chromosome 12 is also home to a homeobox gene cluster, which encodes crucial transcription factors for morphogenesis, as well as the natural killer complex gene cluster, which encodes C-type lectin proteins that mediate the NK cell response to MHC I interaction.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9720R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9720R-A750
Lokale Artikelnummer::
BOSSBS-9720R-A750
Beschreibung:
C10orf27, also known as spatial, is a 351 amino acid cytoplasmic protein belonging to the spatial family. C10orf27 is suggested to play a role in spermatid differentiation. Existing as two alternatively spliced isoforms, C10orf27 is widely expressed in multiple tissues, including brain, thymus and testis. C10orf27 may be associated with multiple sclerosis (MS) susceptibility and pathogenesis. MS is an inflammatory disease that causes gradual destruction of myelin in the central nervous system. C10orf27 is encoded by a gene located on human chromosome 10, which contains over 800 genes and 135 million nucleotides, making up nearly 4.5% of the human genome. PTEN is an important tumour suppressor gene located on chromosome 10 and, when defective, causes a genetic predisposition to cancer development known as Cowden syndrome.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8302R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8302R-CY3
Lokale Artikelnummer::
BOSSBS-8302R-CY3
Beschreibung:
GLT8D2 (glycosyltransferase 8 domain-containing protein 2), also known as GALA4A, is a 349 amino acid single-pass type II membrane protein. A member of the glycosyltransferase 8 family, GLT8D2 is encoded by a gene that maps to human chromosome 12q23.3. Encoding over 1,100 genes within 132 million base pairs, chromosome 12 makes up about 4.5% of the human genome. A number of skeletal deformities are linked to chromosome 12, including hypochondrogenesis, achondrogenesis, Noonan syndrome, Kniest dysplasia and trisomy 12p. Chromosome 12 is also home to a homeobox gene cluster, which encodes crucial transcription factors for morphogenesis, as well as the natural killer complex gene cluster, which encodes C-type lectin proteins that mediate the NK cell response to MHC I interaction.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8302R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8302R
Lokale Artikelnummer::
BOSSBS-8302R
Beschreibung:
GLT8D2 (glycosyltransferase 8 domain-containing protein 2), also known as GALA4A, is a 349 amino acid single-pass type II membrane protein. A member of the glycosyltransferase 8 family, GLT8D2 is encoded by a gene that maps to human chromosome 12q23.3. Encoding over 1,100 genes within 132 million base pairs, chromosome 12 makes up about 4.5% of the human genome. A number of skeletal deformities are linked to chromosome 12, including hypochondrogenesis, achondrogenesis, Noonan syndrome, Kniest dysplasia and trisomy 12p. Chromosome 12 is also home to a homeobox gene cluster, which encodes crucial transcription factors for morphogenesis, as well as the natural killer complex gene cluster, which encodes C-type lectin proteins that mediate the NK cell response to MHC I interaction.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8302R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8302R-A555
Lokale Artikelnummer::
BOSSBS-8302R-A555
Beschreibung:
GLT8D2 (glycosyltransferase 8 domain-containing protein 2), also known as GALA4A, is a 349 amino acid single-pass type II membrane protein. A member of the glycosyltransferase 8 family, GLT8D2 is encoded by a gene that maps to human chromosome 12q23.3. Encoding over 1,100 genes within 132 million base pairs, chromosome 12 makes up about 4.5% of the human genome. A number of skeletal deformities are linked to chromosome 12, including hypochondrogenesis, achondrogenesis, Noonan syndrome, Kniest dysplasia and trisomy 12p. Chromosome 12 is also home to a homeobox gene cluster, which encodes crucial transcription factors for morphogenesis, as well as the natural killer complex gene cluster, which encodes C-type lectin proteins that mediate the NK cell response to MHC I interaction.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8579R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8579R-A750
Lokale Artikelnummer::
BOSSBS-8579R-A750
Beschreibung:
The finding that mutations in DNA mismatch repair genes are associated with hereditary nonpolyposis colorectal cancer (HNPCC) has resulted in considerable interest in the understanding of the mechanism of DNA mismatch repair. Initially, inherited mutations in the MSH2 and MLH1 homologs of the bacterial DNA mismatch repair genes MutS and MutL were demonstrated at high frequency in HNPCC and were shown to be associated with microsatellite instability. The demonstration that 10 to 45% of pancreatic, gastric, breast, ovarian and small cell lung cancers also display microsatellite instability has been interpreted to suggest that DNA mismatch repair is not restricted to HNPCC tumors but is a common feature in tumor initiation or progression. Two additional homologs of the prokaryotic MutL gene, designated PMS1 and PMS2, have been identified and shown to be mutated in the germline of HNPCC patients.
