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Phospho-Histone H3-S10 Rabbit mAb (AP0002)

Review (1)Publications (4) Datasheet

Tested applications:WBIHC-PIF/ICCIPChIPChIP-seqRIPFCFC(Intra)ELISAMeDIPNucleotide ArrayDBFACSCoIPCUT&TagmeRIPInhibitionReactivity:Human, Mouse, Rat, Other (Wide Range Predicted)

ABclonal:Western blot - Phospho-Histone H3-S10 Rabbit mAb (AP0002)

Western blot analysis of lysates from HeLa, NIH/3T3, C6 cells using Phospho-Histone H3-S10 Rabbit mAb (AP0002) at 1:1000 dilution. HeLa, NIH/3T3 and C6 cells were treated by nocodazole (50 ng/mL) at 37℃ for 20 hours or treated by CIP(20uL/400ul) at 37℃ for 1 hour.
Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) (AS014) at 1:10000 dilution.
Lysates/proteins: 25 μg per lane.
Blocking buffer: 3% nonfat dry milk in TBST.
Detection: ECL Basic Kit (RM00020).
Exposure time: 1s.

ABclonal:Immunofluorescence - Phospho-Histone H3-S10 Rabbit mAb (AP0002)

Confocal imaging of NIH/3T3 cells using Phospho-Histone H3-S10 Rabbit mAb (AP0002, dilution 1:100) followed by a further incubation with Cy3 Goat Anti-Rabbit IgG (H+L) (AS007, dilution 1:500) (Red). The cells were counterstained with α-Tubulin Mouse mAb (AC012, dilution 1:400) followed by incubation with ABflo® 488-conjugated Goat Anti-Mouse IgG (H+L) Ab (AS076, dilution 1:500) (Green). DAPI was used for nuclear staining (Blue). Objective: 100x.

ABclonal:Immunofluorescence - Phospho-Histone H3-S10 Rabbit mAb (AP0002)

Confocal imaging of HeLa cells using Phospho-Histone H3-S10 Rabbit mAb (AP0002, dilution 1:100) followed by a further incubation with Cy3 Goat Anti-Rabbit IgG (H+L) (AS007, dilution 1:500) (Red). The cells were counterstained with α-Tubulin Mouse mAb (AC012, dilution 1:400) followed by incubation with ABflo® 488-conjugated Goat Anti-Mouse IgG (H+L) Ab (AS076, dilution 1:500) (Green). DAPI was used for nuclear staining (Blue). Objective: 100x.

ABclonal:Immunofluorescence - Phospho-Histone H3-S10 Rabbit mAb (AP0002)

Confocal imaging of C6 cells using Phospho-Histone H3-S10 Rabbit mAb (AP0002, dilution 1:100) followed by a further incubation with Cy3 Goat Anti-Rabbit IgG (H+L) (AS007, dilution 1:500) (Red). The cells were counterstained with α-Tubulin Mouse mAb (AC012, dilution 1:400) followed by incubation with ABflo® 488-conjugated Goat Anti-Mouse IgG (H+L) Ab (AS076, dilution 1:500) (Green). DAPI was used for nuclear staining (Blue). Objective: 100x.

ABclonal:Immunohistochemistry - Phospho-Histone H3-S10 Rabbit mAb (AP0002)

Immunohistochemistry analysis of paraffin-embedded Human oophoroma using Phospho-Histone H3-S10 Rabbit mAb (AP0002) at dilution of 1:100 (40x lens). High pressure antigen retrieval performed with 0.05M Tris/EDTA Buffer (pH 8.0) prior to IHC staining.

ABclonal:Immunohistochemistry - Phospho-Histone H3-S10 Rabbit mAb (AP0002)

Immunohistochemistry analysis of paraffin-embedded Mouse kidney using Phospho-Histone H3-S10 Rabbit mAb (AP0002) at dilution of 1:100 (40x lens). High pressure antigen retrieval performed with 0.05M Tris/EDTA Buffer (pH 8.0) prior to IHC staining.

Review
ABclonal: review for Phospho-Histone H3-S10 Rabbit mAb(AP0002)

Overview

Product namePhospho-Histone H3-S10 Rabbit mAb
Catalog No.AP0002
Host speciesRabbit
Purification methodAffinity purification
IsotypeIgG
CloneNo.ARC0003
Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. This structure consists of approximately 146 bp of DNA wrapped around a nucleosome, an 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 found in the large histone gene cluster on chromosome 6p22-p21.3.
ImmunogenA synthetic phosphorylated peptide around S10 of human Histone H3 (P68431).
SequenceARKST
Gene ID
Swiss Prot
SynonymsH3/A; H3C2; H3C3; H3C4; H3C6; H3C7; H3C8; H3FA; H3C10; H3C11; H3C12; HIST1H3A; Phospho-Histone H3-S10
Calculated MW15kDa
Observed MW15kDa
ReactivityHuman, Mouse, Rat, Other (Wide Range Predicted)
Tested applicationsWBIHC-PIF/ICCIPChIPChIP-seqRIPFCFC(Intra)ELISAMeDIPNucleotide ArrayDBFACSCoIPCUT&TagmeRIPInhibition
Recommended dilution
  • WB 1:500 - 1:1000
  • IHC-P 1:50 - 1:200
  • IF/ICC 1:50 - 1:200
Storage bufferStore at -20℃. Avoid freeze / thaw cycles.
Buffer: PBS with 0.02% sodium azide, 0.05% BSA, 50% glycerol, pH7.3.
Key applicationWestern blotting    Immunohistochemistry    Immunofluorescence    
Positive samplesHeLa treated by nocodazole, NIH/3T3 treated by nocodazole, C6 treated by nocodazole
Cellular locationChromosome, Nucleus
Customer validation

