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Potassium+trifluoro(hex-1-yn-1-yl)borate
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Potassium+trifluoro(hex-1-yn-1-yl)borate
Artikel-Nr:
(BOSSBS-5951R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5951R
Lokale Artikelnummer::
BOSSBS-5951R
Beschreibung:
Effector of integrin and growth factor signaling, coupling surface receptors to downstream signaling molecules involved in the regulation of cell survival, cell proliferation and cell differentiation. Focal adhesion protein part of the complex ILK-PINCH. This complex is considered to be one of the convergence points of integrin- and growth factor-signaling pathway.
VE:
1 * 100 µl
Artikel-Nr:
(BOHLR1127-04)
Lieferant:
Bohlender
Hersteller-Artikelnummer::
R1127-04
Lokale Artikelnummer::
BOHLR1127-04
Beschreibung:
Sammelanschluss für bis zu vier HPLC-Anlagen, der direkt in Laborabzüge oder Arbeitstische integriert werden kann. Mit b.safe Waste Pipes leiten Sie flüssige Lösemittelabfälle in angeschlossene Kanister weiter.
VE:
1 * 1 ST
Artikel-Nr:
(BOSSBS-3769R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-3769R-A350
Lokale Artikelnummer::
BOSSBS-3769R-A350
Beschreibung:
Modulation of the chromatin structure plays an important role in the regulation of transcription in eukaryotes. The nucleosome, made up of four core histone proteins (H2A, H2B, H3 and H4), is the primary building block of chromatin. The N-terminal tail of core histones undergoes different posttranslational modifications including acetylation, phosphorylation and methylation. These modifications occur in response to cell signal stimuli and have a direct effect on gene expression. In most species, the histone H2B is primarily acetylated at lysines 5, 12, 15 and 20. Histone H3 is primarily acetylated at lysines 9, 14, 18 and 23. Acetylation at lysine 9 appears to have a dominant role in histone deposition and chromatin assembly in some organisms. Phosphorylation at Ser10 of histone H3 is tightly correlated with chromosome condensation during both mitosis and meiosis.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8091R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8091R
Lokale Artikelnummer::
BOSSBS-8091R
Beschreibung:
Required for assembly of dynein regulatory complex (DRC) and inner dynein arm complexes, which are responsible for ciliary beat regulation, thereby playing a central role in motility in cilia and flagella. Not required for outer dynein arm complexes assembly. Required for axonemal recruitment of CCDC39.Involvement in disease:Defects in CCDC40 are the cause of primary ciliary dyskinesia type 15 (CILD15) . A disorder characterized by abnormalities of motile cilia. Respiratory infections leading to chronic inflammation and bronchiectasis are recurrent, due to defects in the respiratory cilia; reduced fertility is often observed in male patients due to abnormalities of sperm tails. Half of the patients exhibit randomization of left-right body asymmetry and situs inversus, due to dysfunction of monocilia at the embryonic node. Primary ciliary dyskinesia associated with situs inversus is referred to as Kartagener syndrome.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-3769R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-3769R-FITC
Lokale Artikelnummer::
BOSSBS-3769R-FITC
Beschreibung:
Modulation of the chromatin structure plays an important role in the regulation of transcription in eukaryotes. The nucleosome, made up of four core histone proteins (H2A, H2B, H3 and H4), is the primary building block of chromatin. The N-terminal tail of core histones undergoes different posttranslational modifications including acetylation, phosphorylation and methylation. These modifications occur in response to cell signal stimuli and have a direct effect on gene expression. In most species, the histone H2B is primarily acetylated at lysines 5, 12, 15 and 20. Histone H3 is primarily acetylated at lysines 9, 14, 18 and 23. Acetylation at lysine 9 appears to have a dominant role in histone deposition and chromatin assembly in some organisms. Phosphorylation at Ser10 of histone H3 is tightly correlated with chromosome condensation during both mitosis and meiosis.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8091R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8091R-HRP
Lokale Artikelnummer::
BOSSBS-8091R-HRP
Beschreibung:
Required for assembly of dynein regulatory complex (DRC) and inner dynein arm complexes, which are responsible for ciliary beat regulation, thereby playing a central role in motility in cilia and flagella. Not required for outer dynein arm complexes assembly. Required for axonemal recruitment of CCDC39.Involvement in disease:Defects in CCDC40 are the cause of primary ciliary dyskinesia type 15 (CILD15) . A disorder characterized by abnormalities of motile cilia. Respiratory infections leading to chronic inflammation and bronchiectasis are recurrent, due to defects in the respiratory cilia; reduced fertility is often observed in male patients due to abnormalities of sperm tails. Half of the patients exhibit randomization of left-right body asymmetry and situs inversus, due to dysfunction of monocilia at the embryonic node. Primary ciliary dyskinesia associated with situs inversus is referred to as Kartagener syndrome.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8091R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8091R-FITC
Lokale Artikelnummer::
BOSSBS-8091R-FITC
Beschreibung:
Required for assembly of dynein regulatory complex (DRC) and inner dynein arm complexes, which are responsible for ciliary beat regulation, thereby playing a central role in motility in cilia and flagella. Not required for outer dynein arm complexes assembly. Required for axonemal recruitment of CCDC39.Involvement in disease:Defects in CCDC40 are the cause of primary ciliary dyskinesia type 15 (CILD15) . A disorder characterized by abnormalities of motile cilia. Respiratory infections leading to chronic inflammation and bronchiectasis are recurrent, due to defects in the respiratory cilia; reduced fertility is often observed in male patients due to abnormalities of sperm tails. Half of the patients exhibit randomization of left-right body asymmetry and situs inversus, due to dysfunction of monocilia at the embryonic node. Primary ciliary dyskinesia associated with situs inversus is referred to as Kartagener syndrome.
