6His-tagged fusion protein corresponding to residues 1031-1215 of human histone deacetylase 6 (HDAC6).
Application
Anti-HDAC6 Antibody, CT is a Rabbit Polyclonal Antibody for detection of HDAC6 also known as histone deacetylase 6 & has been tested in IP & WB.
Research Category Epigenetics & Nuclear Function
Research Sub Category Histones
Quality
Routinely evaluated by immunoblot.
Target description
134kDa
Linkage
Replaces: MABE546
Physical form
Format: Purified
Protein A purified
Storage and Stability
2 years at -20°C from date of shipment
Analysis Note
Control Positive Antigen Control: Catalog #12-303, Jurkat cell lysate.
Legal Information
UPSTATE is a registered trademark of Merck KGaA, Darmstadt, Germany
Disclaimer
Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
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Storage Class
10 - Combustible liquids
wgk_germany
WGK 1
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
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Epigenetic status determines germ cell meiotic commitment in embryonic and postnatal mammalian gonads.
Wang, N; Tilly, JL
Cell Cycle null
Upregulation of miR-22 promotes osteogenic differentiation and inhibits adipogenic differentiation of human adipose tissue-derived mesenchymal stem cells by repressing HDAC6 protein expression.
Homer2 deletion alters dendritic spine morphology but not alcohol-associated adaptations in GluN2B-containing N-methyl-D-aspartate receptors in the nucleus accumbens.
Fibrotic cataract, including posterior capsule opacification (PCO) and anterior subcapsular cataract (ASC), renders millions of people visually impaired worldwide. However, the underlying mechanism remains poorly understood. Here, we report a miRNA-based regulatory pathway that controls pathological fibrosis of lens epithelium.
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