(HEK293T cells)

WB(Homo sapiens)

IF(Homo sapiens, Mus musculus)

Documents

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    ABclonal:Western blot - Phospho-Histone H3-S10 Rabbit mAb (AP0002)}

    Western blot - Phospho-Histone H3-S10 Rabbit mAb (AP0002)

    Western blot analysis of lysates from HeLa, NIH/3T3, C6 cells using Phospho-Histone H3-S10 Rabbit mAb (AP0002) at 1:1000 dilution. HeLa, NIH/3T3 and C6 cells were treated by nocodazole (50 ng/mL) at 37℃ for 20 hours or treated by CIP(20uL/400ul) at 37℃ for 1 hour.
    Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) (AS014) at 1:10000 dilution.
    Lysates/proteins: 25 μg per lane.
    Blocking buffer: 3% nonfat dry milk in TBST.
    Detection: ECL Basic Kit (RM00020).
    Exposure time: 1s.
    ABclonal:Immunofluorescence - Phospho-Histone H3-S10 Rabbit mAb (AP0002)}

    Immunofluorescence - Phospho-Histone H3-S10 Rabbit mAb (AP0002)

    Confocal imaging of NIH/3T3 cells using Phospho-Histone H3-S10 Rabbit mAb (AP0002, dilution 1:100) followed by a further incubation with Cy3 Goat Anti-Rabbit IgG (H+L) (AS007, dilution 1:500) (Red). The cells were counterstained with α-Tubulin Mouse mAb (AC012, dilution 1:400) followed by incubation with ABflo® 488-conjugated Goat Anti-Mouse IgG (H+L) Ab (AS076, dilution 1:500) (Green). DAPI was used for nuclear staining (Blue). Objective: 100x.
    ABclonal:Immunofluorescence - Phospho-Histone H3-S10 Rabbit mAb (AP0002)}

    Immunofluorescence - Phospho-Histone H3-S10 Rabbit mAb (AP0002)

    Confocal imaging of HeLa cells using Phospho-Histone H3-S10 Rabbit mAb (AP0002, dilution 1:100) followed by a further incubation with Cy3 Goat Anti-Rabbit IgG (H+L) (AS007, dilution 1:500) (Red). The cells were counterstained with α-Tubulin Mouse mAb (AC012, dilution 1:400) followed by incubation with ABflo® 488-conjugated Goat Anti-Mouse IgG (H+L) Ab (AS076, dilution 1:500) (Green). DAPI was used for nuclear staining (Blue). Objective: 100x.
    ABclonal:Immunofluorescence - Phospho-Histone H3-S10 Rabbit mAb (AP0002)}

    Immunofluorescence - Phospho-Histone H3-S10 Rabbit mAb (AP0002)

    Confocal imaging of C6 cells using Phospho-Histone H3-S10 Rabbit mAb (AP0002, dilution 1:100) followed by a further incubation with Cy3 Goat Anti-Rabbit IgG (H+L) (AS007, dilution 1:500) (Red). The cells were counterstained with α-Tubulin Mouse mAb (AC012, dilution 1:400) followed by incubation with ABflo® 488-conjugated Goat Anti-Mouse IgG (H+L) Ab (AS076, dilution 1:500) (Green). DAPI was used for nuclear staining (Blue). Objective: 100x.
    ABclonal:Immunohistochemistry - Phospho-Histone H3-S10 Rabbit mAb (AP0002)}

    Immunohistochemistry - Phospho-Histone H3-S10 Rabbit mAb (AP0002)

    Immunohistochemistry analysis of paraffin-embedded Human oophoroma using Phospho-Histone H3-S10 Rabbit mAb (AP0002) at dilution of 1:100 (40x lens). High pressure antigen retrieval performed with 0.05M Tris/EDTA Buffer (pH 8.0) prior to IHC staining.
    ABclonal:Immunohistochemistry - Phospho-Histone H3-S10 Rabbit mAb (AP0002)}

    Immunohistochemistry - Phospho-Histone H3-S10 Rabbit mAb (AP0002)

    Immunohistochemistry analysis of paraffin-embedded Mouse kidney using Phospho-Histone H3-S10 Rabbit mAb (AP0002) at dilution of 1:100 (40x lens). High pressure antigen retrieval performed with 0.05M Tris/EDTA Buffer (pH 8.0) prior to IHC staining.

    * For research use only. Not for therapeutic or diagnostic purposes.

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