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1-Bromo-3-(2,2-difluoropropyl)benzene
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1-Bromo-3-(2,2-difluoropropyl)benzene
Artikel-Nr:
(APOSOR309232-5G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR309232-5G
Lokale Artikelnummer::
APOSOR309232-5G
Beschreibung:
8-Bromo-4-hydroxy-2-methylquinoline
VE:
1 * 5 g
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
4-Bromo-2-[bromo(difluoro)methyl]-1H-benzimidazole
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
2-Bromo-5-fluoro-4-hydroxypyridine
Lieferant:
Shenandoah Biotechnology
Beschreibung:
Interleukin 22 (IL-22), also called IL-TIF, is an IL-10 family member that is produced by activated dendritic cells and T lymphocytes. IL-22 signals via a heteroduplex receptor consisting of IL-22R and IL-10RB chains. IL-22 is a potent mediator of cellular inflammatory responses.
Artikel-Nr:
(EHERL20660000AL)
Lieferant:
EHRENSTORFER
Hersteller-Artikelnummer::
L20660000AL
Lokale Artikelnummer::
EHERL20660000AL
Beschreibung:
Organic Standard, 2,2'-Binaphthyl 10 µg/ml in Acetonitril, Packung: Glasflasche
VE:
1 * 10 mL
Artikel-Nr:
(PROOCILDLM28290.01)
Lieferant:
LGC Standards PROMOCHEM
Hersteller-Artikelnummer::
CILDLM28290.01
Lokale Artikelnummer::
PROOCILDLM28290.01
Beschreibung:
Dichlorvos-[Dimethyl-D6] (2,2-Dichlorvinyldimethylphosphat-[Dimethyl-D6], DDVP-[Dimethyl-D6]) (98% D)
VE:
1 * 10 mg
Artikel-Nr:
(APOSOR46136-5G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR46136-5G
Lokale Artikelnummer::
APOSOR46136-5G
Beschreibung:
5-Bromo-6-azaindole 98%
VE:
1 * 5 g
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
6-Bromo-2-hydrazino-3-methoxypyrazine
Artikel-Nr:
(BOSSBS-9174R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9174R-CY3
Lokale Artikelnummer::
BOSSBS-9174R-CY3
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-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15318R-A488
Lokale Artikelnummer::
BOSSBS-15318R-A488
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-15330R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15330R-A555
Lokale Artikelnummer::
BOSSBS-15330R-A555
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-15330R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15330R-CY7
Lokale Artikelnummer::
BOSSBS-15330R-CY7
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-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15314R-CY5
Lokale Artikelnummer::
BOSSBS-15314R-CY5
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-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15314R-A750
Lokale Artikelnummer::
BOSSBS-15314R-A750
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-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15314R-A647
Lokale Artikelnummer::
BOSSBS-15314R-A647
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:
APOLLO SCIENTIFIC
Beschreibung:
5-Bromo-2-chloro-4-fluoroanisole
Preis auf Anfrage
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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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