WB
Western blot analysis of lysates from HeLa,NIH/3T3,C6 cells using Phospho-Histone H3-S10 Rabbit mAb at 1:1000 dilution. HeLa,NIH/3T3 and C6 cells were treated with nocodazole (50 ng/mL) at 37℃for 20 hours or treated with CIP(20uL/400ul) at 37℃ for 1 hour.Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) at 1:10000 dilution.Lysates/proteins: 25 μg per lane.Blocking buffer: 3% nonfat dry milk in TBST.Detection: ECL Basic Kit.Exposure time: 1s.ICC/IF
Confocal imaging of C6 cells using PhosphoHistone H3-S10 Rabbit mAb (dilution 1:100) followed by a furtherincubation with Cy3 Goat Anti-Rabbit IgG(H+L) (dilution 1:500) (Red). Thecells were counterstained with α-TubulinMouse mAb (dilution 1:400) followedby incubation with ABflo® 488-conjugatedGoat Anti-Mouse IgG (H+L) Ab (dilution 1:500) (Green). DAPI was used fornuclear staining (Blue). Objective: 100x.ICC/IF
Confocal imaging of HeLa cellsusing Phospho-Histone H3-S10 Rabbit mAb(dilution 1:100) followed by afurther incubation with Cy3 Goat Anti-RabbitIgG (H+L) (dilution 1:500) (Red). Thecells were counterstained with α-TubulinMouse mAb (dilution 1:400) followedby incubation with ABflo® 488-conjugatedGoat Anti-Mouse IgG (H+L) Ab (dilution 1:500) (Green). DAPI was used fornuclear staining (Blue). Objective: 100x.ICC/IF
Confocal imaging of NIH/3T3 cellsusing Phospho-Histone H3-S10 Rabbit mAb(dilution 1:100) followed by afurther incubation with Cy3 Goat Anti-RabbitIgG (H+L) (dilution 1:500) (Red). Thecells were counterstained with α-TubulinMouse mAb (dilution 1:400) followedby incubation with ABflo® 488-conjugatedGoat Anti-Mouse IgG (H+L) Ab (dilution 1:500) (Green). DAPI was used fornuclear staining (Blue). Objective: 100x.IHC
Immunohistochemistry analysis of paraffinembedded Human oophoroma usingPhospho-Histone H3-S10 Rabbit mAb at dilution of 1:100 (40x lens). Highpressure antigen retrieval performed with0.05M Tris/EDTA Buffer (pH 8.0) prior to IHCstaining.IHC
Immunohistochemistry analysis of paraffinembedded Mouse kidney using PhosphoHistone H3-S10 Rabbit mAb at dilution of 1:100 (40x lens). High pressureantigen retrieval performed with 0.05MTris/EDTA Buffer (pH 8.0) prior to IHCstaining.| Product Name | Phospho-Histone H3-S10 Rabbit mAb |
|---|---|
| Antibody Type | Primary Antibodies |
| Immunogen | Synthetic peptide. This information is considered to be commercially sensitive. |
| Modification | P-S10 |
| Clonality | Monoclonal |
|---|---|
| Isotype | IgG |
| Host Species | Rabbit |
| Tested Applications | ICC/IFIHCWB |
| WB:1:500-1:1000 ICC/IF:1:50-1:200 IHC:1:50 - 1:200 |
|
| Species Reactivity | HumanMouseOtherRat |
| Concentration | 1mg/ml |
| Purification | Affinity purified |
| Gene Symbol | H3-4 |
|---|---|
| Gene Synonyms | H3t H3.4 H3/g H3FT H3C16 HIST3H3 |
| Gene Full Name | H3.4 histone, cluster member |
