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Host: Rabbit
Target Protein: Histone H3 (Acetyl K23)
Specificity: This acetylation site is homologous across the species listed.
Modification Site: K23
Clonality: Polyclonal
Isotype: IgG
Entrez Gene: 3020
Swiss Prot: P84243
Source: KLH conjugated synthetic acetylpeptide derived from human Histone H3 around acetylation site of Lys23
Purification: Purified by Protein A.
Storage Buffer: 0.01M TBS(pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
Storage: Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
Background:
Size: 100ul
Concentration: 1ug/ul
Applications:
ELISA(1:500-1000)
FCM(1:20-100)
IHC-P(1:200-400)
IHC-F(1:100-500)
IF(IHC-P)(1:50-200)
IF(IHC-F)(1:50-200)
IF(ICC)(1:50-200)
Predicted Molecular Weight: 15
Cross Reactive Species:
Human
Mouse
Rat
Predicted Cross Reactive Species:
Cow
Pig
Rabbit
Fruit Fly
For research use only. Not intended for diagnostic or therapeutic use.
Formalin-fixed and paraffin embedded mouse spleen labeled with Anti Acetyl-Histone H3 Polyclonal Antibody, Unconjugated (bs-3774R) at 1:200 followed by conjugation to the secondary antibody and DAB staining
Paraformaldehyde-fixed, paraffin embedded Rat liver; Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15min; Block endogenous peroxidase by 3% hydrogen peroxide for 20 minutes; Blocking buffer (normal goat serum) at 37°C for 30min; Antibody incubation with Acetyl Histone H3(K23) Polyclonal Antibody, Unconjugated (bs-3774R) at 1:400 overnight at 4°C, DAB staining.
Hela cells were fixed with 70% ice-cold methanol overnight at 4℃，permeabilized with 90% ice-cold methanol for 20 min at -20℃, and incubated in 5% BSA blocking buffer for 30 min at room temperature. Cells were then stained with Acetyl Histone H3(K23)Antibody(bs-3774R) at 1：50dilution in blocking buffer and incubated for 30 min at room temperature, washed twice with 2%BSA in PBS, followed by secondary antibody incubation for 40 min at room temperature. Acquisitions of 20,000 events were performed. Cells stained with primary antibody (green), no antibody control control (blue), secondary antibody only (light blue) and isotype control (orange).
Paraformaldehyde-fixed, paraffin embedded Rat pancreas; Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15min; Block endogenous peroxidase by 3% hydrogen peroxide for 20 minutes; Blocking buffer (normal goat serum) at 37°C for 30min; Antibody incubation with Acetyl Histone H3(K23) Polyclonal Antibody, Unconjugated (bs-3774R) at 1:200 overnight at 4°C, DAB staining.
Paraformaldehyde-fixed, paraffin embedded Mouse pancreas; Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15min; Block endogenous peroxidase by 3% hydrogen peroxide for 20 minutes; Blocking buffer (normal goat serum) at 37°C for 30min; Antibody incubation with Acetyl Histone H3(K23) Polyclonal Antibody, Unconjugated (bs-3774R) at 1:200 overnight at 4°C, DAB staining.
4% Paraformaldehyde-fixed Hela (treated with 500 ng/ml Trichostatin A for 4 h) (H) cell; Triton X-100 at r.t. for 20 min; Antibody incubation with (Histone H3 (Acetyl K23)) polyclonal Antibody, unconjugated (bs-3774R) 1:100, 90 min at 37°C; followed by conjugated Goat Anti-Rabbit IgG antibody (green, bs-40295G-FITC) at 37°C for 90 min, DAPI (blue, C02-04002) was used to stain the cell nuclei. PBS instead of the primary antibody was used as the blank control.