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1,2-Bis(4-chlorophenyl)ethylenediamine
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1,2-Bis(4-chlorophenyl)ethylenediamine
Artikel-Nr:
(USBIA2298-76P)
Lieferant:
US Biological
Hersteller-Artikelnummer::
A2298-76P
Lokale Artikelnummer::
USBIA2298-76P
Beschreibung:
Anti-ATG12 Mouse monoclonal antibody unconjugated [clone: 9G313]
VE:
1 * 100 µG
Lieferant:
Alfa Aesar
Beschreibung:
Ethyl-N-hydroxyacetimidat ≥97%
Artikel-Nr:
(BOSSBS-9289R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9289R-A488
Lokale Artikelnummer::
BOSSBS-9289R-A488
Beschreibung:
The deduced 257 amino acid protein PACRG (Parkin co-regulated gene) shows potential links to the ubiquitin/proteasome system. PACRG and Parkin are attached in a head-to-head arrangement on opposite DNA strands and share a common 5' flanking promoter region. The PACRG gene maps to chromosome 6q26; Northern blot analysis detects PACRG expression in all tissues examined except placenta. Using a positional cloning strategy in 197 Vietnamese leprosy simplex families (i.e. families with two unaffected parents and one affected child), significant connections between leprosy and 17 markers in the 5' regulatory region that PARK2 and PACRG share were observed. Possession of two or more of the 17 risk alleles is highly predictive of leprosy.PACRG is a gene located very close to parkin, in reverse orientation on the chromosome. It is thought to be co-transcribed with parkin by a bi-directional promoter between the two genes.
VE:
1 * 100 µl
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
Benzo[d]isothiazol-3-amine 95%
Artikel-Nr:
(H26096.03)
Lieferant:
Alfa Aesar
Hersteller-Artikelnummer::
H26096.03
Lokale Artikelnummer::
ALFAH26096.03
Beschreibung:
3,6-Difluorphthalsäure ≥98%
VE:
1 * 1 g
Lieferant:
BLD PHARMATECH GMBH
Beschreibung:
Motesanib diphosphate 98%
Artikel-Nr:
(APOSOR0120-25G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR0120-25G
Lokale Artikelnummer::
APOSOR0120-25G
Beschreibung:
3-Methoxythiophenol
VE:
1 * 25 g
Artikel-Nr:
(APOSPC510315-1G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
PC510315-1G
Lokale Artikelnummer::
APOSPC510315-1G
Beschreibung:
Ethyl 2,2-Difluoro-2-(2-nitrophenyl)acetate
VE:
1 * 1 g
Artikel-Nr:
(BLDPBD80475-100MG)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD80475-100MG
Lokale Artikelnummer::
BLDPBD80475-100MG
Beschreibung:
3-Benzyloxy-4-methylphenylamine 95%
VE:
1 * 100 mg
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
3-Bromo-4-hydroxyphenylsulphur pentafluoride
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
3-Bromo-2,5,6-trifluorobenzoic acid 98%
Artikel-Nr:
(APOSPC8036-1G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
PC8036-1G
Lokale Artikelnummer::
APOSPC8036-1G
Beschreibung:
1-(2-Bromo-5-fluorobenzoyl)pyrrolidine
VE:
1 * 1 g
Artikel-Nr:
(BOSSBS-11003R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11003R-CY5
Lokale Artikelnummer::
BOSSBS-11003R-CY5
Beschreibung:
Encoding over 1,100 genes within 132 million bases, chromosome 12 makes up about 4.5% of the human genome. A number of skeletal deformities are linked to chromosome 12 including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Noonan syndrome, which includes heart and facial developmental defects among the primary symptoms, is caused by a mutant form of PTPN11 gene product, SH-PTP2. Chromosome 12 is also home to a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction. Trisomy 12p leads to facial development defects, seizure disorders and a host of other symptoms varying in severity depending on the extent of mosaicism and is most severe in cases of complete trisomy. The FAM62A gene product has been provisionally designated FAM62A pending further characterization.
VE:
1 * 100 µl
Lieferant:
Thermo Scientific
Beschreibung:
4-Hydroxyphthalsäure 98%
Artikel-Nr:
(BOSSBS-6987R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-6987R-A350
Lokale Artikelnummer::
BOSSBS-6987R-A350
Beschreibung:
C12orf23 (chromosome 12 open reading frame 23), also known as FLJ11721, FLJ13959 or MGC17943, is a 116 amino acid multi-pass membrane protein belonging to the UPF0444 family. C12orf23 is encoded by a gene located on human chromosome 12, which encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a number of skeletal deformities, including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Noonan syndrome, which includes heart and facial developmental defects among the primary symptoms, is caused by a mutant form of PTPN11 gene product, SH-PTP2. Chromosome 12 is also home to a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction. Trisomy 12p leads to facial development defects, seizure disorders and a host of other symptoms varying in severity depending on the extent of mosaicism and is most severe in cases of complete trisomy.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-6987R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-6987R-CY7
Lokale Artikelnummer::
BOSSBS-6987R-CY7
Beschreibung:
C12orf23 (chromosome 12 open reading frame 23), also known as FLJ11721, FLJ13959 or MGC17943, is a 116 amino acid multi-pass membrane protein belonging to the UPF0444 family. C12orf23 is encoded by a gene located on human chromosome 12, which encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a number of skeletal deformities, including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Noonan syndrome, which includes heart and facial developmental defects among the primary symptoms, is caused by a mutant form of PTPN11 gene product, SH-PTP2. Chromosome 12 is also home to a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction. Trisomy 12p leads to facial development defects, seizure disorders and a host of other symptoms varying in severity depending on the extent of mosaicism and is most severe in cases of complete trisomy.
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.
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