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Methyl+trans-3-hydroxycyclobutanecarboxylate
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Methyl+trans-3-hydroxycyclobutanecarboxylate
Lieferant:
GLW
Beschreibung:
PP, natur oder farbig, ohne Trennelemente.
Artikel-Nr:
(EHERC13330000)
Lieferant:
EHRENSTORFER
Hersteller-Artikelnummer::
C13330000
Lokale Artikelnummer::
EHERC13330000
Beschreibung:
2-Imidazolidinthion
VE:
1 * 0,25 g
Lieferant:
Sigma-Aldrich
Beschreibung:
N-Decyl-N,N-dimethyl-3-ammonio-1-propansulfonat (Sulfobetain-10, SB-10), Sigma-Aldrich®
Lieferant:
Corning Life Science
Beschreibung:
A complete range of classical cell culture media are available.
Artikel-Nr:
(221-0133)
Lieferant:
GLASWARENFABRIK KARL HECHT
Hersteller-Artikelnummer::
44000016
Lokale Artikelnummer::
HECH44000016
Beschreibung:
Borosilikatglas 3.3
VE:
1 * 1 ST
Lieferant:
TOURNAIRE-EMBALLAGE
Beschreibung:
Aus reinem Aluminium.
Artikel-Nr:
(229-0311)
Lieferant:
DWK Life Sciences
Hersteller-Artikelnummer::
286338101
Lokale Artikelnummer::
SCOT286338101
Beschreibung:
Polyester (PBT). Zur stufenlosen Regulierung der Durchflussmengen in Schlauchverbindungen.
VE:
1 * 1 ST
Lieferant:
SciLabware
Beschreibung:
Screw cap, made of PP, for media-lab bottles
Lieferant:
DWK Life Sciences
Beschreibung:
DURAN®, Borosilikatglas 3.3, klar.
Artikel-Nr:
(EPSC23-CTP4/PF)
Lieferant:
EP SCIENTIFIC
Hersteller-Artikelnummer::
23-CTP4/PF
Lokale Artikelnummer::
EPSC23-CTP4/PF
Beschreibung:
Klarglas, mit Urea-Verschluss
VE:
1 * 72 ST
Artikel-Nr:
(BOSSBS-11698R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11698R-A350
Lokale Artikelnummer::
BOSSBS-11698R-A350
Beschreibung:
Huntingtin yeast partner E is a 458 amino acid single-pass membrane protein. HYPE is thought to interact with Huntingtin, a protein which induces neurodegeneration when mutated. HYPE also contains two tetratricopeptide repeats (TPR), which may be involved in protein-protein interaction. The gene that encodes HYPE is located on chromosome 12, which encodes over 1,100 genes within 132 million bases and makes up about 4.5% of the human genome. A number of skeletal deformities are linked to chromosome 12 including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Chromosome 12 is also home to a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction. Trisomy 12p leads to facial development defects, seizure disorders and a host of other symptoms varying in severity depending on the extent of mosaicism and is most severe in cases of complete trisomy.
VE:
1 * 100 µl
Artikel-Nr:
(BNUM0513-50)
Lieferant:
Biotium
Hersteller-Artikelnummer::
BNUM0513-50
Lokale Artikelnummer::
BTIUBNUM0513-50
Beschreibung:
Recognizes a 53 kDa protein, which is identified as p53 suppressor gene product. It reacts with the mutant as well as the wild form of p53. Its epitope maps within the N-terminus (aa 37-45) of p53. Monoclonal antibody PAb1801 does not block the binding of DO-7 MAb to p53 in an ELISA test. p53 is a tumor suppressor gene expressed in a wide variety of tissue types and is involved in regulating cell growth, replication, and apoptosis. It binds to MDM2, SV40 T antigen and human papilloma virus E6 protein. Positive nuclear staining with p53 antibody has been reported to be a negative prognostic factor in breast carcinoma, lung carcinoma, colorectal, and urothelial carcinoma. Anti-p53 positivity has also been used to differentiate uterine serous carcinoma from endometrioid carcinoma as well as to detect intratubular germ cell neoplasia. Mutations involving p53 are found in a wide variety of malignant tumors, including breast, ovarian, bladder, colon, lung, and melanoma.
VE:
1 * 50 µl
Artikel-Nr:
(BOSSBS-6987R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-6987R-A750
Lokale Artikelnummer::
BOSSBS-6987R-A750
Beschreibung:
C12orf23 (chromosome 12 open reading frame 23), also known as FLJ11721, FLJ13959 or MGC17943, is a 116 amino acid multi-pass membrane protein belonging to the UPF0444 family. C12orf23 is encoded by a gene located on human chromosome 12, which encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a number of skeletal deformities, including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Noonan syndrome, which includes heart and facial developmental defects among the primary symptoms, is caused by a mutant form of PTPN11 gene product, SH-PTP2. Chromosome 12 is also home to a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction. Trisomy 12p leads to facial development defects, seizure disorders and a host of other symptoms varying in severity depending on the extent of mosaicism and is most severe in cases of complete trisomy.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-6987R-CY5.5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-6987R-CY5.5
Lokale Artikelnummer::
BOSSBS-6987R-CY5.5
Beschreibung:
C12orf23 (chromosome 12 open reading frame 23), also known as FLJ11721, FLJ13959 or MGC17943, is a 116 amino acid multi-pass membrane protein belonging to the UPF0444 family. C12orf23 is encoded by a gene located on human chromosome 12, which encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a number of skeletal deformities, including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Noonan syndrome, which includes heart and facial developmental defects among the primary symptoms, is caused by a mutant form of PTPN11 gene product, SH-PTP2. Chromosome 12 is also home to a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction. Trisomy 12p leads to facial development defects, seizure disorders and a host of other symptoms varying in severity depending on the extent of mosaicism and is most severe in cases of complete trisomy.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13247R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13247R-A750
Lokale Artikelnummer::
BOSSBS-13247R-A750
Beschreibung:
Heterotrimeric G proteins function to relay information from cell surface receptors to intracellular effectors. Each of a very broad range of receptors specifically detects an extracellular stimulus (a photon, pheromone, odorant, hormone or neurotransmitter) while the effectors (i.e., adenyl cyclase), which act to generate one or more intracellular messengers, are less numerous. In mammals, G protein Alpha, Beta and Gamma polypeptides are encoded by at least 16, 4 and 7 genes, respectively. Most interest in G proteins has been focused on their Alpha subunits, since these proteins bind and hydrolyze GTP and most obviously regulate the activity of the best studied effectors. Four distinct classes of G Alpha subunits have been identified; these include G Alpha s, G Alpha i, G Alpha q and G Alpha 12/13. The two members of the fourth class of G Alpha subunit proteins, G Alpha 12 and G Alpha 13, are insensitive to ADP-ribosylation by pertussis toxin, share 67% identity with each other and less than 45% identity with other G Alpha subunits and are widely expressed in a broad range of tissues.
VE:
1 * 100 µl
Artikel-Nr:
(SEMA1102)
Lieferant:
SEMADENI
Hersteller-Artikelnummer::
1102
Lokale Artikelnummer::
SEMA1102
Beschreibung:
LDPE, translucent.
VE:
1 * 1 ST
Preis auf Anfrage
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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.
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