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1,1-Diphenylhydrazin+Hydrochlorid
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
AM095 free acid is a potent LPA1 receptor antagonist with IC50 values of 0.98 and 0.73 μM for recombinant human or mouse LPA1 respectively.
Lieferant:
Biotium
Beschreibung:
Reacts with a protein of 57 kDa, identified as the L1 protein of human papilloma virus type 16 (HPV-16). It is the major capsid protein of HPV-16. Infection with specific types of HPV has been associated with an increased risk of developing cervical neoplasia. HPV types 6 and 11 have been associated with relatively benign diseases such as genital warts but types 16 and 18 are strongly associated with cervical, vaginal, and vulvar malignancies. The antibody reacts very strongly with formalin-fixed, paraffin-embedded tissues containing HPV-16 or -33; very weak reactions were occasionally observed with biopsy specimens or smears containing HPV-6 or HPV-11. It cross-reacts with HPV37.
Artikel-Nr:
(BOSSBS-15143R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15143R-HRP
Lokale Artikelnummer::
BOSSBS-15143R-HRP
Beschreibung:
C2CD3 (C2 domain-containing protein 3), also known as FLJ34770, is a 2,353 amino acid protein that contains two C2 domains. C2 domains are regions of about 130 amino acid residues that are found in proteins that bind phospholipids. It is thought that calcium binding to the C2 domain induces an electrostatic potential change that enhances phospholipid binding, which suggests a role for the domain as an electrostatic switch. C2CD3 is expressed as five isoforms produced by alternative splicing events. The gene that encodes C2CD3 maps to human chromosome 11, which makes up around 4% of human genomic DNA. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and _ thalassemia are caused by HBB gene mutations. Wilms' tumors, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11.
VE:
1 * 100 µl
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
Methyl-3-cyclopropyl-1H-pyrazole-5-carboxylate
Artikel-Nr:
(APOSPC4893-250MG)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
PC4893-250MG
Lokale Artikelnummer::
APOSPC4893-250MG
Beschreibung:
Ethyl-2-{3-[(4-fluoroanilino)carbonyl]-2-pyridinyl}acetate
VE:
1 * 250 mg
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
5-Bromo-3-methylbenzo[b]thiophene-2-sulphonyl chloride
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
Boc-N-ME-PHG-OH 97%
Artikel-Nr:
(BOSSBS-13271R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13271R-CY3
Lokale Artikelnummer::
BOSSBS-13271R-CY3
Beschreibung:
The UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase (GalNAc-T) family of enzymes are substrate-specific proteins that catalyze the transfer of GalNAc (N-acetylgalactosamine) to serine and threonine residues onto various proteins, thereby initiating mucin-type O-linked glycosylation in the Golgi apparatus. GalNAc-T11 (Polypeptide N-acetylgalactosaminyltransferase 11), also known as UDP-GalNAc:polypeptide N-acetylgalactosaminyltransferase 11, is a 608 amino acid protein that catalyzes glycosylation of Muc1, Muc4.1 and EA2, though it does not display enzymatic preference for erythropoitein. The N-terminal domain is involved in substrate binding and manganese coordination, while the C-terminal domain is involved in UDP-Gal binding and catalytic reaction. GalNAc-T11 is highly expressed in kidney tubules, though it is not expressed in glomeruli. There are two isoforms of GalNAc-T11 that are produced as a result of alternative splicing events.
VE:
1 * 100 µl
Lieferant:
Cayman Chemical
Beschreibung:
Sisomicin is a broad-spectrum aminoglycoside antibiotic originally isolated from M. inyoensis.
Lieferant:
Alfa Aesar
Beschreibung:
2-Fluor-4-(trifluormethyl)phenylboronsäure ≥97%
Artikel-Nr:
(BOSSBS-8139R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8139R-A647
Lokale Artikelnummer::
BOSSBS-8139R-A647
Beschreibung:
The coiled-coil domain is a structural motif found in proteins that are involved in a diverse array of biological functions such as the regulation of gene expression, cell division, membrane fusion, and drug extrusion and delivery. CCDC83 (coiled-coil domain-containing protein 83), also known as HSD9, is 413 amino acid protein that exists as three alternatively spliced isoforms. The gene encoding CCDC83 maps to human chromosome 11, which houses over 1,400 genes and comprises nearly 4% of the human genome. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are associated with defects in genes that maps to chromosome 11.
VE:
1 * 100 µl
Artikel-Nr:
(ANSE38-628/11)
Lieferant:
ANSELL HEALTH CARE
Hersteller-Artikelnummer::
38-628/11
Lokale Artikelnummer::
ANSE38-628/11
Beschreibung:
Kombination aus Butyl- und Vitonschicht von 0,7 mm für maximalen Schutz vor gefährlichen Chemikalien.
VE:
1 * 1 PAAR
Artikel-Nr:
(BLDPBD216837-250MG)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD216837-250MG
Lokale Artikelnummer::
BLDPBD216837-250MG
Beschreibung:
Methyl-4-oxotetrahydro-2H-pyran-3-carboxylate 95%
VE:
1 * 250 mg
Artikel-Nr:
(BLDPBD145669-100MG)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD145669-100MG
Lokale Artikelnummer::
BLDPBD145669-100MG
Beschreibung:
N-[2-(Cyclohexyloxy)-4-nitrophenyl]methanesulphonamide 98%
VE:
1 * 100 mg
Artikel-Nr:
(BOSSBS-11631R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11631R-HRP
Lokale Artikelnummer::
BOSSBS-11631R-HRP
Beschreibung:
Olfactory receptors interact with odorant molecules in the nose to initiate a neuronal response that leads to the perception of smell. While they share a seven transmembrane domain structure with many neurotransmitter and hormone receptors, olfactory receptors are responsible for the recognition and transduction of odorant signals. OR10A2 (olfactory receptor 10A2) and OR10A5 (olfactory receptor 10A5) are multi-pass membrane proteins that belong to the G-protein coupled receptor 1 family and are encoded by genes that map to human chromosome 11p15.4. Chromosome 11 houses over 1,400 genes and comprises nearly 4% of the human genome. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are associated with defects in genes that map to chromosome 11.
VE:
1 * 100 µl
Lieferant:
Biotium
Beschreibung:
Reacts with a protein of 57 kDa, identified as the L1 protein of human papilloma virus type 16 (HPV-16). It is the major capsid protein of HPV-16. Infection with specific types of HPV has been associated with an increased risk of developing cervical neoplasia. HPV types 6 and 11 have been associated with relatively benign diseases such as genital warts but types 16 and 18 are strongly associated with cervical, vaginal, and vulvar malignancies. The antibody reacts very strongly with formalin-fixed, paraffin-embedded tissues containing HPV-16 or -33; very weak reactions were occasionally observed with biopsy specimens or smears containing HPV-6 or HPV-11. It cross-reacts with HPV37.
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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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