Sie suchten nach: TLC+EXPLORER

Lieferant: Merck

Beschreibung: 25182537

New Product

Lieferant: Merck

Beschreibung: Überlegene Instrumentenlösung für die zuverlässige TLC-Plattenanalyse. Es kann eine oder mehrere Platten bis zu einer Fläche von 20×20 cm analysieren. Darüber hinaus nutzt das Gerät drei LED-Lichtquellen – weißes Licht (VIS), UV-A (366 nm) und UV-C (254 nm), um die Platten im Direktlichtmodus von oben zu beleuchten. Es ermöglicht eine schnelle visuelle Kontrolle oder eine softwarebasierte Analyse und Quantifizierung.

New Product

Lieferant: ENZO LIFE SCIENCES

Beschreibung: Small molecule STAT3-specific inhibitor which blocks activation, dimerization and nuclear translocation via binding to the STAT3 SH2 domain. It is a very useful tool for exploring STAT3-mediated signaling pathways. It blocks LPS-mediated STAT3 tyrosine phosphorylation which leads to inhibition of LPS-mediated IL-1β and IL-6 production. In primary cultures of rat neural stem cells it blocks IL-15-induced differentiation.

New Product

Lieferant: Molecular Devices

Beschreibung: CatchPoint™ cGMP Fluorescent Assay Kits measure cGMP levels via a competitive immunoassay format. The second messenger cyclic GMP (cGMP) modulates cellular processes, including smooth muscle relaxation, kidney function, and inflammation, by activating effectors such as protein kinases, cGMP-dependent phosphodiesterases, and cGMP-gated ion channels.

Lieferant: Molecular Devices

Beschreibung: CatchPoint™ cAMP Fluorescent Assay Kit measures cAMP levels via a competitive immunoassay format. Cell signaling via G protein-coupled receptors (GPCRs) can be assessed by monitoring the downstream effectors calcium or Cyclic AMP (cAMP). Monitoring levels of cAMP, a second messenger produced in response to activation of adenylate cyclase, is one of the most common ways to screen for agonists and antagonists of GPCRs.

Artikel-Nr: (MLDVR8142)

Lieferant: Molecular Devices

Hersteller Artikel Nummer : R8142

Beschreibung: The FLIPR® Calcium 4 Assay Kit provides a fast, simple and reliable fluorescence-based assay for detecting changes in intracellular calcium.

UOM: 1 * 1 KIT

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Lieferant: LENIOBIO

Beschreibung: ALiCE® - Linearly scalable eukaryotic cell-free protein expression. Scalable protein expression with ALiCE® works as effectively for assessment of future development as it does in the exploration phase. The same simple protocol applies across all scales. Add the DNA sequence and let ALiCE® make your protein.

New Product

Artikel-Nr: (BOSSBS-11993R-HRP)

Lieferant: Bioss

Hersteller Artikel Nummer : BS-11993R-HRP

Beschreibung: Changes in the serine/threonine phosphorylation state of a protein in response to various external stimuli can have profound effects on cellular signal transduction, apoptosis and carcinogenesis. The reagents, including phosphorylated protein/peptides, antibodies against the phosphospecific amino acid, are important tools to explore the activation of serine, threonine or tyrosine containing proteins. An aberrant protein phosphorylation is a hallmark of human disease, and the enzymes, particularly protein kinases, which control protein phosphorylation are recognized as a major new drug target family.

UOM: 1 * 100 µl

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Lieferant: Molecular Devices

Beschreibung: Die FLIPR® Membranpotenzial-Assay-Kits erzeugen homogene fluoreszenzbasierte Rezepturen zur Beobachtung von Veränderungen des Membranpotenzials in Zusammenhang mit der Aktivierung von Ionenkanälen und Ionentransporterproteinen in Echtzeit.

Sicherheitsdatenblätter

Artikel-Nr: (630-3394)

Lieferant: LEICA MICROSYSTEMS

Hersteller Artikel Nummer : 10450921_P1

Beschreibung: Der THUNDER Imager Model Organism ermöglicht eine schnelle und einfache 3D-Erkundung ganzer Organismen (z. B. Drosophila, C. elegans, Zebrafische, Pflanzen und Mäuse) für die Entwicklungs- oder molekularbiologische Forschung. Beseitigen Sie den Ärger mit unscharfen Bildern und behalten Sie gleichzeitig die für Leica-Stereomikroskope typischen Funktionen und die Benutzerfreundlichkeit bei.

UOM: 1 * 1 SET

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Artikel-Nr: (BOSSBS-11993R)

Lieferant: Bioss

Hersteller Artikel Nummer : BS-11993R

Beschreibung: Changes in the serine/threonine phosphorylation state of a protein in response to various external stimuli can have profound effects on cellular signal transduction, apoptosis and carcinogenesis. The reagents, including phosphorylated protein/peptides, antibodies against the phosphospecific amino acid, are important tools to explore the activation of serine, threonine or tyrosine containing proteins. An aberrant protein phosphorylation is a hallmark of human disease, and the enzymes, particularly protein kinases, which control protein phosphorylation are recognized as a major new drug target family.

UOM: 1 * 100 µl

Sale

Artikel-Nr: (BOSSBS-8250R-CY7)

Lieferant: Bioss

Hersteller Artikel Nummer : BS-8250R-CY7

Beschreibung: Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma.

UOM: 1 * 100 µl

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Artikel-Nr: (BOSSBS-8250R-CY5)

Lieferant: Bioss

Hersteller Artikel Nummer : BS-8250R-CY5

Beschreibung: Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma.

UOM: 1 * 100 µl

Sale

Artikel-Nr: (BOSSBS-8362R-CY3)

Lieferant: Bioss

Hersteller Artikel Nummer : BS-8362R-CY3

Beschreibung: Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma.

UOM: 1 * 100 µl

Sale

Artikel-Nr: (BOSSBS-8362R-CY5.5)

Lieferant: Bioss

Hersteller Artikel Nummer : BS-8362R-CY5.5

Beschreibung: Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma.

UOM: 1 * 100 µl

Sale

Artikel-Nr: (BOSSBS-9314R-CY3)

Lieferant: Bioss

Hersteller Artikel Nummer : BS-9314R-CY3

Beschreibung: Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma.

UOM: 1 * 100 µl

Sale