Sie suchten nach: Antikörper

Entdecken Sie unsere erstklassige Auswahl an Antikörpern, die entwickelt wurden, um wissenschaftliche Entdeckungen in verschiedenen Laboreinstellungen voranzutreiben. Unser umfassender Katalog umfasst monoklonale, polyklonale und rekombinante Antikörper, die jeweils sorgfältig für Anwendungen wie Western Blot, ELISA, Immunchemie und Durchflusszytometrie verifiziert wurden. Passen Sie Ihre Auswahl nach Antigensymbol und -name, Reaktivität, Klonalität, Konjugation und Wirtsart an, um Ihre Forschungsbedürfnisse perfekt zu erfüllen. Verbessern Sie Ihre experimentellen Ergebnisse mit unseren präzisionsgefertigten Antikörpern, die für Genauigkeit und Zuverlässigkeit optimiert sind.

Entdecken Sie unsere erstklassige Auswahl an Antikörpern, die entwickelt wurden, um wissenschaftliche Entdeckungen in verschiedenen Laboreinstellungen voranzutreiben. Unser umfassender Katalog umfasst monoklonale, polyklonale und rekombinante Antikörper, die jeweils sorgfältig für Anwendungen wie Western Blot, ELISA, Immunchemie und Durchflusszytometrie verifiziert wurden. Passen Sie Ihre Auswahl nach Antigensymbol und -name, Reaktivität, Klonalität, Konjugation und Wirtsart an, um Ihre Forschungsbedürfnisse perfekt zu erfüllen. Verbessern Sie Ihre experimentellen Ergebnisse mit unseren präzisionsgefertigten Antikörpern, die für Genauigkeit und Zuverlässigkeit optimiert sind.


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Artikel-Nr: (BOSSBS-11284R-A555)
Lieferant: Bioss
Beschreibung: KSP37 is a 223 amino acid protein that is secreted into the extracellular space and belongs to the fibroblast growth factor-binding protein family. Expressed in serum, as well as in cytotoxic T lymphocytes and peripheral leukocytes, KSP37 is thought to be involved in lymphocyte-mediated immunity, possibly playing a role in the development of asthma. The gene encoding KSP37 maps to human chromosome 4, which encodes nearly 6% of the human genome and has the largest gene deserts (regions of the genome with no protein encoding genes) of all of the human chromosomes. Defects in some of the genes located on chromosome 4 are associated with Huntington's disease, Ellis-van Creveld syndrome, methylmalonic acidemia and polycystic kidney disease.
VE: 1 * 100 µl


Artikel-Nr: (BOSSBS-1850R-A647)
Lieferant: Bioss
Beschreibung: Receptor for both mineralocorticoids (MC) such as aldosterone and glucocorticoids (GC) such as corticosterone or cortisol. Binds to mineralocorticoid response elements (MRE) and transactivates target genes. The effect of MC is to increase ion and water transport and thus raise extracellular fluid volume and blood pressure and lower potassium levels.
VE: 1 * 100 µl


Artikel-Nr: (BOSSBS-6144R-A488)
Lieferant: Bioss
Beschreibung: The protein encoded by this gene is similar to oxidoreductases, which are enzymes involved in cellular responses to oxidative stresses and irradiation. This gene is induced by the tumor suppressor p53 and is thought to be involved in p53-mediated cell death. It contains a p53 consensus binding site in its promoter region and a downstream pentanucleotide microsatellite sequence. P53 has been shown to transcriptionally activate this gene by interacting with the downstream pentanucleotide microsatellite sequence. The microsatellite is polymorphic, with a varying number of pentanucleotide repeats directly correlated with the extent of transcriptional activation by p53. It has been suggested that the microsatellite polymorphism may be associated with differential susceptibility to cancer. At least two transcript variants encoding the same protein have been found for this gene (from EntrezGene).
VE: 1 * 100 µl


Artikel-Nr: (BOSSBS-6851R-A680)
Lieferant: Bioss
Beschreibung: The protein encoded by this gene catalyzes the O-sulfation of tyrosine residues within acidic regions of proteins. The encoded protein is a type II integral membrane protein found in the Golgi body. Two transcript variants encoding the same protein have been found for this gene.
VE: 1 * 100 µl


Artikel-Nr: (BOSSBS-13299R-A750)
Lieferant: Bioss
Beschreibung: NIPSNAP2 is a 286 amino acid protein that is abundantly expressed in heart and skeletal muscle. Belonging to the NIPSNAP family, NIPSNAP2 may be involved in vesicular transport. NIPSNAP2 contains a signal peptide, a transmembrane domain and two tyrosine phosphorylation sites. NIPSNAP2 is encoded by a gene mapping to human chromosome 7p11.2. Chromosomal region 7p12 is amplified in approximately 40% of glioblastomas, the most common and malignant form of central nervous system tumor. Human chromosome 7 houses over 1,000 genes and comprises nearly 5% of the human genome. Defects in some of the genes localized to chromosome 7 have been linked to Osteogenesis imperfecta, Williams-Beuren syndrome, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome.
VE: 1 * 100 µl


