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1-[2-Oxo-2-(2-pyridyl)ethyl]pyridinium+iodide
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1-[2-Oxo-2-(2-pyridyl)ethyl]pyridinium+iodide
Artikel-Nr:
(BOSSBS-11034R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11034R-A350
Lokale Artikelnummer::
BOSSBS-11034R-A350
Beschreibung:
MYBPC1 is a 1,141 amino acid protein that contains three fibronectin type-III domains and seven Ig-like C2-type domains. Existing as a member of the immunoglobulin superfamily, MYBPC1 functions as a thick filament-associated protein that localizes to striated muscle bands in vertebrae and is thought to modify the activity of select ATPases. Additionally, MYBPC1 may play a role in the modulation of muscle contraction and in the overall structural integrity of the cell. The gene encoding MYBPC1 maps to human chromosome 12, which encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and Trisomy 12p, which causes facial developmental defects and seizure disorders.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11034R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11034R-A750
Lokale Artikelnummer::
BOSSBS-11034R-A750
Beschreibung:
MYBPC1 is a 1141 amino acid protein that contains three fibronectin type-III domains and seven Ig-like C2-type domains. Existing as a member of the immunoglobulin superfamily, MYBPC1 functions as a thick filament-associated protein that localizes to striated muscle bands in vertebrae and is thought to modify the activity of select ATPases. Additionally, MYBPC1 may play a role in the modulation of muscle contraction and in the overall structural integrity of the cell. The gene encoding MYBPC1 maps to human chromosome 12, which encodes over 1100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and Trisomy 12p, which causes facial developmental defects and seizure disorders.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11034R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11034R-CY3
Lokale Artikelnummer::
BOSSBS-11034R-CY3
Beschreibung:
MYBPC1 is a 1,141 amino acid protein that contains three fibronectin type-III domains and seven Ig-like C2-type domains. Existing as a member of the immunoglobulin superfamily, MYBPC1 functions as a thick filament-associated protein that localizes to striated muscle bands in vertebrae and is thought to modify the activity of select ATPases. Additionally, MYBPC1 may play a role in the modulation of muscle contraction and in the overall structural integrity of the cell. The gene encoding MYBPC1 maps to human chromosome 12, which encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and Trisomy 12p, which causes facial developmental defects and seizure disorders.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9958R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9958R-A750
Lokale Artikelnummer::
BOSSBS-9958R-A750
Beschreibung:
CWF19L1 is a 538 amino acid protein belonging to the CWF19 family and exists as three alternatively spliced isoforms. CWF19L1 is encoded by a gene located on human chromosome 10, which spans nearly 135 million base pairs, makes up approximately 4.5% of total DNA in cells and encodes nearly 1,200 genes. Several protein-coding genes, including those that encode for chemokines, cadherins, excision repair proteins, early growth response factors (Egrs) and fibroblast growth receptors (FGFRs), are located on chromosome 10. Defects in some of the genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman's syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8302R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8302R-A350
Lokale Artikelnummer::
BOSSBS-8302R-A350
Beschreibung:
GLT8D2 (glycosyltransferase 8 domain-containing protein 2), also known as GALA4A, is a 349 amino acid single-pass type II membrane protein. A member of the glycosyltransferase 8 family, GLT8D2 is encoded by a gene that maps to human chromosome 12q23.3. Encoding over 1,100 genes within 132 million base pairs, chromosome 12 makes up about 4.5% of the human genome. A number of skeletal deformities are linked to chromosome 12, including hypochondrogenesis, achondrogenesis, Noonan syndrome, Kniest dysplasia and trisomy 12p. Chromosome 12 is also home to a homeobox gene cluster, which encodes crucial transcription factors for morphogenesis, as well as the natural killer complex gene cluster, which encodes C-type lectin proteins that mediate the NK cell response to MHC I interaction.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8579R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8579R-CY3
Lokale Artikelnummer::
BOSSBS-8579R-CY3
Beschreibung:
The finding that mutations in DNA mismatch repair genes are associated with hereditary nonpolyposis colorectal cancer (HNPCC) has resulted in considerable interest in the understanding of the mechanism of DNA mismatch repair. Initially, inherited mutations in the MSH2 and MLH1 homologs of the bacterial DNA mismatch repair genes MutS and MutL were demonstrated at high frequency in HNPCC and were shown to be associated with microsatellite instability. The demonstration that 10 to 45% of pancreatic, gastric, breast, ovarian and small cell lung cancers also display microsatellite instability has been interpreted to suggest that DNA mismatch repair is not restricted to HNPCC tumors but is a common feature in tumor initiation or progression. Two additional homologs of the prokaryotic MutL gene, designated PMS1 and PMS2, have been identified and shown to be mutated in the germline of HNPCC patients.
