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(1-Ethyl-1H-imidazol-5-yl)methanol
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(1-Ethyl-1H-imidazol-5-yl)methanol
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
2-Acetyl-3-chloro-5-(trifluoromethyl)pyridine
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
2-(tert-Butoxy)-2-oxoethylzinc bromide 0.5M in Diethylether
Artikel-Nr:
(BOSSBS-9448R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9448R-HRP
Lokale Artikelnummer::
BOSSBS-9448R-HRP
Beschreibung:
The tetraspanin family is a group of cell surface proteins that regulate cell development, activation, growth and motility. Each member contains four hydrophobic domains and participates in the mediation of signal transduction. NET-5, also known as TSPAN9 (tetraspanin 9), is a 239 amino acid multi-pass membrane protein that belongs to the tetraspanin (TM4SF) family. NET-5 forms a complex with GPVI in the tetraspanin microdomains on the platelet surface, and is encoded by a gene that maps to human chromosome 12p13.33. Chromosome 12 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:
4-Aminobuttersäure 99+%
Artikel-Nr:
(BLDPBD286686-100MG)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD286686-100MG
Lokale Artikelnummer::
BLDPBD286686-100MG
Beschreibung:
3-Amino-5-fluor-1-methyl-1H-indazol 98%
VE:
1 * 100 mg
Lieferant:
Thermo Scientific
Beschreibung:
D-Glucoronic acid 98%
Artikel-Nr:
(BOSSBS-9448R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9448R-A750
Lokale Artikelnummer::
BOSSBS-9448R-A750
Beschreibung:
The tetraspanin family is a group of cell surface proteins that regulate cell development, activation, growth and motility. Each member contains four hydrophobic domains and participates in the mediation of signal transduction. NET-5, also known as TSPAN9 (tetraspanin 9), is a 239 amino acid multi-pass membrane protein that belongs to the tetraspanin (TM4SF) family. NET-5 forms a complex with GPVI in the tetraspanin microdomains on the platelet surface, and is encoded by a gene that maps to human chromosome 12p13.33. Chromosome 12 encodes over 1100 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-9448R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9448R-A488
Lokale Artikelnummer::
BOSSBS-9448R-A488
Beschreibung:
The tetraspanin family is a group of cell surface proteins that regulate cell development, activation, growth and motility. Each member contains four hydrophobic domains and participates in the mediation of signal transduction. NET-5, also known as TSPAN9 (tetraspanin 9), is a 239 amino acid multi-pass membrane protein that belongs to the tetraspanin (TM4SF) family. NET-5 forms a complex with GPVI in the tetraspanin microdomains on the platelet surface, and is encoded by a gene that maps to human chromosome 12p13.33. Chromosome 12 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-11451R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11451R-HRP
Lokale Artikelnummer::
BOSSBS-11451R-HRP
Beschreibung:
Advillin is an 819 amino acid protein that localizes to both the cytoplasm and the cytoskeleton and contains one HP domain and six gelsolin-like repeats. Expressed at high levels in colon and small intestine and at lower levels in uterus, thymus, testis and prostate, advillin functions as a calcium-regulated Actin-binding protein that may be involved in the development of neuronal cells, specifically those that form ganglia. The gene encoding advillin 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-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11034R-A350
Lokale Artikelnummer::
BOSSBS-11034R-A350
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-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11034R-A750
Lokale Artikelnummer::
BOSSBS-11034R-A750
Beschreibung:
MYBPC1 is a 1141 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 1100 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-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11034R-CY3
Lokale Artikelnummer::
BOSSBS-11034R-CY3
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:
(APOSOR61157-1G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR61157-1G
Lokale Artikelnummer::
APOSOR61157-1G
Beschreibung:
2-(4-Bromophenyl)-2-azaspiro[4.4]nonane-1,3-dione
VE:
1 * 1 g
Artikel-Nr:
(APOSOR33444-1G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR33444-1G
Lokale Artikelnummer::
APOSOR33444-1G
Beschreibung:
tert-Butyl-4-hydroxydihydro-2(3H)-isoxazolecarboxylate 95%
VE:
1 * 1 g
Artikel-Nr:
(BOSSBS-11398R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11398R-A680
Lokale Artikelnummer::
BOSSBS-11398R-A680
Beschreibung:
This gene is a member of the synaptotagmin gene family and encodes a protein similar to other family members that mediate calcium-dependent regulation of membrane trafficking in synaptic transmission. Studies of the orthologous gene in rat have shown that the encoded protein selectively modulates spontaneous synaptic-vesicle exocytosis and may also be involved in regulating calcium independent secretion in nonneuronal cells. Alternative splicing results in multiple transcript variants. The gene has previously been referred to as synaptotagmin XI but has been renamed synaptotagmin XII to be standard with mouse and rat official nomenclature.
VE:
1 * 100 µl
Lieferant:
Thermo Scientific
Beschreibung:
N-Boc-DL-valin 98%
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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