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2,3-Difluoro-4-methoxycinnamic+acid
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2,3-Difluoro-4-methoxycinnamic+acid
Artikel-Nr:
(BOSSBS-0241R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-0241R-A555
Lokale Artikelnummer::
BOSSBS-0241R-A555
Beschreibung:
The attachment of enveloped viruses to cells and the fusion of viral and cellular membranes are critical early events in the HIV viral infection. This process is mediated by envelope glycoproteins (gp) on the surface of the virus. The human immunodeficiency virus type 1 (HIV-1) envelope glycoprotein, gp160, is proteolytically cleaved into gp120 and gp41, which remain noncovalently associated with one another. gp120 is one of the proteins that forms the envelope of HIV. gp120 projects from the surface of HIV and binds to the CD4 molecule on helper T cells. gp120 has been a logical experimental HIV vaccine because the outer envelope is the first part of the virus that encounters antibody. gp41 is embedded in the outer envelope of HIV that anchors gp120. gp41 also plays a key role in HIV's infection of CD4+ T cells by facilitating the fusion of the viral and cell membranes. The nomenclature of the gp proteins describes their respective molecular masses (e.g., gp160, gp120, gp41).
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9295R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9295R-HRP
Lokale Artikelnummer::
BOSSBS-9295R-HRP
Beschreibung:
ANKRD17 is a 2,603 amino acid protein that contains 25 ankyrin repeats and one KH domain. ANKRD17 is expressed in bone marrow and is thought to be involved in liver development. ANKRD17 localizes to the cytoplasm and the nucleus. ANKRD17 exists as five alternatively spliced isoforms that are encoded by a gene which maps to human chromosome 4. Representing approximately 6% of the human genome, chromosome 4 contains nearly 900 genes. Notably, the Huntingtin gene, which is found to encode an expanded glutamine tract in cases of Huntington's disease, is on chromosome 4. FGFR-3 is also encoded on chromosome 4 and has been associated with thanatophoric dwarfism, achondroplasia, Muenke syndrome and bladder cancer. Chromosome 4 is also tied to Ellis-van Creveld syndrome, methylmalonic acidemia and polycystic kidney disease. Chromosome 4 reportedly contains the largest gene deserts (regions of the genome with no protein encoding genes) and has one of the two lowest recombination frequencies of the human chromosomes.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9295R-CY5.5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9295R-CY5.5
Lokale Artikelnummer::
BOSSBS-9295R-CY5.5
Beschreibung:
ANKRD17 is a 2,603 amino acid protein that contains 25 ankyrin repeats and one KH domain. ANKRD17 is expressed in bone marrow and is thought to be involved in liver development. ANKRD17 localizes to the cytoplasm and the nucleus. ANKRD17 exists as five alternatively spliced isoforms that are encoded by a gene which maps to human chromosome 4. Representing approximately 6% of the human genome, chromosome 4 contains nearly 900 genes. Notably, the Huntingtin gene, which is found to encode an expanded glutamine tract in cases of Huntington's disease, is on chromosome 4. FGFR-3 is also encoded on chromosome 4 and has been associated with thanatophoric dwarfism, achondroplasia, Muenke syndrome and bladder cancer. Chromosome 4 is also tied to Ellis-van Creveld syndrome, methylmalonic acidemia and polycystic kidney disease. Chromosome 4 reportedly contains the largest gene deserts (regions of the genome with no protein encoding genes) and has one of the two lowest recombination frequencies of the human chromosomes.
VE:
1 * 100 µl
Artikel-Nr:
(BLDPBD01123462-100)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD01123462-100
Lokale Artikelnummer::
BLDPBD01123462-100
Beschreibung:
Ethyl 4-chloro-5-(trifluoromethyl)quinoline-3-carboxylate 98%
VE:
1 * 100 mg
Lieferant:
Thermo Scientific
Beschreibung:
N,N-Dimethylethylendiamin 99%
Artikel-Nr:
(115-2032)
Lieferant:
KIMBERLY CLARK
Hersteller-Artikelnummer::
7622
Lokale Artikelnummer::
KIMB7622
Beschreibung:
Feste, fusselarme, wiederverwendbare Wischtücher für die Reinigung mit Chemikalien und Lösungsmitteln. Hervorragend geeignet zum Reinigen von Oberflächen (auch Glasoberflächen) in Druckereien, Produktionsbereichen und Kfz-Werkstätten.
