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PU.1/SPI1 Rabbit mAb (A24910)

Publication (1) Datasheet

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

ABclonal:Western blot - PU.1/SPI1 Rabbit mAb (A24910)

Western blot analysis of various lysates, using PU.1/SPI1 Rabbit mAb (A24910) at 1:1000 dilution.
Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) (AS014) at 1:10000 dilution.
Lysates/proteins: 25μg per lane.
Blocking buffer: 3% nonfat dry milk in TBST.
Detection: ECL Basic Kit (RM00020).
Negative control (NC):HAP1
Exposure time: 15s.

ABclonal:Immunohistochemistry - PU.1/SPI1 Rabbit mAb (A24910)

Immunohistochemistry analysis of paraffin-embedded Human appendix tissue using PU.1/SPI1 Rabbit mAb (A24910) at a dilution of 1:3000 (40x lens). High pressure antigen retrieval performed with 0.01M Tris-EDTA Buffer (pH 9.0) prior to IHC staining.

ABclonal:Immunohistochemistry - PU.1/SPI1 Rabbit mAb (A24910)

Immunohistochemistry analysis of paraffin-embedded Human follicular lymphoma tissue using PU.1/SPI1 Rabbit mAb (A24910) at a dilution of 1:3000 (40x lens). High pressure antigen retrieval performed with 0.01M Tris-EDTA Buffer (pH 9.0) prior to IHC staining.

ABclonal:Immunohistochemistry - PU.1/SPI1 Rabbit mAb (A24910)

Immunohistochemistry analysis of paraffin-embedded Human tonsil tissue using PU.1/SPI1 Rabbit mAb (A24910) at a dilution of 1:3000 (40x lens). High pressure antigen retrieval performed with 0.01M Tris-EDTA Buffer (pH 9.0) prior to IHC staining.

ABclonal:Immunofluorescence - PU.1/SPI1 Rabbit mAb (A24910)

Confocal imaging of THP-1 cells using PU.1/SPI1 Rabbit mAb (A24910, dilution 1:200) 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 - PU.1/SPI1 Rabbit mAb (A24910)

Confocal imaging of paraffin-embedded Human spleen tissue using PU.1/SPI1 Rabbit mAb (A24910, dilution 1:200) 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). High pressure antigen retrieval performed with 0.01M Citrate Buffer (pH 6.0) prior to IF staining. Objective: 40x.

ABclonal:Flow CytoMetry - PU.1/SPI1 Rabbit mAb (A24910)

Flow cytometry: 1X10^6 HAP1 cells (negative control, left) and THP-1 cells (right) were intracellularly-stained with PU.1/SPI1 Rabbit mAb (A24910, 2 μg/mL, orange line) or ABflo® 594 Rabbit IgG isotype control (A23821, 5 μl/Test, blue line), followed by ABflo® 594-conjugated Goat Anti-Rabbit IgG (H+L) staining. Non-fluorescently stained cells were used as blank control (red line).

ABclonal:Flow CytoMetry - PU.1/SPI1 Rabbit mAb (A24910)

Flow cytometry: 1X10^6 THP-1 cells were intracellularly-stained with ABflo® 594 Rabbit IgG isotype control (A23821, 5 μl/Test, left) or PU.1/SPI1 Rabbit mAb (A24910, 2 μg/mL, right).

Overview

Product namePU.1/SPI1 Rabbit mAb
Catalog No.A24910
Host speciesRabbit
Purification methodAffinity purification
IsotypeIgG
CloneNo.ARC63111
This gene encodes an ETS-domain transcription factor that activates gene expression during myeloid and B-lymphoid cell development. The nuclear protein binds to a purine-rich sequence known as the PU-box found near the promoters of target genes, and regulates their expression in coordination with other transcription factors and cofactors. The protein can also regulate alternative splicing of target genes. Multiple transcript variants encoding different isoforms have been found for this gene.
ImmunogenA synthetic peptide corresponding to a sequence within amino acids 1-100 of human PU.1/SPI1 (NP_003111.2)
SequenceMLQACKMEGFPLVPPPSEDLVPYDTDLYQRQTHEYYPYLSSDGESHSDHYWDFHPHHVHSEFESFAENNFTELQSVQPPQLQQLYRHMELEQMHVLDTPM
Gene ID
Swiss Prot
SynonymsOF; PU.1; AGM10; SFPI1; SPI-1; SPI-A; PU.1/SPI1
Calculated MW31kDa
Observed MW38kDa
ReactivityHuman, Rat
Tested applicationsWBIHC-PIF/ICCIPChIPChIP-seqRIPFCFC(Intra)ELISAMeDIPNucleotide ArrayDBFACSCoIPCUT&TagmeRIPInhibition
Recommended dilution
  • WB 1:500 - 1:1000
  • IHC-P 1:500 - 1:5000
  • IF/ICC 1:50 - 1:200
  • FC (intra) 1:100 - 1:500
  • ELISA Recommended starting concentration is 1 μg/mL. Please optimize the concentration based on your specific assay requirements.
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    Immunohistochemistry    Immunofluorescence    
Positive samplesDaudi
Cellular locationnucleoplasm, nucleus.
Customer validation

