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2,2\'-Dihydroxybiphenyl
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2,2\'-Dihydroxybiphenyl
Lieferant:
Borer Chemie
Beschreibung:
Flüssiges, alkalisches Reinigungskonzentrat zur maschinellen Reinigung von Laborglas und wiederverwendbaren Labormaterialien
Artikel-Nr:
(BOSSBS-9174R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9174R-A488
Lokale Artikelnummer::
BOSSBS-9174R-A488
Beschreibung:
Tripartite motif-containing protein 3 (TRIM3), also known as RING finger protein 22 (RNF22), RING finger protein 97 (RNF97) or brain-expressed RING finger protein (BERP), is a 744 amino acid member of the TRIM family, also known as the RING-B-box coiled-coil (RBCC) family. Members of the RBCC family have an N-terminal RING finger, followed by one or two zinc-binding domains (B-box domains), a leucine coiled-coil region and a variable C-terminal domain. Localized to cytoplasmic filaments, TRIM3 has been shown to interact with å-actinin-4 and myosin V, two proteins associated with the actin cytoskeleton. Specifically, å-actinin-4 interacts with the RBCC domain of TRIM3, and the C-terminal tail of Myosin V interacts with with the unique C-terminal ∫-propeller domain of TRIM3. These associations suggest that TRIM3 may play a role in cell motility and cargo transport. Three named isoforms of TRIM3 exist as a result of alternative splicing events.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-15318R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15318R-A350
Lokale Artikelnummer::
BOSSBS-15318R-A350
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-15314R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15314R-A680
Lokale Artikelnummer::
BOSSBS-15314R-A680
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:
(BOSSBS-15314R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15314R-CY7
Lokale Artikelnummer::
BOSSBS-15314R-CY7
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:
(BOSSBS-15314R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15314R-CY3
Lokale Artikelnummer::
BOSSBS-15314R-CY3
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
Lieferant:
SOCOREX ISBA
Beschreibung:
Blunt end cannulas provide precise distribution with Luer nozzle microdispensers.
Lieferant:
Sigma-Aldrich
Beschreibung:
Triethylenglycol, Sigma-Aldrich®
Artikel-Nr:
(MOLE17211839-100G)
Lieferant:
Molekula
Hersteller-Artikelnummer::
17211839-100G
Lokale Artikelnummer::
MOLE17211839-100G
Beschreibung:
Aminoacetaldehyddiethylacetal
VE:
1 * 100 g
 This is a MarketSource item. Additional charges may apply
Lieferant:
Spectrum Chemical
Beschreibung:
Acesulfame potassium is a sugar substitute that contains no calories and is a white crystalline powder.
Lieferant:
NICKEL ELECTRO
Beschreibung:
Ultrasonic bath accessories, Wire basket, stainless steel, Für: Baths, 22 l
Lieferant:
Sigma-Aldrich
Beschreibung:
4,4'-(Hexafluorisopropyliden)diphthalsäureanhydrid, Sigma-Aldrich®
Artikel-Nr:
(MOLEM80404953)
Lieferant:
Molekula
Hersteller-Artikelnummer::
M80404953
Lokale Artikelnummer::
MOLEM80404953
Beschreibung:
1,3-Propansulton
VE:
1 * 25 g
This is a MarketSource item. Additional charges may apply
Lieferant:
MP Biomedicals
Beschreibung:
Synonym: D-threo-2,2-dichloro-N-[β-hydroxy-α-(hydroxymethyl)-p-(methyl- sulfonyl)phenethyl]-acetamide
Lieferant:
FLUOROCHEM
Beschreibung:
2-Benzyloxyphenylacetonitril
Artikel-Nr:
(PRSI90-519)
Lieferant:
ProSci Inc.
Hersteller-Artikelnummer::
90-519
Lokale Artikelnummer::
PRSI90-519
Beschreibung:
Interleukin-22 (IL-22), also known as IL-10 related T cell derived inducible factor (ILTIF) was initially identified as a gene induced by IL-9 in mouse T cells and mast cells. IL-22 has been shown to activate STAT1 and STAT3 in several hepatoma cell lines and upregulate the production of acute phase proteins. IL-22 is produced by normal T cells upon anti-CD3 stimulation in humans. Mouse IL-22 expression is also induced in various organs upon lipopolysaccharide injection, suggesting that IL-22 may be involved in inflammatory responses. The functional IL-22 receptor complex consists of two receptor subunits, IL-22R(CRF29) and IL-10Rbeta(CRF24), belonging to the class II cytokine receptor family.
VE:
1 * 25 µG
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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