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1-Bromo-3-(2,2-difluoropropyl)benzene


61 940  results were found

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Lieferant:  Alfa Aesar
Beschreibung:   6-Bromo-2,4-dimethylpyridine-3-boronic acid 95%
Artikel-Nr: (BOSSBS-15313R-FITC)

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-15313R-FITC
Lokale Artikelnummer:: BOSSBS-15313R-FITC
Beschreibung:   C9orf139 (chromosome 9 open reading frame 139) is a 190 amino acid 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-15317R-CY5)

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-15317R-CY5
Lokale Artikelnummer:: BOSSBS-15317R-CY5
Beschreibung:   C9orf163 (chromosome 9 open reading frame 163) is a 203 amino acid 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-15313R-CY7)

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-15313R-CY7
Lokale Artikelnummer:: BOSSBS-15313R-CY7
Beschreibung:   C9orf139 (chromosome 9 open reading frame 139) is a 190 amino acid 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-15343R-FITC)

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-15343R-FITC
Lokale Artikelnummer:: BOSSBS-15343R-FITC
Beschreibung:   C9orf79 is a 1445 amino acid single-pass membrane protein that belongs to the FAM75 family. The gene encoding C9orf79 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
Artikel-Nr: (BOSSBS-15343R-CY3)

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-15343R-CY3
Lokale Artikelnummer:: BOSSBS-15343R-CY3
Beschreibung:   C9orf79 is a 1445 amino acid single-pass membrane protein that belongs to the FAM75 family. The gene encoding C9orf79 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:  APOLLO SCIENTIFIC
Beschreibung:   5-Bromo-1H-pyrazol-3-amine 97%
Lieferant:  APOLLO SCIENTIFIC
Beschreibung:   4-Bromo-1H-imidazo[4,5-c]pyridine

Lieferant:  BLD PHARMATECH GMBH
Hersteller-Artikelnummer:: BD161137-10G
Lokale Artikelnummer:: BLDPBD161137-10G
Beschreibung:   Ethyl-5-bromo-1,3,4-thiadiazole-2-carboxylate 97%
VE:  1 * 10 g
Lieferant:  APOLLO SCIENTIFIC
Beschreibung:   2-Bromo-4-(1,1-difluoroethyl)-1-fluorobenzene 97%
Lieferant:  APOLLO SCIENTIFIC
Beschreibung:   6-Bromo-3-chloro-2,4-difluoroaniline 97%
Artikel-Nr: (BOSSBS-6264R-CY3)

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-6264R-CY3
Lokale Artikelnummer:: BOSSBS-6264R-CY3
Beschreibung:   EMP-2 is a 167 amino acid multi-pass membrane protein that contains four-transmembrane domains and belongs to the GAS3/PMP22 (growth arrest-specific-3/peripheral myelin protein-22) family. Localized to lipid raft domains in the plasma membrane, EMP-2 regulates the expression of several target proteins and is necessary for blastocyst implantation in the uterine endometrium. Specifically, EMP-2 mediates blastocyst implantation by controlling the cell membrane expression of MHC and glycosylphosphatidylinositol-anchored proteins, as well as Integrins and caveolin-1. In adult tissues, EMP-2 is expressed in heart, lung, ovary and intestine, while fetal expression is highest in kidney, brain and liver. Overexpression of EMP-2 is associated with endometrial adenocarcinoma, suggesting a possible role for EMP-2 in tumorigenesis.
VE:  1 * 100 µl
Artikel-Nr: (APOSOR305400-250MG)

Lieferant:  APOLLO SCIENTIFIC
Hersteller-Artikelnummer:: OR305400-250MG
Lokale Artikelnummer:: APOSOR305400-250MG
Beschreibung:   6-Bromo-1H-pyrazolo[3,4-b]pyridine
VE:  1 * 250 mg
Artikel-Nr: (APOSOR305335-250MG)

Lieferant:  APOLLO SCIENTIFIC
Hersteller-Artikelnummer:: OR305335-250MG
Lokale Artikelnummer:: APOSOR305335-250MG
Beschreibung:   6-Bromo-1H-pyrazolo[4,3-c]pyridine
VE:  1 * 250 mg

Lieferant:  BLD PHARMATECH GMBH
Hersteller-Artikelnummer:: BD01191945-5G
Lokale Artikelnummer:: BLDPBD01191945-5G
Beschreibung:   3-(Triethoxysilyl)propyl 2-Bromo-2-methylpropanoate 95%
VE:  1 * 5 g
Lieferant:  APOLLO SCIENTIFIC
Beschreibung:   3-Bromo-7-methylimidazo[1,2-a]pyrimidine 97%
Preis auf Anfrage
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 call 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 call 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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