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2,2\'-Bipyridin-4,4\'-dicarbonsäure
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2,2\'-Bipyridin-4,4\'-dicarbonsäure
Artikel-Nr:
(BOSSBS-15330R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15330R-FITC
Lokale Artikelnummer::
BOSSBS-15330R-FITC
Beschreibung:
C9orf5 (chromosome 9 open reading frame 5), also known as CG2, is a 911 amino acid multi-pass membrane protein that is widely expressed and exists as four alternatively spliced isoforms. The gene encoding C9orf5 maps to human chromosome 9, which consists of about 145 million bases, represents 4% of the human genome and encodes nearly 900 genes. Considered to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterised by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-15314R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15314R-A488
Lokale Artikelnummer::
BOSSBS-15314R-A488
Beschreibung:
C9orf140 (chromosome 9 open reading frame 140), also known as TS/MDEP (tumor specificity and mitosis phase-dependent expression protein) or p42.3, is a 394 amino acid nuclear and cytoplasmic protein encoded by a gene that maps to human chromosome 9q34.3. Chromosome 9 consists of about 145 million bases, represents 4% of the human genome and encodes nearly 900 genes. Thought to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterised by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias.
VE:
1 * 100 µl
Artikel-Nr:
(1.02092.9025)
Lieferant:
Merck
Hersteller-Artikelnummer::
1.02092.9025
Lokale Artikelnummer::
MERP1.02092.9025
Beschreibung:
tri-Calciumdicitrat Tetrahydrat, EMPROVE® ESSENTIAL DAC, USP, FCC, E333, SAFC®
VE:
1 * 25 kg
Artikel-Nr:
(PRSI2489)
Lieferant:
ProSci Inc.
Hersteller-Artikelnummer::
2489
Lokale Artikelnummer::
PRSI2489
Beschreibung:
IL-22 Receptor Antibody: A novel cytokine, designated IL-TIF for IL-10 related T cell-derived inducible factor and IL-22, was recently identified. The receptor for IL-22 (IL-22R, also termed CRF2-9 and IL-TIF-R1 chain) is a new member of the class II cytokine receptor family. IL-22R forms a complex with IL-10 receptor beta chain and mediates IL-22 signaling. IL-22 and its receptor activate JAK-STAT signaling pathway. IL22R is expressed in normal liver and kidney and their cell lines HepG2 and TK-10. A soluble form of IL-22 receptor, also termed IL-22 binding protein (IL-22BP) and IL-22 receptor-alpha 2 (IL-22RA2), was identified very recently. IL-22BP prevents binding of IL-22 to the functional cell surface IL-22R complex and neutralizes IL-22 activity. LPS induces IL-22 expression, which indicates the role of IL-22 in inflammatory response.
VE:
1 * 100 µG
Artikel-Nr:
(114-9152)
Lieferant:
ATLAS - the shoe company
Hersteller-Artikelnummer::
36700/44
Lokale Artikelnummer::
ATLA36700/44
Beschreibung:
Reinraum-Sicherheitsschuhe mit Cleanline Obermaterial, dem atmungsaktiven active-X® Funktionsinnenfutter und dem ganzheitlichen INNOFLEX Laufsohlensystem, das den Läufer in jeder Bewegungsphase unterstützt.
VE:
1 * 1 PAAR
Artikel-Nr:
(BLEG576209)
Lieferant:
BIOLEGEND INC
Hersteller-Artikelnummer::
576209
Lokale Artikelnummer::
BLEG576209
Beschreibung:
ELISA Standard 4-Pack contains four vials of recombinant mouse IL-22 at >5 ng per vial. Recommended for ELISA application only. Standards are calibrated against a BioLegend Master Calibrator.
VE:
1 * 1 Pack.
 This is a MarketSource item. Additional charges may apply
Artikel-Nr:
(BOSSBS-15350R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15350R-A647
Lokale Artikelnummer::
BOSSBS-15350R-A647
Beschreibung:
C9orf96, also known as Protein kinase-like protein SgK071, is a 680 amino acid protein that belongs to the Ser/Thr protein kinase family of the protein kinase superfamily. There are three isoforms of C9orf96 that are produced as a result of alternative splicing events. The gene encoding C9orf96 maps to human chromosome 9, which consists of about 145 million bases and 4% of the human genome and encodes nearly 900 genes. Considered to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterised by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias.
VE:
1 * 100 µl
Lieferant:
DICKSON
Beschreibung:
Diagramm für Schreiber, C320, +22...+68 °F
Artikel-Nr:
(114-9278)
Lieferant:
ATLAS - the shoe company
Hersteller-Artikelnummer::
49700/44
Lokale Artikelnummer::
ATLA49700/44
Beschreibung:
ESD-Sicherheitsschuh im Sneaker-Style mit Mesh Obermaterial und einer Run 3 Laufsohle aus MPU-Schaum.