VE:
1 * 100 µl
Lieferant:
Bernd Kraft
Beschreibung:
Bromthymolblau 0,1% in Ethanol
Lieferant:
SIGMA ALDRICH MICROSCOPY
Beschreibung:
bisBenzimide H 33258 has been used for nuclear staining in cells. bisBenzimide H 33258 is useful for staining DNA, chromosomes and nuclei. bisBenzimide H 33258 may be used for fluorescence microscopy or flow cytometry.
Artikel-Nr:
(91126.001)
Lieferant:
VWR Chemicals
Lokale Artikelnummer::
VWRC91126.001
Beschreibung:
A standard mixture, typically used for food testing, containing the following components: 100 ug/ml each of Abamectin [CAS:71751-41-2] ; Acetamiprid [CAS:135410-20-7] ; Ametryn [CAS:834-12-8] ; Amitraz [CAS:33089-61-1] ; Azoxystrobin [CAS:131860-33-8] ; Benalaxyl [CAS:71626-11-4] ; Benzoximate [CAS:29104-30-1] ; Boscalid [CAS:188425-85-6] ; Butafenacil [CAS:134605-64-4] ; Carbetamide [CAS:16118-49-3] ; Carfentrazone-ethyl [CAS:128639-02-1] ; Chlorantraniliprole [CAS:500008-45-7] ; Clofentezine [CAS:74115-24-5] ; Cymoxanil [CAS:57966-95-7] ; Cyprodinil [CAS:121552-61-2] ; Cyromazine [CAS:66215-27-8] ; Dimoxystrobin [CAS:149961-52-4] ; Dinotefuran [CAS:165252-70-0] ; Doramectin [CAS:117704-25-3] ; Eprinomectin [CAS:123997-26-2] ; Famoxadone [CAS:131807-57-3] ; Fenazaquin [CAS:120928-09-8] ; Fenhexamid [CAS:126833-17-8] ; Fenpyroximate [CAS:111812-58-9] ; Flonicamid [CAS:158062-67-0] ; Fluazinam [CAS:79622-59-6] ; Fludioxonil [CAS:131341-86-1] ; Fluoxastrobin [CAS:361377-29-9] ; Flutolanil [CAS:66332-96-5] ; Furalaxyl [CAS:57646-30-7] ; Halofenozide [CAS:112226-61-6] ; Imazalil [CAS:35554-44-0] ; Imidacloprid [CAS:138261-41-3] ; Ivermectine [CAS:70288-86-7] ; Kresoxim-methyl [CAS:143390-89-0] ; Mandipropamid [CAS:374726-62-2] ; Mepanipyrim [CAS:110235-47-7] ; Mepronil [CAS:55814-41-0] ; Metaflumizone [CAS:139968-49-3] ; Metalaxyl [CAS:57837-19-1] ; Methoxyfenozide [CAS:161050-58-4] ; Moxidectin [CAS:113507-06-5] ; Myclobutanil [CAS:88671-89-0] ; Nitenpyram [CAS:150824-47-8] ; Oxadixyl [CAS:77732-09-3] ; Picoxystrobin [CAS:117428-22-5] ; Piperonyl butoxide [CAS:51-03-6] ; Prochloraz [CAS:67747-09-5] ; Prometon [CAS:1610-18-0] ; Pymetrozine [CAS:123312-89-0] ; Pyracarbolid [CAS:24691-76-7] ; Pyrimethanil [CAS:53112-28-0] ; Pyriproxyfen [CAS:95737-68-1] ; Quinoxyfen [CAS:124495-18-7] ; Rotenone [CAS:83-79-4] ; Secbumeton [CAS:26259-45-0] ; Spiroxamine [CAS:118134-30-8] ; Tebufenozide [CAS:112410-23-8] ; Tebufenpyrad [CAS:119168-77-3] ; Terbumeton [CAS:33693-04-8] ; Triadimefon [CAS:43121-43-3] ; Trifloxystrobin [CAS:141517-21-7] ; Zoxamide [CAS:156052-68-5] in Acetonitrile
VE:
1 * 1 mL
Artikel-Nr:
(PROOCIL-PCB-67-C)
Lieferant:
LGC Standards PROMOCHEM
Hersteller-Artikelnummer::
CIL-PCB-67-C
Lokale Artikelnummer::
PROOCIL-PCB-67-C
Beschreibung:
2,3',4,5-Tetrachlorbiphenyl (PCB Nr. 67)
VE:
1 * 5 mg
Artikel-Nr:
(PROOCIL-PCB-48-C)
Lieferant:
LGC Standards PROMOCHEM
Hersteller-Artikelnummer::
CIL-PCB-48-C
Lokale Artikelnummer::
PROOCIL-PCB-48-C
Beschreibung:
2,2',4,5-Tetrachlorbiphenyl (PCB Nr. 48)
VE:
1 * 5 mg
Artikel-Nr:
(BOSSBS-4965R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-4965R-A350
Lokale Artikelnummer::
BOSSBS-4965R-A350
Beschreibung:
The finding that mutations in DNA mismatch repair genes are associated with hereditary nonpolyposis colorectal cancer (HNPCC) has resulted in considerable interest in the understanding of the mechanism of DNA mismatch repair. Initially, inherited mutations in the MSH2 and MLH1 homologs of the bacterial DNA mismatch repair genes MutS and MutL were demonstrated at high frequency in HNPCC and were shown to be associated with microsatellite instability. The demonstration that 10 to 45% of pancreatic, gastric, breast, ovarian and small cell lung cancers also display microsatellite instability has been interpreted to suggest that DNA mismatch repair is not restricted to HNPCC tumors but is a common feature in tumor initiation or progression. Two additional homologs of the prokaryotic MutL gene, designated PMS1 and PMS2, have been identified and shown to be mutated in the germline of HNPCC patients.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-7648R-CY5.5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-7648R-CY5.5
Lokale Artikelnummer::
BOSSBS-7648R-CY5.5
Beschreibung:
