H1F0 (Ab-101) Antibody, Unconjugated, Rabbit, Polyclonal
Artikelnummer:
CSB-PA010087OA101NME1HU
- Bilder (4)
| Artikelname: | H1F0 (Ab-101) Antibody, Unconjugated, Rabbit, Polyclonal |
| Artikelnummer: | CSB-PA010087OA101NME1HU |
| Hersteller Artikelnummer: | CSB-PA010087OA101nme1HU |
| Alternativnummer: | CSB-PA010087OA101NME1HU-100UL, CSB-PA010087OA101NME1HU-50UL |
| Hersteller: | Cusabio |
| Wirt: | Rabbit |
| Kategorie: | Antikörper |
| Applikation: | ChIP, ELISA, IF, IHC, WB |
| Spezies Reaktivität: | Human, Rat |
| Konjugation: | Unconjugated |
| Alternative Synonym: | H1 histone family member 0 antibody, H1(0) antibody, H10 antibody, H10_HUMAN antibody, h1f0 antibody, H1FV antibody, Histone H1 antibody, Histone H1(0) antibody, Histone H1.0 antibody, Histone H10 antibody, Histone H5 antibody, MGC5241 antibody, N-terminally processed antibody |
| Klonalität: | Polyclonal |
| UniProt: | P07305 |
| Puffer: | Preservative: 0.03% Proclin 300<br />Constituents: 50% Glycerol, 0.01M PBS, pH 7.4 |
| Reinheit: | Antigen Affinity Purified |
| Formulierung: | Liquid |
| Target-Kategorie: | H1F0 |
| Application Verdünnung: | Recommended dilution: WB:1:50-1:500, IHC:1:20-1:200, IF:1:1-1:10 |
|
|
Chromatin Immunoprecipitation Hela (4*106) were treated with Micrococcal Nuclease, sonicated, and immunoprecipitated with 5µg anti-H1F0 (CSB-PA010087OA101nme1HU) or a control normal rabbit IgG. The resulting ChIP DNA was quantified using real-time PCR with primers against the beta-Globin promoter. |
|
|
Immunofluorescence staining of HepG2 cells with CSB-PA010087OA101nme1HU at 1:1, counter-stained with DAPI. The cells were fixed in 4% formaldehyde, permeabilized using 0.2% Triton X-100 and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4°,C. The secondary antibody was Alexa Fluor 488-congugated AffiniPure Goat Anti-Rabbit IgG(H+L). |
|
|
IHC image of CSB-PA010087OA101nme1HU diluted at 1:50 and staining in paraffin-embedded human melanoma performed on a Leica BondTM system. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4°,C overnight. The primary is detected by a biotinylated secondary antibody and visualized using an HRP conjugated SP system. |
|
|
Western Blot Positive WB detected in: Rat spleen tissue All lanes: H1F0 antibody at 0.85µg/ml Secondary Goat polyclonal to rabbit IgG at 1/50000 dilution Predicted band size: 21, 20 kDa Observed band size: 21 kDa |
Produktgarantie und fachkundiger Support