WB(Homo sapiens)

Documents

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ABclonal:Western blot - PU.1/SPI1 Rabbit mAb (A24910)}

Western blot - PU.1/SPI1 Rabbit mAb (A24910)

Western blot analysis of various lysates, using PU.1/SPI1 Rabbit mAb (A24910) at 1:1000 dilution.
Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) (AS014) at 1:10000 dilution.
Lysates/proteins: 25μg per lane.
Blocking buffer: 3% nonfat dry milk in TBST.
Detection: ECL Basic Kit (RM00020).
Negative control (NC):HAP1
Exposure time: 15s.
ABclonal:Immunohistochemistry - PU.1/SPI1 Rabbit mAb (A24910)}

Immunohistochemistry - PU.1/SPI1 Rabbit mAb (A24910)

Immunohistochemistry analysis of paraffin-embedded Human appendix tissue using PU.1/SPI1 Rabbit mAb (A24910) at a dilution of 1:3000 (40x lens). High pressure antigen retrieval performed with 0.01M Tris-EDTA Buffer (pH 9.0) prior to IHC staining.
ABclonal:Immunohistochemistry - PU.1/SPI1 Rabbit mAb (A24910)}

Immunohistochemistry - PU.1/SPI1 Rabbit mAb (A24910)

Immunohistochemistry analysis of paraffin-embedded Human follicular lymphoma tissue using PU.1/SPI1 Rabbit mAb (A24910) at a dilution of 1:3000 (40x lens). High pressure antigen retrieval performed with 0.01M Tris-EDTA Buffer (pH 9.0) prior to IHC staining.
ABclonal:Immunohistochemistry - PU.1/SPI1 Rabbit mAb (A24910)}

Immunohistochemistry - PU.1/SPI1 Rabbit mAb (A24910)

Immunohistochemistry analysis of paraffin-embedded Human tonsil tissue using PU.1/SPI1 Rabbit mAb (A24910) at a dilution of 1:3000 (40x lens). High pressure antigen retrieval performed with 0.01M Tris-EDTA Buffer (pH 9.0) prior to IHC staining.
ABclonal:Immunofluorescence - PU.1/SPI1 Rabbit mAb (A24910)}

Immunofluorescence - PU.1/SPI1 Rabbit mAb (A24910)

Confocal imaging of THP-1 cells using PU.1/SPI1 Rabbit mAb (A24910, dilution 1:200) 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 - PU.1/SPI1 Rabbit mAb (A24910)}

Immunofluorescence - PU.1/SPI1 Rabbit mAb (A24910)

Confocal imaging of paraffin-embedded Human spleen tissue using PU.1/SPI1 Rabbit mAb (A24910, dilution 1:200) 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). High pressure antigen retrieval performed with 0.01M Citrate Buffer (pH 6.0) prior to IF staining. Objective: 40x.
ABclonal:Flow CytoMetry - PU.1/SPI1 Rabbit mAb (A24910)}

Flow CytoMetry - PU.1/SPI1 Rabbit mAb (A24910)

Flow cytometry: 1X10^6 HAP1 cells (negative control, left) and THP-1 cells (right) were intracellularly-stained with PU.1/SPI1 Rabbit mAb (A24910, 2 μg/mL, orange line) or ABflo® 594 Rabbit IgG isotype control (A23821, 5 μl/Test, blue line), followed by ABflo® 594-conjugated Goat Anti-Rabbit IgG (H+L) staining. Non-fluorescently stained cells were used as blank control (red line).
ABclonal:Flow CytoMetry - PU.1/SPI1 Rabbit mAb (A24910)}

Flow CytoMetry - PU.1/SPI1 Rabbit mAb (A24910)

Flow cytometry: 1X10^6 THP-1 cells were intracellularly-stained with ABflo® 594 Rabbit IgG isotype control (A23821, 5 μl/Test, left) or PU.1/SPI1 Rabbit mAb (A24910, 2 μg/mL, right).

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

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항체 (5)

Secondary Antibodies (26)