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EGR1 Rabbit mAb (A23424)

Datasheet

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

ABclonal:Western blot - EGR1 Rabbit mAb (A23424)

Western blot analysis of lysates from 293T cells, using EGR1 Rabbit mAb (A23424) at 1:1000 dilution. 293T cells were treated by 20% FBS at 37℃ for 2 hours after serum-starvation overnight.
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).
Exposure time: 5s.

ABclonal:Western blot - EGR1 Rabbit mAb (A23424)

Western blot analysis of lysates from C2C12 cells, using EGR1 Rabbit mAb (A23424) at 1:1000 dilution. C2C12 cells were treated by EGF (100 ng/ml) at 37℃ for 30 minutes after serum-starvation overnight.
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).
Exposure time: 5s.

ABclonal:Immunohistochemistry - EGR1 Rabbit mAb (A23424)

Immunohistochemistry analysis of paraffin-embedded Human thyroid cancer tissue using EGR1 Rabbit mAb (A23424) at a dilution of 1:200 (40x lens). High pressure antigen retrieval performed with 0.01M Citrate Bufferr (pH 6.0) prior to IHC staining.

ABclonal:Immunofluorescence - EGR1 Rabbit mAb (A23424)

Confocal imaging of paraffin-embedded Mouse brain tissue using EGR1 Rabbit mAb (A23424, 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). Microwave antigen retrieval performed with 0.01M Citrate Buffer (pH 6.0) prior to IF staining. Objective: 40x.

ABclonal:Immunofluorescence - EGR1 Rabbit mAb (A23424)

Confocal imaging of paraffin-embedded Rat brain tissue using EGR1 Rabbit mAb (A23424, 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). Microwave antigen retrieval performed with 0.01M Citrate Buffer (pH 6.0) prior to IF staining. Objective: 40x.

Overview

Product nameEGR1 Rabbit mAb
Catalog No.A23424
Host speciesRabbit
Purification methodAffinity purification
IsotypeIgG
CloneNo.ARC60244
The protein encoded by this gene belongs to the EGR family of C2H2-type zinc-finger proteins. It is a nuclear protein and functions as a transcriptional regulator. The products of target genes it activates are required for differentitation and mitogenesis. Studies suggest this is a cancer suppressor gene.
ImmunogenRecombinant fusion protein containing a sequence corresponding to amino acids 90-250aa of human EGR1(NP_001955.1).
SequenceADTGEQPYEHLTAESFPDISLNNEKVLVETSYPSQTTRLPPITYTGRFSLEPAPNSGNTLWPEPLFSLVSGLVSMTNPPASSSSAPSPAASSASASQSPPLSCAVPSNDSSPIYSAAPTFPTPNTDIFPEPQSQAFPGSAGTALQYPPPAYPAAKGGFQVP
Gene ID
Swiss Prot
SynonymsTIS8; AT225; G0S30; NGFI-A; ZNF225; KROX-24; ZIF-268; EGR1
Calculated MW58kDa
Observed MW75-80kDa
ReactivityHuman, Mouse, Rat
Tested applicationsWBIHC-PIF/ICCIPChIPChIP-seqRIPFCFC(Intra)ELISAMeDIPNucleotide ArrayDBFACSCoIPCUT&TagmeRIPInhibition
Recommended dilution
  • WB 1:1000 - 1:6000
  • IHC-P 1:200-1:800
  • IF/ICC 1:200 - 1:800
  • IP 0.5μg-4μg antibody for 200μg-400μg extracts of whole cells
  • 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 0.05% proclin300, 0.05% BSA, 50% glycerol, pH7.3.
Key applicationWestern blotting    Immunofluorescence    Immunoprecipitation    
Positive samples293T treated by FBS, C2C12 treated by EGF
Cellular locationNucleus.
Customer validation

Other(Homo sapiens)

Documents

Certificate of Compliance

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ABclonal:Western blot - EGR1 Rabbit mAb (A23424)}

Western blot - EGR1 Rabbit mAb (A23424)

Western blot analysis of lysates from 293T cells, using EGR1 Rabbit mAb (A23424) at 1:1000 dilution. 293T cells were treated by 20% FBS at 37℃ for 2 hours after serum-starvation overnight.
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).
Exposure time: 5s.
ABclonal:Western blot - EGR1 Rabbit mAb (A23424)}

Western blot - EGR1 Rabbit mAb (A23424)

Western blot analysis of lysates from C2C12 cells, using EGR1 Rabbit mAb (A23424) at 1:1000 dilution. C2C12 cells were treated by EGF (100 ng/ml) at 37℃ for 30 minutes after serum-starvation overnight.
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).
Exposure time: 5s.
ABclonal:Immunohistochemistry - EGR1 Rabbit mAb (A23424)}

Immunohistochemistry - EGR1 Rabbit mAb (A23424)

Immunohistochemistry analysis of paraffin-embedded Human thyroid cancer tissue using EGR1 Rabbit mAb (A23424) at a dilution of 1:200 (40x lens). High pressure antigen retrieval performed with 0.01M Citrate Bufferr (pH 6.0) prior to IHC staining.
ABclonal:Immunofluorescence - EGR1 Rabbit mAb (A23424)}

Immunofluorescence - EGR1 Rabbit mAb (A23424)

Confocal imaging of paraffin-embedded Mouse brain tissue using EGR1 Rabbit mAb (A23424, 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). Microwave antigen retrieval performed with 0.01M Citrate Buffer (pH 6.0) prior to IF staining. Objective: 40x.
ABclonal:Immunofluorescence - EGR1 Rabbit mAb (A23424)}

Immunofluorescence - EGR1 Rabbit mAb (A23424)

Confocal imaging of paraffin-embedded Rat brain tissue using EGR1 Rabbit mAb (A23424, 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). Microwave antigen retrieval performed with 0.01M Citrate Buffer (pH 6.0) prior to IF staining. Objective: 40x.

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

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