(4-Chloro-3-pyridinyl)methanol
Artikel-Nr:
(BOSSBS-13472R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13472R-CY5
Lokale Artikelnummer::
BOSSBS-13472R-CY5
Beschreibung:
GTPases from the MMR1/HSR1 GTP-binding protein subfamily are circularly rearranged G-motifs that play a critical role in maintaining normal cell growth. Deletion of these genes results in severe growth defects with a marked reduction in mature rRNA species and a concomitant accumulation of the 35S pre-rRNA transcript. Deletion also causes the ribosomal protein Rpl25a to fail exportation from the nucleolus. Deletion of any of the G-domain motifs will result in a null phenotype and nuclear/nucleolar localization that lacks the nucleolar export of preribosomes and is accompanied by a distortion of the nucleolar structure. GNL3L (guanine nucleotide binding protein-like 3 (nucleolar)-like) is a 582 amino acid nuclear protein that belongs to the MMR1/HSR1 GTP-binding protein family. Containing one G (guanine nucleotide-binding) domain, GNL3L is required for normal processing of ribosomal pre-rRNA and for cell proliferation.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9084R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9084R-A647
Lokale Artikelnummer::
BOSSBS-9084R-A647
Beschreibung:
Belonging to the F-box family of proteins, FBXO35 (F-box only protein 35), also designated F-box and WD-40 domain-containing protein 12 (FBXW12 or FBXO12), is a 464 amino acid protein that contains one C-terminal F-box domain. F-box proteins are critical components of the SCF (Skp1-CUL-1-F-box protein)-type E3 ubiquitin ligase complex and are involved in substrate recognition and recruitment for ubiquitination. They are members of a larger family of proteins that are involved in the regulation of a wide variety of cellular mechanisms, including the cell cycle, the immune response, signaling cascades and developmental processes. They function by targeting proteins, such as cyclins, cyclin-dependent kinase inhibitors, I˚B-å and ∫-catenin, for degradation by the proteasome after ubiquitination. Via its F-box domain, FBXO35 can directly interact with Skp1 p19 and CUL-1. FBXO35 is ubiquitously expressed at low levels in most human tissues.
VE:
1 * 100 µl
Artikel-Nr:
(USBI042248)
Lieferant:
US Biological
Hersteller-Artikelnummer::
042248
Lokale Artikelnummer::
USBI042248
Beschreibung:
Anti-SPO11 Rabbit Polyclonal Antibody
VE:
1 * 200 µl
Lieferant:
Sigma-Aldrich
Beschreibung:
Homopiperazin, Sigma-Aldrich®
Artikel-Nr:
(MOLE28635108-100G)
Lieferant:
Molekula
Hersteller-Artikelnummer::
28635108-100G
Lokale Artikelnummer::
MOLE28635108-100G
Beschreibung:
PIPES Dinatriumsalz
VE:
1 * 100 g
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Artikel-Nr:
(MOLE12844702-25G)
Lieferant:
Molekula
Hersteller-Artikelnummer::
12844702-25G
Lokale Artikelnummer::
MOLE12844702-25G
Beschreibung:
D(-)-Asparaginsäure
VE:
1 * 25 g
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Artikel-Nr:
(MANA91680)
Lieferant:
MACHEREY-NAGEL
Hersteller-Artikelnummer::
91680
Lokale Artikelnummer::
MANA91680
Beschreibung:
Accessory for test kit, Reaktionsröhrchen mit 14 mm Innen-Ø
VE:
1 * 20 ST
Artikel-Nr:
(1076137.)
Lieferant:
USP
Hersteller-Artikelnummer::
1076137
Lokale Artikelnummer::
USPH1076137
Beschreibung:
USP Reference Standards are specified for use in conducting official USP–NF tests and assays. To confirm accuracy and reproducibility, USP Reference Standards are rigorously tested and evaluated by multiple independent laboratories including USP, commercial, regulatory, and academic labs. USP also provide publicly available, official documentary standards for pharmaceutical ingredients in the USP–NF that link directly with our primary reference standards.
VE:
1 * 15 mg
Artikel-Nr:
(BOSSBS-5474R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5474R-FITC
Lokale Artikelnummer::
BOSSBS-5474R-FITC
Beschreibung:
The classic group of MBP isoforms (isoform 4-isoform 14) are with PLP the most abundant protein components of the myelin membrane in the CNS. They have a role in both its formation and stabilization. The smaller isoforms might have an important role in remyelination of denuded axons in multiple sclerosis. The non-classic group of MBP isoforms (isoform 1-isoform 3/Golli-MBPs) may preferentially have a role in the early developing brain long before myelination, maybe as components of transcriptional complexes, and may also be involved in signaling pathways in T-cells and neural cells. Differential splicing events combined with optional post-translational modifications give a wide spectrum of isomers, with each of them potentially having a specialized function. Induces T-cell proliferation.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-2423R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-2423R-A647
Lokale Artikelnummer::
BOSSBS-2423R-A647
Beschreibung:
This gene encodes a transmembrane protein containing six epidermal growth factor repeats. The protein is involved in the differentiation of several cell types, including adipocytes; it is also thought to be a tumor suppressor. It is one of several imprinted genes located in a region of on chr 14q32. Certain mutations in this imprinted region can cause phenotypes similar to maternal and paternal uniparental disomy of chromosome 14 (UPD14). This gene is expressed from the paternal allele. A polymorphism within this gene has been associated with child and adolescent obesity. The mode of inheritance for this polymorphism is polar overdominance; this non-Mendelian inheritance pattern was first described in sheep with the callipyge phenotype, which is characterized by muscle hypertrophy and decreased fat mass. [provided by RefSeq, Mar 2010].
