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.
Anti-CTPS2 Rabbit Polyclonal Antibody
Supplier: Abcam
Rabbit Polyclonal CTPS2 antibody. C-terminal. Suitable for IP, WB and reacts with Human samples. Cited in 1 publication. Immunogen corresponding to Synthetic Peptide within Human CTPS2 aa 500 to C-terminus.
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Anti-C18orf56 Rabbit Polyclonal Antibody
Supplier: Bioss
Encoding over 300 genes, chromosome 18 contains about 76 million bases. Trisomy 18, or Edwards syndrome, is the second most common trisomy after Downs syndrome. Symptoms of Edwards syndrome include low birth weight, a variety of physical development defects, heart deformations and breathing difficulty. Translocation between chromosome 18 and 14 is the most common translocation in cancers, and occurs in follicular lymphomas. Niemann-Pick disease, hereditary hemorrhagic telangiectasia and erythropoietic protoporphyria are associated with chromosome 18. The TGFβ modulators, Smad2, Smad4 and Smad7 are encoded by chromosome 18. The C18orf56 gene product has been provisionally designated C18orf56 pending further characterization.
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Anti-FANCG Rabbit Polyclonal Antibody (Cy5®)
Supplier: Bioss
FANCG, involved in Fanconi anemia, confers resistance to both hygromycin and mitomycin C. FANCG contains a 5-prime GC-rich untranslated region characteristic of housekeeping genes. The putative 622-amino acid protein has a leucine-zipper motif at its N-terminus. Fanconi anemia is an autosomal recessive disorder with diverse clinical symptoms, including developmental anomalies, bone marrow failure, and early occurrence of malignancies. A minimum of 8 FA genes have been identified.
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Anti-HTR7 Rabbit Polyclonal Antibody
Supplier: Novus Biologicals
Anti-HTR7 Rabbit Polyclonal Antibody
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Anti-LY6G6D Rabbit Polyclonal Antibody
Supplier: US Biological
Anti-LY6G6D Rabbit Polyclonal Antibody
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Anti-Solute Carrier Family 5 Rabbit Polyclonal Antibody
Supplier: US Biological
Anti-Solute Carrier Family 5 Rabbit Polyclonal Antibody
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Anti-Claudin 10 Rabbit Polyclonal Antibody (Cy7®)
Supplier: Bioss
The claudin superfamily consists of many structurally related proteins in humans. These proteins are important structural and functional components of tight junctions in paracellular transport. Claudins are located in both epithelial and endothelial cells in all tight junction-bearing tissues. Three classes of proteins are known to localize to tight junctions, including the claudins, Occludin and junction adhesion molecules. Claudins, which consist of four transmembrane domains and two extracellular loops, make up tight junction strands. Claudin expression is often highly restricted to specfic regions of different tissues and may have an important role in transcellular transport through tight junctions. Claudin-10 is a 228 amino acid multi-pass membrane protein that belongs to the claudin family and plays an important role in cell-adhesion activity and tight junction-specific events.
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Anti-MSRB3 Rabbit Monoclonal Antibody [clone: EPR13664]
Supplier: Abcam
Rabbit recombinant monoclonal MSRB3 antibody. Suitable for WB and reacts with Human samples. Cited in 2 publications.
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Anti-CTF18 Rabbit Polyclonal Antibody
Supplier: Abcam
Rabbit Polyclonal CTF18 antibody. Suitable for WB, ICC/IF and reacts with Human samples. Immunogen corresponding to Recombinant Fragment Protein within Human CHTF18 aa 850 to C-terminus.
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Anti-MSN Mouse Monoclonal Antibody (Biotin) [clone: MSN493]
Supplier: Biotium
Recognizes 78 kDa moesin protein. Moesin, a member of the talin-4.1 superfamily, is a linking protein of the sub-membranous actin cytoskeleton. It is expressed in variable amounts in cells of different phenotypes such as macrophages, lymphocytes, fibroblastic, endothelial, epithelial, and neuronal cell lines but not in blood cells. The ERM proteins, ezrin, radixin, and moesin are involved in a variety of cellular functions, such as cell adhesion, migration, and the organization of cell surface structures, and are highly homologous, both in protein sequence and in functional activity, with merlin/schwannomin, a neurofibromatosis-2-associated tumor-suppressor protein. Cell lines of epithelial and mesothelial origin contain both moesin and radixin whereas cells of endothelial and lymphoid origin express moesin.
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Anti-FbxO6 Rabbit Polyclonal Antibody
Supplier: Abcam
Rabbit Polyclonal FbxO6 antibody. Suitable for WB, IHC-P and reacts with Human samples. Cited in 2 publications. Immunogen corresponding to Synthetic Peptide within Human FBXO6 aa 1 to C-terminus.
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Anti-EFEMP1 Rabbit Polyclonal Antibody
Supplier: US Biological
Anti-EFEMP1 Rabbit Polyclonal Antibody
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Anti-NAMPT Rabbit Polyclonal Antibody
Supplier: US Biological
Anti-NAMPT Rabbit Polyclonal Antibody
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Anti-p-MAX Rabbit Polyclonal Antibody [clone: S11]
Supplier: Bioworld Technology
Synthetic phosphopeptide derived from human MAX around the phosphorylation site of Serine 11.
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Anti-ERMN Rabbit Polyclonal Antibody
Supplier: US Biological
Anti-ERMN Rabbit Polyclonal Antibody
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Anti-IQCJ Rabbit Polyclonal Antibody (Cy7®)
Supplier: Bioss
IQCJ (IQ domain-containing protein J) is a 159 amino acid protein that contains one IQ domain. Existing as four alternatively spliced isoforms, the gene encoding IQCJ maps to human chromosome 3q25.32. Chromosome 3 houses over 1,100 genes, including a chemokine receptor (CKR) gene cluster and a variety of human cancer-related gene loci. Key tumor suppressing genes on chromosome 3 include those that encode the apoptosis mediator RASSF1, the cell migration regulator HYAL1 and the angiogenesis suppressor SEMA3B. Marfan Syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth Disease are a few of the numerous genetic diseases associated with chromosome 3.



