4-Fluorobenzo[d]thiazol-2(3H)-one
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
MAPK/ERK Signalling Pathway
Lieferant:
Alfa Aesar
Beschreibung:
Ammeline 90%, tech.
Lieferant:
Brady
Beschreibung:
Self-laminating polyester or vinyl labels for use with the BBP33 printer.
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
Maltol
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:
APOLLO SCIENTIFIC
Beschreibung:
6-(4-Chlorophenyl)-3-morpholinone 95%
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
Lieferant:
Alfa Aesar
Beschreibung:
Aluminiumoxid Substrat 10x10x1 mm, einseitig poliert C plane
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
1-(3-Chlor-5-(trifluormethyl)-2-pyridinyl)tetrahydro-4(1H)-pyridinon
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
5-(Morpholinomethyl)-2-thioxo-2,3-dihydro-4(1H)-pyrimidinone
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
5-(Bromoacetyl)-2,3-dihydro-1,4-benzodioxine
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
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
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