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2,2\'-Difluorodiphenyldisulphide
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2,2\'-Difluorodiphenyldisulphide
Artikel-Nr:
(BOSSBS-13202R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13202R-CY5
Lokale Artikelnummer::
BOSSBS-13202R-CY5
Beschreibung:
Xenopus winged-helix factor, xFAST-1 (forkhead activin signal transducer-1) is a transcription factor that forms a complex with the receptor-regulated Smad protein, Smad2, and directly binds to activin response elements on DNA (1,2). The human homolog FAST-1 and the corresponding mouse homolog, designated FAST-2, share significant sequence homology with xFAST-1, including a conserved N-terminal forkhead domain that consists of 110 amino acid residues and is essential for binding DNA and regulating transcription in embryogenesis, in tumorigenesis and in the maintenance of differentiated cell states (3,4). FAST-1 and FAST-2 also contain a distinct C-terminal Smad interaction domain that is required for the association with various Smad proteins, including Smad2, Smad3 and Smad4 (3,5). Expression of FAST-1 and FAST-2 is predominantly observed during early development, with lower levels detected in adult tissues (6,7). FAST-1 and FAST-2 mediated DNA binding is attenuated by both TFGß and activin, indicating that these FAST proteins mediate TFGß induced signal transduction (3).
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9394R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9394R-A750
Lokale Artikelnummer::
BOSSBS-9394R-A750
Beschreibung:
WD-repeats are motifs that are found in a variety of proteins and are characterised by a conserved core of 40-60 amino acids that commonly form a tertiary propeller structure. While proteins that contain WD-repeats participate in a wide range of cellular functions, they are generally involved in regulatory mechanisms concerning chromatin assembly, cell cycle control, signal transduction, RNA processing, apoptosis and vesicular trafficking. WDR40A (WD-repeat-containing protein 40A), also known as DDB1- CUL4-associated factor 12, is a 453 amino acid cytoplasmic protein that contains four WD-repeats. WDR40A is highly expressed in some cancer cell lines, lung cancer tissues and normal testis. A probable substrate receptor for CUL4-DDB1 E3 ubiquitin-protein ligase complex, WRD40A is suggested to interact with DDB1. WDR40A is encoded by a gene mapping to human chromosome 9p13.3. Human chromosome 9 houses over 900 genes and comprises nearly 4% of the human genome.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-15154R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15154R-A680
Lokale Artikelnummer::
BOSSBS-15154R-A680
Beschreibung:
C12orf56 (chromosome 12 open reading frame 56), also known as PRO1853 or protein midA homolog, is a 441 amino acid mitochondrial protein that belongs to the midA family. Existing as two alternatively spliced isoforms, C12orf56 is encoded by a gene that maps to human chromosome 2p22.2. As the second largest human chromosome, chromosome 2 makes up approximately 8% of the human genome and contains 237 million bases encoding over 1,400 genes. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstr syndrome, is related to mutations in the ALMS1 gene. Chromosome 2 contains a probable vestigial second centromere as well as vestigial telomeres, which gives credence to the hypothesis that human chromosome 2 formed as a result of an ancient fusion of two ancestral chromosomes, which are still present in modern day apes.
VE:
1 * 100 µl
Artikel-Nr:
(PROONE5612)
Lieferant:
LGC Standards PROMOCHEM
Hersteller-Artikelnummer::
NE5612
Lokale Artikelnummer::
PROONE5612
Beschreibung:
Organic Standard, 1,2-Dichlorethan 5.000 µg/ml in Methanol, Packung: Glasflasche
VE:
1 * 1,5 mL
Artikel-Nr:
(EHERXA12370000ME)
Lieferant:
EHRENSTORFER
Hersteller-Artikelnummer::
XA12370000ME
Lokale Artikelnummer::
EHERXA12370000ME
Beschreibung:
Organic Standard, 1,2-Dichlorbenzol 100 µg/ml in Methanol, Packung: Glasflasche
VE:
1 * 1 mL
Artikel-Nr:
(EHERXA12422200ME)
Lieferant:
EHRENSTORFER
Hersteller-Artikelnummer::
XA12422200ME
Lokale Artikelnummer::
EHERXA12422200ME
Beschreibung:
Organic Standard, 1,2-Dichlorethan 100 µg/ml in Methanol, Packung: Glasflasche
VE:
1 * 1 mL
Artikel-Nr:
(BSBTPA2103)
Lieferant:
BosterBio
Hersteller-Artikelnummer::
PA2103
Lokale Artikelnummer::
BSBTPA2103
Beschreibung:
Rabbit IgG polyclonal antibody for Inactive caspase-12(CASP12) detection. Tested with WB, IHC-P in Human.