| Gene Summary | Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Nucleosomes consist of approximately 146 bp of DNA wrapped around a histone octamer composed of pairs of each of the four core histones (H2A, H2B, H3, and H4). The chromatin fiber is further compacted through the interaction of a linker histone, H1, with the DNA between the nucleosomes to form higher order chromatin structures. This gene is intronless and encodes a replication-dependent histone that is a member of the histone H3 family. Transcripts from this gene lack polyA tails; instead, they contain a palindromic termination element. This gene is located separately from the other H3 genes that are in the histone gene cluster on chromosome 6p22-p21.3. [provided by RefSeq, Aug 2015] |
| Alternative Names | H3/A H3C2 H3C3 H3C4 H3C6 H3C7 H3C8 H3FA H3C10 H3C11 H3C12 HIST1H3A Phospho-Histone H3-S10 |
| Molecular Weight(MW) | 15kDa(Observed band size:17kDa) |
| Cellular Localization | Chromosome, Nucleus. |
WB
Western blot analysis of lysates from HeLa,NIH/3T3,C6 cells using Phospho-Histone H3-S10 Rabbit mAb at 1:1000 dilution. HeLa,NIH/3T3 and C6 cells were treated with nocodazole (50 ng/mL) at 37℃for 20 hours or treated with CIP(20uL/400ul) at 37℃ for 1 hour.Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) at 1:10000 dilution.Lysates/proteins: 25 μg per lane.Blocking buffer: 3% nonfat dry milk in TBST.Detection: ECL Basic Kit.Exposure time: 1s.
ICC/IF
Confocal imaging of C6 cells using PhosphoHistone H3-S10 Rabbit mAb (dilution 1:100) followed by a furtherincubation with Cy3 Goat Anti-Rabbit IgG(H+L) (dilution 1:500) (Red). Thecells were counterstained with α-TubulinMouse mAb (dilution 1:400) followedby incubation with ABflo® 488-conjugatedGoat Anti-Mouse IgG (H+L) Ab (dilution 1:500) (Green). DAPI was used fornuclear staining (Blue). Objective: 100x.
ICC/IF
Confocal imaging of HeLa cellsusing Phospho-Histone H3-S10 Rabbit mAb(dilution 1:100) followed by afurther incubation with Cy3 Goat Anti-RabbitIgG (H+L) (dilution 1:500) (Red). Thecells were counterstained with α-TubulinMouse mAb (dilution 1:400) followedby incubation with ABflo® 488-conjugatedGoat Anti-Mouse IgG (H+L) Ab (dilution 1:500) (Green). DAPI was used fornuclear staining (Blue). Objective: 100x.
ICC/IF
Confocal imaging of NIH/3T3 cellsusing Phospho-Histone H3-S10 Rabbit mAb(dilution 1:100) followed by afurther incubation with Cy3 Goat Anti-RabbitIgG (H+L) (dilution 1:500) (Red). Thecells were counterstained with α-TubulinMouse mAb (dilution 1:400) followedby incubation with ABflo® 488-conjugatedGoat Anti-Mouse IgG (H+L) Ab (dilution 1:500) (Green). DAPI was used fornuclear staining (Blue). Objective: 100x.
IHC
Immunohistochemistry analysis of paraffinembedded Human oophoroma usingPhospho-Histone H3-S10 Rabbit mAb at dilution of 1:100 (40x lens). Highpressure antigen retrieval performed with0.05M Tris/EDTA Buffer (pH 8.0) prior to IHCstaining.
IHC
Immunohistochemistry analysis of paraffinembedded Mouse kidney using PhosphoHistone H3-S10 Rabbit mAb at dilution of 1:100 (40x lens). High pressureantigen retrieval performed with 0.05MTris/EDTA Buffer (pH 8.0) prior to IHCstaining.| Application Notes | WB:1:500-1:1000 ICC/IF:1:50-1:200 IHC:1:50 - 1:200 |
|---|
| Form | Liquid |
|---|---|
| Storage Instructions | Store at -20℃. Avoid freeze / thaw cycles. |
| Storage Buffer | PBS containing 50% glycerol and 0.05% BSA, preserved with proclin300 or sodium azide (as specified on the Certificate of Analysis), pH 7.3. |