VE:
1 * 100 µl
Lieferant:
Bernd Kraft
Beschreibung:
Ammoniaklösung 15% analytisches Reagens
Artikel-Nr:
(TNB-6600-KIT)
Lieferant:
Tonbo Biosciences
Hersteller-Artikelnummer::
TNB-6600-KIT
Lokale Artikelnummer::
TNBOTNB-6600-KIT
Beschreibung:
The fragmentation of genomic DNA by cellular nucleases during the later stages of apoptosis is also one of the most easily measured features of apoptotic cells. Nuclease activity generates DNA fragments ranging from ~300 bp to 50 bp in length, resulting in a typical DNA ‘laddering’ appearance when analyzed by agarose gel electrophoresis. These fragments have exposed 3’-hydroxyl (OH) ends which can be labeled with bromolated deoxyuridine triphosphates (Br-dUTP). An enzyme, terminal deoxynucleotidyl transferase (TdT), is used to catalyze the template-independent addition of Br-dUTP to the 3’-OH ends of double or single stranded DNA. This method is often called TUNEL (terminal deoxynucleotidyl transferase dUTP nick end labeling) or end labeling. Sites where the Br-dUTP is incorporated can then be detected with an antibody specific to BrdU. With the APO-BrdUTM Kit cells are first labeled with Br-dUTP, and then sites of incorporation are detected through staining with a FITC anti-BrdU antibody. Samples can then be analyzed via flow cytometry. Samples that are apoptotic will stain brightly with the anti-BrdU antibody due to the substantial number of exposed 3’-OH sites, while cells that are non-apoptotic will not have incorporated significant amounts of Br-dUTP and will stain dimly. The APO-BrdU Kit is shipped in one container and consists of two packages. Upon arrival one should be stored at 2-8°C and the other at -20°C.
VE:
1 * 50 Tests
Lieferant:
ACROBIOSYSTEMS
Beschreibung:
Human Siglec-15 / CD33L3 Protein, His Tag.
Lieferant:
ENTEGRIS
Beschreibung:
H 22 Serie
Fasst einen Wafer mit aktiver Seite nach unten, wobei nur die Kanten des Wafers berührt werden.
Lieferant:
ECONIX
Beschreibung:
These stands for 6 litre Bio-bin® waste disposal boxes are made from stainless steel.
Artikel-Nr:
(BOSSBS-4289R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-4289R-A647
Lokale Artikelnummer::
BOSSBS-4289R-A647
Beschreibung:
This is one of the several different receptors for 5-hydroxytryptamine (serotonin), a biogenic hormone that functions as a neurotransmitter, a hormone, and a mitogen. This receptor is a ligand-gated ion channel, which when activated causes fast, depolarizing responses. It is a cation-specific, but otherwise relatively nonselective, ion channel.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-7983R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-7983R-A647
Lokale Artikelnummer::
BOSSBS-7983R-A647
Beschreibung:
The protein encoded by this gene is one of several isozymes of carbonic anhydrase. This protein is found only in salivary glands and saliva and protein may play a role in the reversible hydratation of carbon dioxide though its function in saliva is unknown. [provided by RefSeq, Jul 2008].
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-4289R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-4289R-A350
Lokale Artikelnummer::
BOSSBS-4289R-A350
Beschreibung:
This is one of the several different receptors for 5-hydroxytryptamine (serotonin), a biogenic hormone that functions as a neurotransmitter, a hormone, and a mitogen. This receptor is a ligand-gated ion channel, which when activated causes fast, depolarizing responses. It is a cation-specific, but otherwise relatively nonselective, ion channel.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9980R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9980R-A680
Lokale Artikelnummer::
BOSSBS-9980R-A680
Beschreibung:
The smallest of the human chromosomes, 21 makes up about 1.5% of the human genome. Chromosome 21 contains nearly 300 genes and 47 million base pairs. Down syndrome, also known as trisomy 21, is the disease most commonly associated with chromosome 21. Alzheimer's disease, Jervell and Lange-Nielsen syndrome and amyotrophic lateral sclerosis are also associated with chromosome 21. Translocations are found to occur between chromosome 21 and 8, and chromosome 21 and 12, in certain leukaemias. DnaJC28 (DnaJ homolog subfamily C member 28), also known as C21orf55, C21orf78 or MGC27620 is a 388 amino acid protein that is expressed in the fetal and adult brain, testis, uterus, spleen and liver. It has been suggested that DnaJC28 may play a role in protein folding or as a chaperone. The DnaJC28 gene product has been provisionally designated DnaJC28 pending further characterisation.
VE:
1 * 100 µl
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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