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3-Brom-2-fluor-5-methylphenylborons\\u00E4ure
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3-Brom-2-fluor-5-methylphenylborons\\u00E4ure
Artikel-Nr:
(BOSSBS-2604R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-2604R-A350
Lokale Artikelnummer::
BOSSBS-2604R-A350
Beschreibung:
Receptor for interleukin-12. This subunit is the signaling component coupling to the JAK2/STAT4 pathway. Promotes the proliferation of T-cells as well as NK cells. Induces the promotion of T-cells towards the Th1 phenotype by strongly enhancing IFN-gamma production.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-2604R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-2604R-A488
Lokale Artikelnummer::
BOSSBS-2604R-A488
Beschreibung:
Receptor for interleukin-12. This subunit is the signaling component coupling to the JAK2/STAT4 pathway. Promotes the proliferation of T-cells as well as NK cells. Induces the promotion of T-cells towards the Th1 phenotype by strongly enhancing IFN-gamma production.
VE:
1 * 100 µl
Lieferant:
Alfa Aesar
Beschreibung:
di-Silberoxid elektrische Qualität
Artikel-Nr:
(BOSSBS-11822R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11822R-A350
Lokale Artikelnummer::
BOSSBS-11822R-A350
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:
Thermo Scientific
Beschreibung:
N-(3-Brompropyl)phthalimid 98%
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
Artikel-Nr:
(BOSSBS-8130R-CY5.5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8130R-CY5.5
Lokale Artikelnummer::
BOSSBS-8130R-CY5.5
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. CCDC38 (coiled-coil domain containing 38) is a 563 amino acid protein encoded by a gene that maps to human chromosome 12q23.1. Encoding over 1,100 genes, chromosome 12 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-8130R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8130R-FITC
Lokale Artikelnummer::
BOSSBS-8130R-FITC
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. CCDC38 (coiled-coil domain containing 38) is a 563 amino acid protein encoded by a gene that maps to human chromosome 12q23.1. Encoding over 1,100 genes, chromosome 12 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:
(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
Lieferant:
ANSELL HEALTH CARE
Beschreibung:
Diese nahtlosen Nylonträger mit ¾- oder kompletter Nitril-Beschichtung bieten eine hohe Flexibilität und Fingerbeweglichkeit für einen maximalen Bedienkomfort.
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
5-(Pyridin-2-yl)thiophene-2-carbaldehyde
Artikel-Nr:
(BOSSBS-12345R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12345R-CY3
Lokale Artikelnummer::
BOSSBS-12345R-CY3
Beschreibung:
HEM1 is a 1,127 amino acid single-pass membrane protein that localizes to the cytoplasmic side of the cell membrane. One of several members of the highly conserved HEM family of tissue-specific transmembrane proteins, HEM1 is expressed in cells of hematopoietic origin where it is thought to play an important role in oogenesis. The gene encoding HEM1 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-12345R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12345R-CY5
Lokale Artikelnummer::
BOSSBS-12345R-CY5
Beschreibung:
HEM1 is a 1,127 amino acid single-pass membrane protein that localizes to the cytoplasmic side of the cell membrane. One of several members of the highly conserved HEM family of tissue-specific transmembrane proteins, HEM1 is expressed in cells of hematopoietic origin where it is thought to play an important role in oogenesis. The gene encoding HEM1 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:
(B21242.22)
Lieferant:
Alfa Aesar
Hersteller-Artikelnummer::
B21242.22
Lokale Artikelnummer::
ALFAB21242.22
Beschreibung:
2-Octinsäuremethylester ≥98%
VE:
1 * 100 g
Lieferant:
Biotium
Beschreibung:
This antibody recognizes an oncofetal glycoprotein with a single chain of 70 kDa, which is identified as alpha fetoprotein (AFP). This MAb is highly specific to AFP and shows no cross-reaction with other oncofetal antigens or serum albumin. AFP is normally synthesized in the liver, intestinal tract, and yolk sac of the fetus. Antibody to AFP has been shown to be useful in detecting hepatocellular carcinomas (HCC) and germ cell neoplasms, especially yolk sac tumors.
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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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