HDAC1 Rabbit Monoclonal Antibody(ARA781)
WB | 1:1000-1:2000 |
IHC | 1:100-1:200 |
IF/ICC | 1:200-1:500 |
Description | Rabbit Monoclonal Antibody to HDAC1 |
Antibody Type | Primary antibody |
Predicted MW | 55kDa |
Immunogen | A synthetic peptide corresponding to the C-term of HDAC1 was used as an immunogen. |
Purification | ProA affinity purified IgG |
Form/Buffer | PBS 59%, Sodium azide 0.01%, Glycerol 40%, BSA 0.56%. |
Alternative Names | RPD3L1; Histone deacetylase 1; HD1 |
Gene Symbol | HDAC1 |
Entrez Gene | 3065(Human); 297893(Rat) |
Swissprot | Q13547 |
*Clone Number, Reactivity, Source/Host and Clonality can be found in the product name and Key Features section above.

All lanes: Anti-HDAC1 antibody at 1:1,000 dilution
Predicted MW: 55 kDa
Observed MW: 65 kDa
Lane 1: Jurkat
Lane 2: K562
Lane 3: Molt-4
Lysate at 10 µg per lane
2nd Ab:
GAR HRP(H+L) 1:5,000
Exposure: 20s

All lanes: Anti-HDAC1 antibody at 1:1,000 dilution
Predicted MW: 55 kDa
Observed MW: 65 kDa
Lane 1: MDBK
Lane 2: COS-7
Lysate at 10 µg per lane
2nd Ab:
GAR HRP(H+L) 1:5,000
Exposure: 60s

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) analysis human colon tissue labelling HDAC1 with ARA781 at 1:200. Heat mediated antigen retrieval was performed using Tris/EDTA buffer pH 9.0.

ARA781 staining HDAC1 in Hela cells by IF/ICC (immunofluorescence/immunocytochemistry). Cells were fixed with paraformaldehyde, permeabilized with 0.1% Triton X-100 and blocked with 10% goat serum for half an hour at room temperature. Samples were incubated with primary antibody (1:500) at 4°C. An Alexa Fluor<sup>®</sup> 594-conjugated Goat Anti-Rabbit IgG polyclonal was used as the secondary antibody (1:500). DAPI (blue) was used as the nuclear counter stain.
Control: PBS and secondary antibody, An Alexa Fluor<sup>®</sup> 594-conjugated Goat Anti-Rabbit IgG (1:500).

Overlay histogram showing Hela cells stained with ARA781 (Red). The cells were fixed with 4% paraformaldehyde (10 min) and then permeabilized with 0.1% TritonX-100 for 15 min. The cells were then incubated in the antibody (ARA781, 1:200 dilution) in 1x PBS/1% BSA for 30 min at room temperature. The secondary antibody used was a Goat Anti-Rabbit Alexa Fluor<sup>®</sup> 488 (IgG H+L) at 1:2,000 dilution for 20 min at room temperature. Unlabelled sample (Black) was used as a control.
FAQs
New Products
Datasheet