Artikel-Nr: (BOSSBS-1178R-A555)
Lieferant: Bioss
Beschreibung: Coagulation factor II (thrombin) receptor-like 1 (F2RL1) is a member of the large family of 7-transmembrane-region receptors that couple to guanosine-nucleotide-binding proteins. F2RL1 is also a member of the protease-activated receptor family. It is activated by trypsin, but not by thrombin. It is activated by proteolytic cleavage of its extracellular amino terminus. The new amino terminus functions as a tethered ligand and activates the receptor. The F2RL1 gene contains two exons and is widely expressed in human tissues. The predicted protein sequence is 83% identical to the mouse receptor sequence. [provided by RefSeq, Jul 2008]
VE: 1 * 100 µl


Artikel-Nr: (BOSSBS-3034R-A750)
Lieferant: Bioss
Beschreibung: This is the catalytic component of the active enzyme, which catalyses the hydrolysis of ATP coupled with the exchange of sodium and potassium ions across the plasma membrane. This action creates the electrochemical gradient of sodium and potassium ions, providing the energy for active transport of various nutrients.
VE: 1 * 100 µl


Artikel-Nr: (BOSSBS-5751R-A750)
Lieferant: Bioss
Beschreibung: The protein encoded by this gene has amino acid sequence similarity to Csk tyrosine kinase and has the structural features of the CSK subfamily: SRC homology SH2 and SH3 domains, a catalytic domain, a unique N terminus, lack of myristylation signals, lack of a negative regulatory phosphorylation site, and lack of an autophosphorylation site. MATK is thought to play a significant role in the signal transduction of hematopoietic cells. It is able to phosphorylate and inactivate Src family kinases, and may play an inhibitory role in the control of T-cell proliferation. This protein might be involved in signaling in some cases of breast cancer.
VE: 1 * 100 µl


Artikel-Nr: (BOSSBS-8239R-A680)
Lieferant: Bioss
Beschreibung: No data available.
VE: 1 * 100 µl


Lieferant: Biotium
Beschreibung: CD3e (Clone SK7) is a mouse monoclonal antibody derived from the extracellular domain of the CD3 epsilon chain. This antibody belongs to the Biotium Choice list of select antibodies that have been validated and optimized in-house for optimal performance. The antibody is available conjugated to either a CF® Dye or Astral™ tandem dye. They are supplied in PBS, 0,1% BSA, 0,05% azide.

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Artikel-Nr: (BOSSBS-9703R-A647)
Lieferant: Bioss
Beschreibung: Hornerin has similar structural features to those of profilaggrin, an essential protein for keratinization of epidermal tissues. Hornerin may play a role in cornification.
VE: 1 * 100 µl


Artikel-Nr: (BOSSBS-8117R-A350)
Lieferant: Bioss
Beschreibung: CCDC146
VE: 1 * 100 µl


Artikel-Nr: (BOSSBS-12928R-A488)
Lieferant: Bioss
Beschreibung: The cytochrome P450 proteins (CYPs) are monooxygenases that catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids, and other lipids. P450 enzymes are classified into subfamilies based on their sequence similarities. CYP26A1 is a major retinoic acid catabolic enzyme. CYP26A1 plays an important role in protecting tailbud tissues from inappropriate exposure to retinoic acid. CYP26A1 transcription is epigenetically regulated by nuclear retinoic acid receptor ∫2. Mutations in the gene encoding for CYP26A1 are associated with caudal agenesis and spina bifida, imperforate anus, agenesis of the caudal portions of the digestive and urogenital tracts, and malformed lumbosacral skeletal elements. CYP26A1 is upregulated in adenomatous polyposis coli mouse adenomas, human FAP adenomas, human sporadic colon carcinomas, and in the intestine of adenomatous polyposis coli (apcmcr) mutant zebrafish embryos.
VE: 1 * 100 µl


Artikel-Nr: (BOSSBS-1857R-A750)
Lieferant: Bioss
Beschreibung: The product of this gene belongs to the family of G-protein coupled receptors. This family has several receptor subtypes with different pharmacological selectivity, which overlaps in some cases, for various adenosine and uridine nucleotides. This receptor is responsive to uridine nucleotides, partially responsive to ATP, and not responsive to ADP. P2Y4 expression has been documented in blood, bone, heart, lung, pancreas, placenta, and umbilical cord.
VE: 1 * 100 µl


Artikel-Nr: (BOSSBS-12465R-A555)
Lieferant: Bioss
Beschreibung: Syntaxins were originally thought to be docking proteins, but have more recently been categorized as anchoring proteins that anchor themselves to the cytoplasmic surfaces of cellular membranes. Syntaxins have been shown to bind to various proteins involved in exocytosis, including VAMPs (vesicle-associated membrane proteins), NSF (N-ethylmaleimide-sensitive factor), SNAP 25 (synaptosomal-associated protein of 25kDa), SNAPs (soluble NSF attachment proteins) and synaptotagmin. VAMPs (also designated synaptobrevins), including VAMP-1 and VAMP-2, and synaptotagmin, a protein that may function as an inhibitor of exocytosis, are vesicular proteins.
VE: 1 * 100 µl


Artikel-Nr: (AGRIAS111820)
Lieferant: Agrisera
Beschreibung: Anti-IgY Goat Polyclonal Antibody (DyLight® 350)
VE: 1 * 1 mg


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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 call noch angezeigt wird und Sie Hilfe benötigen, rufen Sie uns an 1-800-932 - 5000.
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