VE:
1 * 420 ST
Artikel-Nr:
(BOSSBS-11034R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11034R-A488
Lokale Artikelnummer::
BOSSBS-11034R-A488
Beschreibung:
MYBPC1 is a 1,141 amino acid protein that contains three fibronectin type-III domains and seven Ig-like C2-type domains. Existing as a member of the immunoglobulin superfamily, MYBPC1 functions as a thick filament-associated protein that localizes to striated muscle bands in vertebrae and is thought to modify the activity of select ATPases. Additionally, MYBPC1 may play a role in the modulation of muscle contraction and in the overall structural integrity of the cell. The gene encoding MYBPC1 maps to human chromosome 12, which encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and Trisomy 12p, which causes facial developmental defects and seizure disorders.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11034R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11034R-CY7
Lokale Artikelnummer::
BOSSBS-11034R-CY7
Beschreibung:
MYBPC1 is a 1,141 amino acid protein that contains three fibronectin type-III domains and seven Ig-like C2-type domains. Existing as a member of the immunoglobulin superfamily, MYBPC1 functions as a thick filament-associated protein that localizes to striated muscle bands in vertebrae and is thought to modify the activity of select ATPases. Additionally, MYBPC1 may play a role in the modulation of muscle contraction and in the overall structural integrity of the cell. The gene encoding MYBPC1 maps to human chromosome 12, which encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and Trisomy 12p, which causes facial developmental defects and seizure disorders.
VE:
1 * 100 µl
Lieferant:
ANSELL HEALTH CARE
Beschreibung:
Diese nahtlosen Nylonträger mit ¾- oder kompletter Nitril-Beschichtung bieten eine hohe Flexibilität und Fingerbeweglichkeit für einen maximalen Bedienkomfort.
Artikel-Nr:
(BOSSBS-11822R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11822R-CY3
Lokale Artikelnummer::
BOSSBS-11822R-CY3
Beschreibung:
CSAD is a 493 amino acid protein that exists as a homodimer and belongs to the group II decarboxylase family. CSAD catalyzes the conversion of 3-sulfino-L-alanine to hypotaurine and carbon dioxide, binds pyridoxal phosphate as a cofactor and undergoes alternative splicing to produce three isoforms. The gene encoding CSAD maps to human chromosome 12, which encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders.
VE:
1 * 100 µl
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
FITC (Fluorescein-5-isothiocyanat, Fluoresceinisothiocyanat Isomer I)
Lieferant:
Alfa Aesar
Beschreibung:
4,4'-Dibrombenzil ≥97%
Lieferant:
Alfa Aesar
Beschreibung:
3,4-Dicyananilin 98%
Lieferant:
VWR Chemicals
Beschreibung:
N,N-Dimethylformamid ≥99,8%, AnalaR NORMAPUR® ACS, Reag. Ph. Eur. analytisches Reagens
Artikel-Nr:
(9222-01)
Lieferant:
Avantor
Lokale Artikelnummer::
BAKR9222-01
Beschreibung:
N,N-Dimethylformamid ≥99,8% (durch GC, auf Wasserinhalt korrigiert), PHOTREX® für die Spektrophotometrie, J.T.Baker®
VE:
1 * 500 mL
Artikel-Nr:
(BOSSBS-11210R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11210R
Lokale Artikelnummer::
BOSSBS-11210R
Beschreibung:
Dyneins are multisubunit, high molecular weight ATPases that interact with microtubules to generate force by converting the chemical energy of ATP into the mechanical energy of movement. Cytoplasmic or axonemal Dynein heavy, intermediate, light and light-intermediate chains are all components of minus end-directed motors; the complex transports cellular cargos towards the central region of the cell. Axonemal dynein motors contain one to three non-identical heavy chains and cause a sliding of microtubules in the axonemes of cilia and flagella in a mechanism necessary for cilia to beat and propel the cell. DNAH9 (Dynein, axonemal, heavy chain 9), also known as DYH9, HL20, DNEL1, Dnahc9 or DNAH17L, is a member of the Dynein heavy chain family and comprises one of the heavy chain subunits of axonemal Dynein. DNAH9 consists of an N-terminal stem which is responsible for interacting with other Dynein components and binding cargo, and four P-loops that comprise the motor domain at its C-terminus.
VE:
1 * 100 µl
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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.
Dieses Produkt kann nur an eine Lieferadresse versandt werden die über die entsprechende Lizenzen verfügt. Für weitere Hilfe bitte kontaktieren Sie Ihr VWR Vertriebszentrum.
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