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2-(2,4-Dichlorphenoxy)anilin+Hydrochlorid
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2-(2,4-Dichlorphenoxy)anilin+Hydrochlorid
Artikel-Nr:
(APOSOR930513-100G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR930513-100G
Lokale Artikelnummer::
APOSOR930513-100G
Beschreibung:
1-Phenyl-2-pyrrolidinon 98%
VE:
1 * 100 g
Artikel-Nr:
(APOSOR01684-100G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR01684-100G
Lokale Artikelnummer::
APOSOR01684-100G
Beschreibung:
4'-Bromacetophenon
VE:
1 * 100 g
Artikel-Nr:
(BOSSBS-11705R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11705R-HRP
Lokale Artikelnummer::
BOSSBS-11705R-HRP
Beschreibung:
AIP1 (ASK-interacting protein 1), also known as DAB2IP (DAB2 interacting protein), is a 1,189 amino acid protein that localizes to both the membrane and the cytoplasm and contains one Ras-GAP domain, one PH domain and one C2 domain. Expressed at low levels in prostate tissue, AIP1 functions as a Ras GTPase-activating protein that interacts with ASK 1 and, via this interaction, disrupts the association of ASK 1 with an inhibitory 14-3-3 complex, thereby allowing free ASK 1 to function within the cell. AIP1 exists as multiple alternatively spliced isoforms and is down-regulated in prostate cancer tissue, suggesting a role in tumor suppression. Chromosomal aberrations in the gene encoding AIP1 are associated with acute myeloid leukemia (AML), implicating a role for AIP1 fusion proteins in tumorigenesis.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11622R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11622R-CY7
Lokale Artikelnummer::
BOSSBS-11622R-CY7
Beschreibung:
Polycystin-1L3 is a 1,732 amino acid multi-pass membrane protein that contains one PLAT domain, one GPS domain and one C-type lectin domain. Expressed at high levels in placenta and present at lower levels in lung and heart, Polycystin-1L3 is thought to function as an ion-channel regulator that may interact with Polycystin-L and play a role in heteromeric taste channels. The gene encoding Polycystin-1L3 maps to human chromosome 16, which encodes over 900 genes and comprises nearly 3% of the human genome. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, as is Crohn's disease, which is a gastrointestinal inflammatory condition.
VE:
1 * 100 µl
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
MAPK/ERK Signalling Pathway
Artikel-Nr:
(BOSSBS-2617R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-2617R-A750
Lokale Artikelnummer::
BOSSBS-2617R-A750
Beschreibung:
Plays a role in the export of proteins that lack a signal peptide and are secreted by an alternative pathway. Binds two calcium ions per subunit. Binds one copper ion. Binding of one copper ion does not interfere with calcium binding. Required for the copper-dependent stress-induced export of IL1A and FGF1. The calcium-free protein binds to lipid vesicles containing phosphatidylserine, but not to vesicles containing phosphatidylcholine (By similarity).
VE:
1 * 100 µl
Lieferant:
Brady
Beschreibung:
Self-laminating polyester or vinyl labels for use with the BBP33 printer.
Lieferant:
Merck
Beschreibung:
3,3-Dimethylbutanon zur Synthese, Sigma-Aldrich®
Artikel-Nr:
(BOSSBS-9161R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9161R-A488
Lokale Artikelnummer::
BOSSBS-9161R-A488
Beschreibung:
The tripartite motif (TRIM) family of proteins are characterized by a conserved TRIM domain that includes a coiled-coil region, a B-box type zinc finger, one RING finger and three zinc-binding domains. TRIM17 (tripartite motif-containing 17), also known as RBCC, terf or RNF16, is a 477 amino acid protein that contains one RING-type zinc finger, one SPRY domain and one B box-type zinc finger. Expressed nearly exclusively in testis, TRIM17 belongs to the TRIM family and, based on its functional domains, may play a role in transcriptional regulation events. The gene encoding TRIM17 maps to human chromosome 1, which spans 260 million base pairs, contains over 3,000 genes and comprises nearly 8% of the human genome. Chromosome 1 houses a large number of disease-associated genes, including those that are involved in familial adenomatous polyposis, Stickler syndrome, Parkinson’s disease, Gaucher disease, schizophrenia and Usher syndrome. Aberrations in chromosome 1 are found in a variety of cancers, including head and neck cancer, malignant melanoma and multiple myeloma.
VE:
1 * 100 µl
Lieferant:
Avantor
Beschreibung:
L(+)-Ascorbinsäure 99,0-100,5%, feines Pulver USP, FCC, J.T.Baker®
Lieferant:
FLUOROCHEM
Beschreibung:
5-Chlor-2-iodbenzotrifluorid
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
6-(4-Chlorophenyl)-3-morpholinone 95%
Lieferant:
Alfa Aesar
Beschreibung:
Ammeline 90%, tech.
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
Maltol
Lieferant:
FLUOROCHEM
Beschreibung:
3,5-Dichlor-4-fluorbenzotrifluorid
Artikel-Nr:
(BOSSBS-9380R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9380R-CY7
Lokale Artikelnummer::
BOSSBS-9380R-CY7
Beschreibung:
Midline-1 (Tripartite motif-containing protein 18, Putative transcription factor XPRF, RING finger protein 59) is a 667 amino acid protein encoded by the human gene MID1. Midline-1 belongs to the TRIM/RBCC family and contains two B box-type zinc fingers, one B30.2/SPRY domain, one COS domain, one fibronectin type-III domain and one RING-type zinc finger. Midline-1 is believed to have E3 ubiquitin ligase activity which targets the catalytic subunit of protein phosphatase 2 for degradation. It is a cytoplasmic protein found as a homodimer or heterodimer with Midline-2. It also interacts with IGBP1 (Lymphocyte signaling protein A4). Defects in MID1 are the cause of Opitz syndrome type I (OS-I). OS-I is an X-linked recessive disorder characterized by hypertelorism, genital-urinary defects such as hypospadias in males and splayed labia in females, lip-palate-laryngotracheal clefts, imperforate anus, developmental delay and congenital heart defects. OS-I mutations produce proteins with a decreased affinity for microtubules.
VE:
1 * 100 µl
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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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