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3,4-(Ethylendioxy)benzylamin
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3,4-(Ethylendioxy)benzylamin
Artikel-Nr:
(BOSSBS-15323R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15323R-FITC
Lokale Artikelnummer::
BOSSBS-15323R-FITC
Beschreibung:
C9orf23 (chromosome 9 open reading frame 23) is a 163 amino acid protein that belongs to the histone-like Alba family and is encoded by a gene that maps to human chromosome 9p13.3. 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-15322R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15322R-A350
Lokale Artikelnummer::
BOSSBS-15322R-A350
Beschreibung:
C9orf21 (chromosome 9 open reading frame 21) is a 226 amino acid protein that belongs to the UPF0308 family and is encoded by a gene that maps to human chromosome 9q22.33. 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-15347R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15347R-CY7
Lokale Artikelnummer::
BOSSBS-15347R-CY7
Beschreibung:
Chromosome 9 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. The C9orf91 gene product has been provisionally designated C9orf91 pending further characterisation. There are three isoforms of C9orf91 that are produced as a result of alternative splicing events.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-15313R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15313R-A680
Lokale Artikelnummer::
BOSSBS-15313R-A680
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-15338R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15338R-A750
Lokale Artikelnummer::
BOSSBS-15338R-A750
Beschreibung:
Chromosome 9 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. The C9orf68 gene product has been provisionally designated C9orf68 pending further characterisation. There are two isoforms of C9orf68 that are produced as a result of alternative splicing events.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-15345R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15345R-A750
Lokale Artikelnummer::
BOSSBS-15345R-A750
Beschreibung:
Chromosome 9 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. The C9orf85 gene product has been provisionally designated C9orf85 pending further characterisation. There are three isoforms of C9orf85 that are produced as a result of alternative splicing events.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-15315R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15315R-CY5
Lokale Artikelnummer::
BOSSBS-15315R-CY5
Beschreibung:
C9orf142 (chromosome 9 open reading frame 142) is a 204 amino acid protein that exists as two alternatively spliced isoforms. The gene encoding C9orf142 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:
Flaschenhalsadapter, mit Gewinde, PP, Außen-Ø 22 mm, Calibrex™
Artikel-Nr:
(APOSOR361570-1G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR361570-1G
Lokale Artikelnummer::
APOSOR361570-1G
Beschreibung:
2,7-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrene
VE:
1 * 1 g
Artikel-Nr:
(BLEG408305)
Lieferant:
BIOLEGEND INC
Hersteller-Artikelnummer::
408305
Lokale Artikelnummer::
BLEG408305
Beschreibung:
Anti-FITC Mouse Monoclonal Antibody [clone: FIT-22]
VE:
1 * 100 µG
 This is a MarketSource item. Additional charges may apply
Lieferant:
MICRONOVA
Beschreibung:
Rechteckiger, 22 L Eimer mit einer inneren Breite von 482,6 mm, die ideale Lösung für ein Vielzahl an in kontrollierten Umgebungen verwendete Flach- und String-Mopps. Mit oder ohne 76,2 mm Schwerlastrollen.
Artikel-Nr:
(217-0807)
Lieferant:
DWK Life Sciences
Hersteller-Artikelnummer::
286129409
Lokale Artikelnummer::
SCOT286129409
Beschreibung:
DURAN®, borosilicate glass 3.3, clear.
VE:
1 * 1 ST
Artikel-Nr:
(BURK9602-0200)
Lieferant:
BURKLE
Hersteller-Artikelnummer::
9602-0200
Lokale Artikelnummer::
BURK9602-0200
Beschreibung:
Made of PP, translucent.
VE:
1 * 1 ST
Lieferant:
Thermo Scientific
Beschreibung:
Diethylether, extra trocken 99.5% stabilisiert, AcroSeal®
Artikel-Nr:
(EHERL20018700IO)
Lieferant:
EHRENSTORFER
Hersteller-Artikelnummer::
L20018700IO
Lokale Artikelnummer::
EHERL20018700IO
Beschreibung:
Organic Standard, 2,2',3,4',5,5',6-Heptachlorbiphenyl (PCB Nr. 187) 10 µg/ml in Isooctan, Packung: Glasflasche
VE:
1 * 10 mL
Lieferant:
Sigma-Aldrich
Beschreibung:
Extent of labeling is 48% ethoxyl.
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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