VE:
1 * 1 PAAR
Artikel-Nr:
(ELGALA682)
Lieferant:
ELGA LabWater
Hersteller-Artikelnummer::
LA682
Lokale Artikelnummer::
ELGALA682
Beschreibung:
Hygienic sample point, 15 and 22 mm
VE:
1 * 1 ST
Artikel-Nr:
(EHERL20018000IO)
Lieferant:
EHRENSTORFER
Hersteller-Artikelnummer::
L20018000IO
Lokale Artikelnummer::
EHERL20018000IO
Beschreibung:
Organic Standard, 2,2',3,4,4',5,5'-Heptachlorbiphenyl (PCB Nr. 180) 10 µg/ml in Isooctan, Packung: Glasflasche
VE:
1 * 10 mL
Artikel-Nr:
(PRSI34-188)
Lieferant:
ProSci Inc.
Hersteller-Artikelnummer::
34-188
Lokale Artikelnummer::
PRSI34-188
Beschreibung:
CD6 is a type I transmembrane glycoprotein that contains a 24-amino acid signal sequence, three extracellular 'scavenger receptor cysteine-rich' (SRCR) domains, a membrane-spanning domain and a 44-amino acid cytoplasmic domain. The CD6 glycoprotein is tyrosine phosphorylated during TCR-mediated T cell activation. CD6 shows significant homology to CD5. CD6 is present on mature thymocytes, peripheral T cells and a subset of B cells. Antibodies to CD6 are used to deplete T cells from bone marrow transplants to prevent graft versus host disease.
VE:
1 * 100 µG
New Product
Artikel-Nr:
(BLEG835301)
Lieferant:
BIOLEGEND INC
Hersteller-Artikelnummer::
835301
Lokale Artikelnummer::
BLEG835301
Beschreibung:
Anti-GFAP (Cocktail) Mouse Monoclonal Antibody [clone: SMI 22]
VE:
1 * 100 µl
This is a MarketSource item. Additional charges may apply
Artikel-Nr:
(BOSSBS-9748R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9748R-CY3
Lokale Artikelnummer::
BOSSBS-9748R-CY3
Beschreibung:
Ankyrins are membrane adaptor molecules that play important roles in coupling integral membrane proteins to the spectrin-based cytoskeleton network. Mutations of ankyrin genes lead to severe genetic diseases, such as fatal cardiac arrhythmias and hereditary spherocytosis. ANKRD22 (ankyrin repeat domain 22) is a 191 amino acid protein that contains four ANK repeats. Conserved in chimpanzee, dog, cow, mouse, rat, chicken and zebrafish, ANKRD22 is encoded by a gene that maps to human chromosome 10. Chromosome 10 encodes nearly 1,200 genes within 135 million bases, making up approximately 4.5% of the human genome. Several protein-coding genes, including those that encode for chemokines, cadherins, excision repair proteins, early growth response factors (Egrs) and fibroblast growth receptors (FGFRs), are located on chromosome 10. Defects in genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman’s syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-15318R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15318R-A680
Lokale Artikelnummer::
BOSSBS-15318R-A680
Beschreibung:
C9orf169 (chromosome 9 open reading frame 169) is a 423 amino acid single-pass membrane protein that belongs to the clpA/clpB family and torsin subfamily. The gene encoding C9orf169 maps to human chromosome 9q34.3. Chromosome 9 consists of about 145 million bases, represents 4% of the human genome and encodes nearly 900 genes. Thought to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterised by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9747R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9747R-A488
Lokale Artikelnummer::
BOSSBS-9747R-A488
Beschreibung:
Ankyrins are membrane adaptor molecules that play important roles in coupling integral membrane proteins to the spectrin-based cytoskeleton network. Mutations of ankyrin genes lead to severe genetic diseases such as fatal cardiac arrhythmias and hereditary spherocytosis. ANKRD20A (ankyrin repeat domain-containing protein 20A) is an 823 amino acid protein that contains five ANK repeats. The gene encoding ANKRD20A maps to chromosome 9, which consists of about 145 million bases and encodes nearly 900 genes. Considered to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, and familial dysautonomia are associated with chromosome 9. Also, chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in 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.
Dieses Produkt kann nur an eine Lieferadresse versandt werden die über die entsprechende Lizenzen verfügt. Für weitere Hilfe bitte kontaktieren Sie Ihr VWR Vertriebszentrum.
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