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3,5-Bis(trifluoromethyl)-\\u03B1-methylbenzylamine
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3,5-Bis(trifluoromethyl)-\\u03B1-methylbenzylamine
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
4-(Trifluoromethyl)-1-indanone
Artikel-Nr:
(BLDPBD108756-10G)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD108756-10G
Lokale Artikelnummer::
BLDPBD108756-10G
Beschreibung:
6-Chlor-2-hydroxypyridin 98%
VE:
1 * 10 g
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
Ethyl-4-(2-chloro-6-fluorophenyl)-2-methyl-6-oxo-1,4,5,6-tetrahydro-3-pyridinecarboxylate 97%
Artikel-Nr:
(BLDPBD2012-10G)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD2012-10G
Lokale Artikelnummer::
BLDPBD2012-10G
Beschreibung:
7-(4-Brombutoxy)-3,4-dihydro-2(1H)-chinolinon 97%
VE:
1 * 10 g
Artikel-Nr:
(BOSSBS-9616R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9616R
Lokale Artikelnummer::
BOSSBS-9616R
Beschreibung:
Ubr7 is a 425 amino acid protein that contains one UBR-type zinc finger and one PHD zinc finger. Participating in protein modification events within the N-end rule pathway, Ubr7 functions as an E3 ubiquitin-protein ligase that recognizes and binds proteins that contain destabilizing N-terminal residues, thereby leading to their ubiquitination and subsequent degradation.
VE:
1 * 100 µl
Lieferant:
Brady
Beschreibung:
Non-adhesive tag stock used for marking onthespot warning of dangerous conditions.
Artikel-Nr:
(BOSSBS-13084R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13084R-CY5
Lokale Artikelnummer::
BOSSBS-13084R-CY5
Beschreibung:
EPHEXIN is a 710 amino acid protein that localizes to both the membrane and the cytoplasm and contains one SH3 domain, one PH domain and one DH domain. Expressed at high levels in brain and present at lower levels in lung tissue, EPHEXIN interacts with EphA4 and functions as a guanine nucleotide exchange factor (GEF) that is capable of activating Rho A, Rac 1 and Cdc42 and is thought to play a role in axon guidance and growth cone collapse. EPHEXIN is subject to Src-dependent phosphorylation, an event that increases the GEF activity of EPHEXIN toward Rho A. Human EPHEXIN, which exists as multiple alternatively spliced isoforms, shares a high degree of sequence homology with its mouse counterpart, suggesting a conserved role between species.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11458R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11458R-CY3
Lokale Artikelnummer::
BOSSBS-11458R-CY3
Beschreibung:
EPHEXIN is a 710 amino acid protein that localizes to both the membrane and the cytoplasm and contains one SH3 domain, one PH domain and one DH domain. Expressed at high levels in brain and present at lower levels in lung tissue, EPHEXIN interacts with EphA4 and functions as a guanine nucleotide exchange factor (GEF) that is capable of activating Rho A, Rac 1 and Cdc42 and is thought to play a role in axon guidance and growth cone collapse. EPHEXIN is subject to Src-dependent phosphorylation, an event that increases the GEF activity of EPHEXIN toward Rho A. Human EPHEXIN, which exists as multiple alternatively spliced isoforms, shares a high degree of sequence homology with its mouse counterpart, suggesting a conserved role between species.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11489R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11489R-CY5
Lokale Artikelnummer::
BOSSBS-11489R-CY5
Beschreibung:
TNRC6B is a 1,723 amino acid protein that exists as two alternatively spliced isoforms and is thought to be involved in mRNA cleavage events. Expressed ubiquitously, TNRC6B contains one glycine/tryptophan (GW)-rich N-terminal domain, one central glutamine-rich region and one C-terminal RNA recognition motif and is encoded by a gene that maps to human chromosome 22. Mutations in several of the genes that map to chromosome 22 are involved in the development of Phelan-McDermid syndrome, Neurofibromatosis type 2, autism and schizophrenia. Additionally, translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia Chromosome and the subsequent production of the novel fusion protein BCR-Abl, a potent cell proliferation activator found in several types of leukemias.
VE:
1 * 100 µl
Lieferant:
ENTEGRIS
Beschreibung:
Conical pocket holds one wafer face down contacting only the edge of the wafer.
Artikel-Nr:
(BOSSBS-4820R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-4820R-HRP
Lokale Artikelnummer::
BOSSBS-4820R-HRP
Beschreibung:
Protein tyrosine-protein phosphatase required for T-cell activation through the antigen receptor. Acts as a positive regulator of T-cell coactivation upon binding to DPP4. The first PTPase domain has enzymatic activity, while the second one seems to affect the substrate specificity of the first one. Upon T-cell activation, recruits and dephosphorylates SKAP1 and FYN. Dephosphorylates LYN, and thereby modulates LYN activity (By similarity).
VE:
1 * 100 µl
Artikel-Nr:
(APOSPC6302-1G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
PC6302-1G
Lokale Artikelnummer::
APOSPC6302-1G
Beschreibung:
2-(Trifluoromethyl)xanthone
VE:
1 * 1 g
Lieferant:
Alfa Aesar
Beschreibung:
Thymolphthalein ACS
Artikel-Nr:
(BOSSBS-11622R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11622R
Lokale Artikelnummer::
BOSSBS-11622R
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
Artikel-Nr:
(BOSSBS-11622R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11622R-CY5
Lokale Artikelnummer::
BOSSBS-11622R-CY5
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
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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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