VE:
1 * 100 µl
Artikel-Nr:
(ABCRAB108361.0001)
Lieferant:
ABCR
Hersteller-Artikelnummer::
AB108361.0001
Lokale Artikelnummer::
ABCRAB108361.0001
Beschreibung:
4-Fluor-2-(trifluormethyl)benzylbromid
VE:
1 * 1 g
 This is a MarketSource item. Additional charges may apply
Lieferant:
Thermo Scientific
Beschreibung:
EDTA Magnesiumdikaliumsalz 97%
Lieferant:
BIOLEGEND INC
Beschreibung:
Anti-HMB-45 Mouse Monoclonal Antibody [clone: HMB-45] (Alexa Fluor® 647)
Artikel-Nr:
(BOSSBS-8870R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8870R-A680
Lokale Artikelnummer::
BOSSBS-8870R-A680
Beschreibung:
The product encoded by this gene is involved in the maintenance of iron homeostasis, and it is necessary for the regulation of iron storage in macrophages, and for intestinal iron absorption. The preproprotein is post-translationally cleaved into mature peptides of 20, 22 and 25 amino acids, and these active peptides are rich in cysteines, which form intramolecular bonds that stabilise their beta-sheet structures. These peptides exhibit antimicrobial activity. Mutations in this gene cause hemochromatosis type 2B, also known as juvenile hemochromatosis, a disease caused by severe iron overload that results in cardiomyopathy, cirrhosis, and endocrine failure.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8870R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8870R-A750
Lokale Artikelnummer::
BOSSBS-8870R-A750
Beschreibung:
The product encoded by this gene is involved in the maintenance of iron homeostasis, and it is necessary for the regulation of iron storage in macrophages, and for intestinal iron absorption. The preproprotein is post-translationally cleaved into mature peptides of 20, 22 and 25 amino acids, and these active peptides are rich in cysteines, which form intramolecular bonds that stabilise their beta-sheet structures. These peptides exhibit antimicrobial activity. Mutations in this gene cause hemochromatosis type 2B, also known as juvenile hemochromatosis, a disease caused by severe iron overload that results in cardiomyopathy, cirrhosis, and endocrine failure.
VE:
1 * 100 µl
Artikel-Nr:
(BLDPBD18297-500G)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD18297-500G
Lokale Artikelnummer::
BLDPBD18297-500G
Beschreibung:
D(-)-N-Ethylglucamin 98%
VE:
1 * 500 g
Lieferant:
Sigma-Aldrich
Beschreibung:
Phenylvinylsulfon, Sigma-Aldrich®
Lieferant:
Portwest Clothing
Beschreibung:
Upmarket range of everyday safety footwear at an affordable price. Eye catching design with orange trims and full safety specification with steel toecap and midsole, antistatic and slip resistant.
Artikel-Nr:
(10050.)
Lieferant:
Biotium
Hersteller-Artikelnummer::
10050
Lokale Artikelnummer::
BTIU10050
Beschreibung:
ABTS (Diammonium-2,2'-azinobis[3-ethyl-2,3-dihydrobenzothiazol-6-sulfonat])
VE:
1 * 1 g
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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