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Phospho-Histone H2AX-S139 Rabbit mAb (AP1555)

Datasheet

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

ABclonal:Western blot - Phospho-Histone H2AX-S139 Rabbit mAb (AP1555)

Western blot analysis of various lysates using Phospho-Histone H2AX-S139 Rabbit mAb (AP1555) at 1:1000 dilution incubated overnight at 4℃. 293T and C6 cells were treated by UV at room temperature for 15-30 minutes.
Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) (AS014) at 1:10000 dilution.
Lysates/proteins: 30 μg per lane.
Blocking buffer: 3% nonfat dry milk in TBST.
Detection: ECL Basic Kit (RM00020).
Exposure time: 20s.

ABclonal:Western blot - Phospho-Histone H2AX-S139 Rabbit mAb (AP1555)

Western blot analysis of lysates from NIH/3T3 cells using Phospho-Histone H2AX-S139 Rabbit mAb (AP1555) at 1:1000 dilution incubated overnight at 4℃. NIH/3T3 cells were treated by UV at room temperature for 15-30 minutes.
Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) (AS014) at 1:10000 dilution.
Lysates/proteins: 30 μg per lane.
Blocking buffer: 3 % nonfat dry milk in TBST.
Detection: ECL Basic Kit (RM00020).
Exposure time: 45s.

ABclonal:Immunofluorescence - Phospho-Histone H2AX-S139 Rabbit mAb (AP1555)

Confocal imaging of 293T cells (treated with UV) and 293T cells (untreated) using Phospho-Histone H2AX-S139 Rabbit mAb (AP1555, dilution 1:2000) followed by a further incubation with Cy3 Goat Anti-Rabbit IgG (H+L) (AS007, dilution 1:500) (Red). DAPI was used for nuclear staining (Blue). Objective: 100x.

ABclonal:Immunofluorescence - Phospho-Histone H2AX-S139 Rabbit mAb (AP1555)

Confocal imaging of NIH/3T3 cells (treated with UV) and NIH/3T3 cells (untreated) using Phospho-Histone H2AX-S139 Rabbit mAb (AP1555, dilution 1:2000) 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 H2AX-S139 Rabbit mAb (AP1555)

Confocal imaging of C6 cells (treated with UV) and C6 cells (untreated) using Phospho-Histone H2AX-S139 Rabbit mAb (AP1555, dilution 1:2000) 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.

Overview

Product namePhospho-Histone H2AX-S139 Rabbit mAb
Catalog No.AP1555
Host speciesRabbit
Purification methodAffinity purification
IsotypeIgG
CloneNo.ARC70654
Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This gene encodes a replication-independent histone that is a member of the histone H2A family, and generates two transcripts through the use of the conserved stem-loop termination motif, and the polyA addition motif.
ImmunogenA synthetic phosphorylated peptide around S139 of human Histone H2AX (NP_002096.1).
SequenceQASQEY
Gene ID
Swiss Prot
SynonymsH2A.X; H2A/X; H2AFX
Calculated MW15kDa
Observed MW15-17kDa/17kDa
ReactivityHuman, Mouse, Rat
Tested applicationsWBIHC-PIF/ICCIPChIPChIP-seqRIPFCFC(Intra)ELISAMeDIPNucleotide ArrayDBFACSCoIPCUT&TagmeRIPInhibition
Recommended dilution
  • WB 1:1000 - 1:4000
  • IF/ICC 1:400-1:4000
Storage bufferStore at -20℃. Avoid freeze / thaw cycles.
Buffer: PBS with 0.09% Sodium azide, 0.05% BSA, 50% glycerol, pH7.3.
Key applicationWestern blotting    Immunofluorescence    
Positive samplesNIH/3T3, 293T, C6
Cellular locationChromosome, Nucleus.

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ABclonal:Western blot - Phospho-Histone H2AX-S139 Rabbit mAb (AP1555)}

Western blot - Phospho-Histone H2AX-S139 Rabbit mAb (AP1555)

Western blot analysis of various lysates using Phospho-Histone H2AX-S139 Rabbit mAb (AP1555) at 1:1000 dilution incubated overnight at 4℃. 293T and C6 cells were treated by UV at room temperature for 15-30 minutes.
Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) (AS014) at 1:10000 dilution.
Lysates/proteins: 30 μg per lane.
Blocking buffer: 3% nonfat dry milk in TBST.
Detection: ECL Basic Kit (RM00020).
Exposure time: 20s.
ABclonal:Western blot - Phospho-Histone H2AX-S139 Rabbit mAb (AP1555)}

Western blot - Phospho-Histone H2AX-S139 Rabbit mAb (AP1555)

Western blot analysis of lysates from NIH/3T3 cells using Phospho-Histone H2AX-S139 Rabbit mAb (AP1555) at 1:1000 dilution incubated overnight at 4℃. NIH/3T3 cells were treated by UV at room temperature for 15-30 minutes.
Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) (AS014) at 1:10000 dilution.
Lysates/proteins: 30 μg per lane.
Blocking buffer: 3 % nonfat dry milk in TBST.
Detection: ECL Basic Kit (RM00020).
Exposure time: 45s.
ABclonal:Immunofluorescence - Phospho-Histone H2AX-S139 Rabbit mAb (AP1555)}

Immunofluorescence - Phospho-Histone H2AX-S139 Rabbit mAb (AP1555)

Confocal imaging of 293T cells (treated with UV) and 293T cells (untreated) using Phospho-Histone H2AX-S139 Rabbit mAb (AP1555, dilution 1:2000) followed by a further incubation with Cy3 Goat Anti-Rabbit IgG (H+L) (AS007, dilution 1:500) (Red). DAPI was used for nuclear staining (Blue). Objective: 100x.
ABclonal:Immunofluorescence - Phospho-Histone H2AX-S139 Rabbit mAb (AP1555)}

Immunofluorescence - Phospho-Histone H2AX-S139 Rabbit mAb (AP1555)

Confocal imaging of NIH/3T3 cells (treated with UV) and NIH/3T3 cells (untreated) using Phospho-Histone H2AX-S139 Rabbit mAb (AP1555, dilution 1:2000) 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 H2AX-S139 Rabbit mAb (AP1555)}

Immunofluorescence - Phospho-Histone H2AX-S139 Rabbit mAb (AP1555)

Confocal imaging of C6 cells (treated with UV) and C6 cells (untreated) using Phospho-Histone H2AX-S139 Rabbit mAb (AP1555, dilution 1:2000) 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.

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

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