Apoptosis is a cell death process that removes toxic and/or useless cells during mammalian development. The apoptotic process is accompanied by shrinkage and fragmentation of the cells and nuclei and degradation of the chromosomal DNA into nucleosomal units. DNA fragmentation factor (DFF) is a heterodimeric protein of 40-kD (DFFB) and 45-kD (DFFA) subunits. DFFA is the substrate for caspase-3 and triggers DNA fragmentation during apoptosis. DFF becomes activated when DFFA is cleaved by caspase-3. The cleaved fragments of DFFA dissociate from DFFB, the active component of DFF. DFFB has been found to trigger both DNA fragmentation and chromatin condensation during apoptosis. Alternatively spliced transcript variants encoding distinct isoforms have been found for this gene but the biological validity of these variants has not been determined. [provided by RefSeq, Jul 2008].
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-7648R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-7648R-A555
Lokale Artikelnummer::
BOSSBS-7648R-A555
Beschreibung:
Apoptosis is a cell death process that removes toxic and/or useless cells during mammalian development. The apoptotic process is accompanied by shrinkage and fragmentation of the cells and nuclei and degradation of the chromosomal DNA into nucleosomal units. DNA fragmentation factor (DFF) is a heterodimeric protein of 40-kD (DFFB) and 45-kD (DFFA) subunits. DFFA is the substrate for caspase-3 and triggers DNA fragmentation during apoptosis. DFF becomes activated when DFFA is cleaved by caspase-3. The cleaved fragments of DFFA dissociate from DFFB, the active component of DFF. DFFB has been found to trigger both DNA fragmentation and chromatin condensation during apoptosis. Alternatively spliced transcript variants encoding distinct isoforms have been found for this gene but the biological validity of these variants has not been determined. [provided by RefSeq, Jul 2008].
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-4965R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-4965R-A488
Lokale Artikelnummer::
BOSSBS-4965R-A488
Beschreibung:
The finding that mutations in DNA mismatch repair genes are associated with hereditary nonpolyposis colorectal cancer (HNPCC) has resulted in considerable interest in the understanding of the mechanism of DNA mismatch repair. Initially, inherited mutations in the MSH2 and MLH1 homologs of the bacterial DNA mismatch repair genes MutS and MutL were demonstrated at high frequency in HNPCC and were shown to be associated with microsatellite instability. The demonstration that 10 to 45% of pancreatic, gastric, breast, ovarian and small cell lung cancers also display microsatellite instability has been interpreted to suggest that DNA mismatch repair is not restricted to HNPCC tumors but is a common feature in tumor initiation or progression. Two additional homologs of the prokaryotic MutL gene, designated PMS1 and PMS2, have been identified and shown to be mutated in the germline of HNPCC patients.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11861R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11861R-A350
Lokale Artikelnummer::
BOSSBS-11861R-A350
Beschreibung:
HAP1 (huntingtin-associated protein 1) binds to huntingtin (1). Huntingtin is a protein that contains a polyglutamine region and when the number of glutamine repeats exceeds 35, the gene encodes a version of huntingtin that leads to Huntington’s disease (HD) (2,3). The ability of HAP1 to bind to huntingtin is enhanced by an expanded polyglutamine repeat region (1). HAP1 shows neuronal localization and moves with huntingtin in nerve fibers (4,5). HAP1 is primarily expressed in brain tissue, with greater expression in the olfactory bulb and brain stem (1). Mouse HAP1 is localized to membrane-bound organelles including large endosomes, tubulovesicular structures and budding vesicles in neurons (6). Duo, also designated huntingtin-associated protein interacting protein or HAPIP, binds Huntingtin-associated protein 1 (HAP1) and may have a role in vesicle trafficking and cytoskeletal function.
VE:
1 * 100 µl
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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.
Dieses Produkt kann nur an eine Lieferadresse versandt werden die über die entsprechende Lizenzen verfügt. Für weitere Hilfe bitte kontaktieren Sie Ihr VWR Vertriebszentrum.
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