VE:
1 * 0,1 mg
Artikel-Nr:
(HUBE3968)
Lieferant:
HUBER
Hersteller-Artikelnummer::
3968
Lokale Artikelnummer::
HUBE3968
Beschreibung:
Tubings, insulated, Gummi, Tubing int.Ø: 17 mm, Wandstärke: 12 mm
VE:
1 * 1 m
Artikel-Nr:
(BOSSBS-11956R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11956R
Lokale Artikelnummer::
BOSSBS-11956R
Beschreibung:
The leucine-rich (LRR) repeat is a 20-30 amino acid motif that forms a hydrophobic å/∫ horseshoe fold, allowing it to accommodate several leucine residues within a tightly packed core. All LRR repeats contain a variable segment and a highly conserved segment, the latter of which accounts for 11 or 12 residues of the entire LRR motif. SLITRK3 (SLIT and NTRK-like family, member 3) is a 977 amino acid single-pass type I membrane protein that contains 20 LRR repeats and belongs to the SLITRK family. Expressed at highest levels in cerebral cortex, SLITRK3 is also found in adult and fetal neural tissues and some astrocytic brain tumors. SLITRK3 functions to suppress neurite outgrowth and plays a role in the regulation of neuronal function. SLITRK3 is encoded by a gene that maps to human chromosome 3, which houses over 1,100 genes, including a chemokine receptor (CKR) gene cluster and a variety of human cancer-related gene loci.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11956R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11956R-A647
Lokale Artikelnummer::
BOSSBS-11956R-A647
Beschreibung:
The leucine-rich (LRR) repeat is a 20-30 amino acid motif that forms a hydrophobic å/∫ horseshoe fold, allowing it to accommodate several leucine residues within a tightly packed core. All LRR repeats contain a variable segment and a highly conserved segment, the latter of which accounts for 11 or 12 residues of the entire LRR motif. SLITRK3 (SLIT and NTRK-like family, member 3) is a 977 amino acid single-pass type I membrane protein that contains 20 LRR repeats and belongs to the SLITRK family. Expressed at highest levels in cerebral cortex, SLITRK3 is also found in adult and fetal neural tissues and some astrocytic brain tumors. SLITRK3 functions to suppress neurite outgrowth and plays a role in the regulation of neuronal function. SLITRK3 is encoded by a gene that maps to human chromosome 3, which houses over 1,100 genes, including a chemokine receptor (CKR) gene cluster and a variety of human cancer-related gene loci.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-5827R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5827R-HRP
Lokale Artikelnummer::
BOSSBS-5827R-HRP
Beschreibung:
PCDHGB5 is a member of the protocadherin gamma gene cluster, one of three related clusters tandemly linked on chromosome five. These gene clusters have an immunoglobulin-like organization, suggesting that a novel mechanism may be involved in their regulation and expression. The gamma gene cluster includes 22 genes divided into 3 subfamilies. Subfamily A contains 12 genes, subfamily B contains 7 genes and 2 pseudogenes, and the more distantly related subfamily C contains 3 genes. The tandem array of 22 large, variable region exons are followed by a constant region, containing 3 exons shared by all genes in the cluster. Each variable region exon encodes the extracellular region, which includes 6 cadherin ectodomains and a transmembrane region. The constant region exons encode the common cytoplasmic region. These neural cadherin-like cell adhesion proteins most likely play a critical role in the establishment and function of specific cell-cell connections in the brain. Alternative splicing has been described for the gamma cluster genes.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11512R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11512R-CY3
Lokale Artikelnummer::
BOSSBS-11512R-CY3
Beschreibung:
Bardet-Biedl syndrome (BBS) is a pleiotropic genetic disorder characterized by obesity, photoreceptor degeneration, polydactyly, hypogenitalism, renal abnormalities, and developmental delay. Other associated clinical findings in BBS patients include diabetes, hypertension, and congenital heart defects. BBS genes map to multiple loci and encode fourteen proteins, BBS1-BBS14. Many BBS genes encode basal body or cilia proteins, suggesting that BBS is a ciliary dysfunction disorder. BBS10 (Bardet-Biedl syndrome 10), also known as chromosome 12 open reading fame 58, C12orf58 or FLJ23560, is a novel 723 amino acid protein belonging to the TCP-1 chaperonin family. BBS10 localizes to the basal body of primary cilium and assists in protein folding upon ATP hydrolysis. Inhibition of BBS10 has been found to impair ciliogenesis, activate the glycogen synthase kinase 3 pathway and cause peroxisome proliferator-activated receptor nuclear accumulation. The gene encoding BBS10 contains two exons and maps to human chromosome 12q21.2.
VE:
1 * 100 µl
Lieferant:
PERKIN ELMER GC INSTRUMENTS
Beschreibung:
Rack, Chromatography vial, Bohrung Ø: 50 mm, Bohrungen: 12 (2×6)
Artikel-Nr:
(USBI146142)
Lieferant:
US Biological
Hersteller-Artikelnummer::
146142
Lokale Artikelnummer::
USBI146142
Beschreibung:
Anti-FAF1 Rabbit Polyclonal Antibody
VE:
1 * 100 µG
Lieferant:
ACROBIOSYSTEMS
Beschreibung:
Human recombinant IL-12 R beta 1 (from HEK293 cells)
Lieferant:
GERBER FUNKE
Beschreibung:
Borosilikatglas.
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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