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pan Phospho-Serine/Threonine Mouse mAb (AP1067)

Publications (4) Datasheet

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

ABclonal:Western blot - pan Phospho-Serine/Threonine Mouse mAb (AP1067)

Western blot analysis of lysates from A-431 cells using pan Phospho-Serine/Threonine Mouse mAb (AP1067) at 1:1000 dilution incubated overnight at 4℃. A-431 cells were treated by Calyculin A (50 nM) at 37℃ for 30 minutes after serum-starvation overnight.
Secondary antibody: HRP-conjugated Goat anti-Mouse IgG (H+L) (AS003) 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: 60s.

ABclonal:Immunohistochemistry - pan Phospho-Serine/Threonine Mouse mAb (AP1067)

Immunohistochemistry analysis of paraffin-embedded Rat liver tissue, untreated (left) and lambda phosphatase-treated (right), using pan Phospho-Serine/Threonine Mouse mAb (AP1067) at a dilution of 1:2000 (40x lens). High pressure antigen retrieval performed with 0.01M Citrate Buffer (pH 6.0) prior to IHC staining.

ABclonal:Immunohistochemistry - pan Phospho-Serine/Threonine Mouse mAb (AP1067)

Immunohistochemistry analysis of paraffin-embedded Mouse liver tissue, untreated (left) and lambda phosphatase-treated (right), using pan Phospho-Serine/Threonine Mouse mAb (AP1067) at a dilution of 1:2000 (40x lens). High pressure antigen retrieval performed with 0.01M Citrate Buffer (pH 6.0) prior to IHC staining.

ABclonal:Immunohistochemistry - pan Phospho-Serine/Threonine Mouse mAb (AP1067)

Immunohistochemistry analysis of paraffin-embedded Human lung cancer tissue, untreated (left) and lambda phosphatase-treated (right), using pan Phospho-Serine/Threonine Mouse mAb (AP1067) at a dilution of 1:2000 (40x lens). High pressure antigen retrieval performed with 0.01M Citrate Buffer (pH 6.0) prior to IHC staining.

Overview

Product namepan Phospho-Serine/Threonine Mouse mAb
Catalog No.AP1067
Host speciesMouse
Purification methodAffinity purification
IsotypeIgG2b, kappa
CloneNo.AMC0265
Protein phosphorylation is one of the main key regulatory mechanisms by which extracellular signals are conveyed. Global alteration of signal transduction by inhibition of serine/threonine dephosphorylation has recently been shown to markedly potentiate cancer cell killing by the DNA-methylating drug, temozolomide.
ImmunogenA synthetic peptide corresponding to a sequence containing phosphorylated Serine/Threonine.
SequenceEmail for sequence
Gene ID
Swiss Prot
Synonyms
Calculated MW
Observed MW>10kDa
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 1:1000 - 1:5000
Storage bufferStore at -20℃. Avoid freeze / thaw cycles.
Buffer: PBS with 0.09% Sodium azide, 50% glycerol, pH7.3.
Key applicationWestern blotting    Immunohistochemistry    
Positive samplesA-431 treated by Calyculin A
Cellular location
Customer validation

WB(Mus musculus, Other, Homo sapiens)

IF(Mus musculus)

IHC(Mus musculus)

RT-qPCR(Mus musculus)

WB(Mus musculus)

Documents

Certificate of Compliance

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Lot number

    ABclonal:Western blot - pan Phospho-Serine/Threonine Mouse mAb (AP1067)}

    Western blot - pan Phospho-Serine/Threonine Mouse mAb (AP1067)

    Western blot analysis of lysates from A-431 cells using pan Phospho-Serine/Threonine Mouse mAb (AP1067) at 1:1000 dilution incubated overnight at 4℃. A-431 cells were treated by Calyculin A (50 nM) at 37℃ for 30 minutes after serum-starvation overnight.
    Secondary antibody: HRP-conjugated Goat anti-Mouse IgG (H+L) (AS003) 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: 60s.
    ABclonal:Immunohistochemistry - pan Phospho-Serine/Threonine Mouse mAb (AP1067)}

    Immunohistochemistry - pan Phospho-Serine/Threonine Mouse mAb (AP1067)

    Immunohistochemistry analysis of paraffin-embedded Rat liver tissue, untreated (left) and lambda phosphatase-treated (right), using pan Phospho-Serine/Threonine Mouse mAb (AP1067) at a dilution of 1:2000 (40x lens). High pressure antigen retrieval performed with 0.01M Citrate Buffer (pH 6.0) prior to IHC staining.
    ABclonal:Immunohistochemistry - pan Phospho-Serine/Threonine Mouse mAb (AP1067)}

    Immunohistochemistry - pan Phospho-Serine/Threonine Mouse mAb (AP1067)

    Immunohistochemistry analysis of paraffin-embedded Mouse liver tissue, untreated (left) and lambda phosphatase-treated (right), using pan Phospho-Serine/Threonine Mouse mAb (AP1067) at a dilution of 1:2000 (40x lens). High pressure antigen retrieval performed with 0.01M Citrate Buffer (pH 6.0) prior to IHC staining.
    ABclonal:Immunohistochemistry - pan Phospho-Serine/Threonine Mouse mAb (AP1067)}

    Immunohistochemistry - pan Phospho-Serine/Threonine Mouse mAb (AP1067)

    Immunohistochemistry analysis of paraffin-embedded Human lung cancer tissue, untreated (left) and lambda phosphatase-treated (right), using pan Phospho-Serine/Threonine Mouse mAb (AP1067) at a dilution of 1:2000 (40x lens). High pressure antigen retrieval performed with 0.01M Citrate Buffer (pH 6.0) prior to IHC staining.

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

    Publishing research using AP1067? Please let us know so that we can cite the reference in this datasheet.

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    Secondary Antibodies (22)