Immunohistochemistry-Paraffin: ZFX Antibody [NBP1-80583] - Staining of human cerebellum shows moderate nuclear positivity in cells in granular layer.
Immunohistochemistry-Paraffin: ZFX Antibody [NBP1-80583] - Human duodenum shows moderate nuclear positivity in glandular cells.
Immunohistochemistry-Paraffin: ZFX Antibody [NBP1-80583] - Staining of human endometrium shows moderate nuclear positivity in glandular cells.
Immunohistochemistry-Paraffin: ZFX Antibody [NBP1-80583] - Staining of human testis shows weak to moderate nuclear positivity in cells in seminiferous ducts.
Immunohistochemistry-Paraffin: ZFX Antibody [NBP1-80583] - Staining of human skeletal muscle shows no positivity in myocytes as expected.
Recombinant Protein Epitope Signature Tag (PrEST) antigen sequence: IGPDGHPLTVYPCMICGKKFKSRGFLKRHMKNHPEHLAKKKYHCTDCDYTTNKKISLHNHLESHKLTSKAEKAIECDECGKHFSHAGALFTHKMVHKEKGANKMHKCKFCEYETAEQGLLNRHL
Predicted Species
Mouse (99%), Rat (99%). Backed by our 100% Guarantee.
Isotype
IgG
Clonality
Polyclonal
Host
Rabbit
Gene
ZFX
Purity
Immunogen affinity purified
Innovator's Reward
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Store at 4C short term. Aliquot and store at -20C long term. Avoid freeze-thaw cycles.
Buffer
PBS (pH 7.2) and 40% Glycerol
Preservative
0.02% Sodium Azide
Purity
Immunogen affinity purified
Alternate Names for ZFX Antibody - BSA Free
zinc finger protein, X-linked
Background
Chimera RNA interference (chimera RNAi) is process by which small interfering RNA/DNA chimera triggers the destruction of mRNA for the original gene. The discovery work, design, and application of chimera RNAi has been pioneered by Professor Kaoru Saigo and Dr. Kumiko Ui-Tei at the University of Tokyo. Chimera RNAi has many advantages over the conventional siRNAs. First, it has been demonstrated to have reliable knock-down for over 10,000 human genes. Because the human genome is composed of an intricate, genetic network, chimera RNAi's unique design has successfully obviated the off-target effects including microRNA-based influence. Another advantage of the chimera RNAi technology is its effectiveness at low concentrations (0.5nM to 5nM); only mRNA is destroyed so genomic genes are not affected. Finally, having both the sense and anti-sense strands consisting RNA/DNA chimera, it offers much greater compound stability for streamlining in vitro and in vivo assays and applications while minimizing interferon induction and other adverse reactions.
Limitations
This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.
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