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13300R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13300R-A350
Lokale Artikelnummer::
BOSSBS-13300R-A350
Beschreibung:
GBE1 is a 702 amino acid protein that is expressed at high levels in muscle and liver and is involved in glycogen biosynthesis. Existing as a monomer, GBE1 catalyzes the transfer of alpha-1,4-linked glucosyl units from the outer end of a glycogen chain to an alpha-1,6 position on a neighboring glycogen chain and, via this catalytic activity, plays an essential role in glycogen accumulation. Defects in the gene encoding GBE1 are the cause of glycogen storage disease type 4 (GSD4) and adult polyglucosan body disease (APBD), the first of which is a metabolic disorder that is associated with the accumulation of polysaccharides and is characterized by liver disease during childhood. Unlike GSD4, APBD is a late-onset disorder that affects the central and peripheral nervous systems and is characterized by cognitive impairment, pyramidal tetraparesis and peripheral neuropathy.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-15165R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15165R-A488
Lokale Artikelnummer::
BOSSBS-15165R-A488
Beschreibung:
C3orf14 (chromosome 3 open reading frame 14), also known as HT021, is a 128 amino acid protein that is encoded by a gene mapping to human chromosome 3p14.2. Chromosome 3 is made up of approximately 214 million bases encoding over 1,100 genes. Notably, there is a chemokine receptor gene cluster and a variety of human cancer related loci on chromosome 3. Particular regions of the chromosome 3 short arm are deleted in many types of cancer cells. Key tumor suppressing genes on chromosome 3 encode apoptosis mediator RASSF1, cell migration regulator HYAL1 and angiogenesis suppressor SEMA3B. Marfan Syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth disease are a few of the numerous genetic diseases associated with chromosome 3.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-15165R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15165R-A647
Lokale Artikelnummer::
BOSSBS-15165R-A647
Beschreibung:
C3orf14 (chromosome 3 open reading frame 14), also known as HT021, is a 128 amino acid protein that is encoded by a gene mapping to human chromosome 3p14.2. Chromosome 3 is made up of approximately 214 million bases encoding over 1,100 genes. Notably, there is a chemokine receptor gene cluster and a variety of human cancer related loci on chromosome 3. Particular regions of the chromosome 3 short arm are deleted in many types of cancer cells. Key tumor suppressing genes on chromosome 3 encode apoptosis mediator RASSF1, cell migration regulator HYAL1 and angiogenesis suppressor SEMA3B. Marfan Syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth disease are a few of the numerous genetic diseases associated with chromosome 3.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13300R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13300R-HRP
Lokale Artikelnummer::
BOSSBS-13300R-HRP
Beschreibung:
GBE1 is a 702 amino acid protein that is expressed at high levels in muscle and liver and is involved in glycogen biosynthesis. Existing as a monomer, GBE1 catalyzes the transfer of alpha-1,4-linked glucosyl units from the outer end of a glycogen chain to an alpha-1,6 position on a neighboring glycogen chain and, via this catalytic activity, plays an essential role in glycogen accumulation. Defects in the gene encoding GBE1 are the cause of glycogen storage disease type 4 (GSD4) and adult polyglucosan body disease (APBD), the first of which is a metabolic disorder that is associated with the accumulation of polysaccharides and is characterized by liver disease during childhood. Unlike GSD4, APBD is a late-onset disorder that affects the central and peripheral nervous systems and is characterized by cognitive impairment, pyramidal tetraparesis and peripheral neuropathy.
VE:
1 * 100 µl
Artikel-Nr:
(FLUO011595-5G)
Lieferant:
FLUOROCHEM
Hersteller-Artikelnummer::
011595-5G
Lokale Artikelnummer::
FLUO011595-5G
Beschreibung:
(S)-(-)-Brombernsteinsäure
VE:
1 * 5 g
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Artikel-Nr:
(BOSSBS-3773R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-3773R-CY7
Lokale Artikelnummer::
BOSSBS-3773R-CY7
Beschreibung:
Modulation of the chromatin structure plays an important role in the regulation of transcription in eukaryotes. The nucleosome, made up of four core histone proteins (H2A, H2B, H3 and H4), is the primary building block of chromatin. The N-terminal tail of core histones undergoes different posttranslational modifications including acetylation, phosphorylation and methylation. These modifications occur in response to cell signal stimuli and have a direct effect on gene expression. In most species, the histone H2B is primarily acetylated at lysines 5, 12, 15 and 20. Histone H3 is primarily acetylated at lysines 9, 14, 18 and 23. Acetylation at lysine 9 appears to have a dominant role in histone deposition and chromatin assembly in some organisms. Phosphorylation at Ser10 of histone H3 is tightly correlated with chromosome condensation during both mitosis and meiosis.
VE:
1 * 100 µl
Preis auf Anfrage
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