5-Cyan-1-isopropylbenzimidazol
Artikel-Nr:
(BOSSBS-15323R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15323R-A750
Lokale Artikelnummer::
BOSSBS-15323R-A750
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:
(BLDPBD01397511-50M)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD01397511-50M
Lokale Artikelnummer::
BLDPBD01397511-50M
Beschreibung:
(OC-6-21)-Tris[3,5-difluoro-2-(2-pyridinyl-κN)phenyl-κC]iridium 97%
VE:
1 * 50 mg
Artikel-Nr:
(SIALM89625-100G)
Lieferant:
Sigma-Aldrich
Hersteller-Artikelnummer::
M89625-100G
Lokale Artikelnummer::
SIALM89625-100G
Beschreibung:
Mucobromsäure, Sigma-Aldrich®
VE:
1 * 100 g
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
3-Amino-6,7-difluor-1H-indazol 95+%
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
1-Brom-2,5-difluor-4-nitrobenzol
Artikel-Nr:
(BOSSBS-15323R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15323R-CY5
Lokale Artikelnummer::
BOSSBS-15323R-CY5
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-15323R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15323R-CY7
Lokale Artikelnummer::
BOSSBS-15323R-CY7
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:
(BLDPBD82264-1G)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD82264-1G
Lokale Artikelnummer::
BLDPBD82264-1G
Beschreibung:
((2R,3R,5R)-3-(Benzoyloxy)-4,4-difluoro-5-((methylsulphonyl)oxy)tetrahydrofuran-2-yl)methyl benzoate 97%
VE:
1 * 1 g
Lieferant:
Restek
Beschreibung:
Organic Standard, 2,3-dichloropropionic acid, 1000 µg/ml, methyl <i>tert</i>-butyl ether, 1 ml/ampoule
Artikel-Nr:
(A18670.06)
Lieferant:
Alfa Aesar
Hersteller-Artikelnummer::
A18670.06
Lokale Artikelnummer::
ALFAA18670.06
Beschreibung:
1-Brom-2,5-difluor-4-nitrobenzol ≥97%
VE:
1 * 5 g
Artikel-Nr:
(MOLE35750747-100G)
Lieferant:
Molekula
Hersteller-Artikelnummer::
35750747-100G
Lokale Artikelnummer::
MOLE35750747-100G
Beschreibung:
Tiglinsäure
VE:
1 * 100 g
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Artikel-Nr:
(8.41368.0005)
Lieferant:
Merck
Hersteller-Artikelnummer::
8.41368.0005
Lokale Artikelnummer::
MERC8.41368.0005
Beschreibung:
Bis(4-fluorphenyl)sulfon, Sigma-Aldrich®
VE:
1 * 5 g
Lieferant:
Sigma-Aldrich
Beschreibung:
(+)-Dibenzoyl-D-weinsäure, Sigma-Aldrich®
Artikel-Nr:
(BOSSBS-9238R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9238R
Lokale Artikelnummer::
BOSSBS-9238R
Beschreibung:
The RING-type zinc finger motif is present in a number of viral and eukaryotic proteins and is made of a conserved cysteine-rich domain that is able to bind two zinc atoms. Proteins that contain this conserved domain are generally involved in the ubiquitination pathway of protein degradation. RNF23 (RING finger protein 23), also known as tripartite motif-containing protein 39 (TRIM39) or testis-abundant finger protein, is a 518 amino acid protein belonging to the TRIM/RBCC family that is known to interact with MOAP1. Ubiquitously expressed and existing as two alternatively spliced isoforms, RNF23 is found at highest levels in spleen, testis, brain, kidney, liver, heart and skeletal muscle. RNF23 typically localizes to cytosol but shifts to mitochondria upon co-localization with MOAP1, a short-lived, pro-apoptotic protein which RNF23 prevents from becoming poly-ubiquitinated and degraded, thereby facilitating apoptosis. RNF23 contains one B box-type zinc finger, a B30.2/SPRY domain and a single RING-type zinc finger.
VE:
1 * 100 µl
Artikel-Nr:
(BLDPBD01434565-1G)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD01434565-1G
Lokale Artikelnummer::
BLDPBD01434565-1G
Beschreibung:
Iridium-(4,4'-dimethoxy-2,2'-bipyridine-κN1,κN1')bis[3,5-difluoro-2-(5-fluoro-2-pyridinyl-κN)phenyl-κC]-hexafluorophosphate 97%
VE:
1 * 1 g
Artikel-Nr:
(BOSSBS-11805R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11805R-A750
Lokale Artikelnummer::
BOSSBS-11805R-A750
Beschreibung:
AT-motif binding factor 1 (ATBF1) binds to the AT-rich core sequence element in the human a-fetoprotein enhancer. Alternative splicing generates the ATBF1-A and ATBF1-B. While ATBF1-A contains a 920-amino acid extension at the N-terminus, both ATBF1-A and ATBF1-B contain 4 DNA-binding homeobox domains. Additionally, ATBF1-A contains 23 zinc finger motifs while ATBF1-B contains 18 zinc finger motifs. The N-terminal extension unique to ATBF1-A has transcriptional repressor activity. In the small intestine, ATBF1-A inhibits expression of the brushborder enzyme aminopeptidase-N through direct binding to the AT motif element. Besides functioning in transcription regulation, ATBF1 also functions in ATPase activity. ATPase activity associated with ATBF1-A is DNA/RNA-dependent and requires both homeobox domains and zinc finger motifs. ATBF1 is highly expressed in spleen and brain tissues. The gene encoding human ATBF1 maps to chromosome 16q22.3-q23.1.
VE:
1 * 100 µl
Preis auf Anfrage
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