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TRAP1 Rabbit mAb (A25919)

Datasheet

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

ABclonal:Western blot - TRAP1 Rabbit mAb (A25919)

Western blot analysis of various lysates using TRAP1 Rabbit mAb (A25919) at 1:2000 dilution incubated overnight at 4℃.
Secondary antibody: HRP-conjugated 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: 20s.

ABclonal:Immunohistochemistry - TRAP1 Rabbit mAb (A25919)

Immunohistochemistry analysis of paraffin-embedded Human tonsil tissue using TRAP1 Rabbit mAb (A25919) at a dilution of 1:300 (40x lens). High pressure antigen retrieval performed with 0.01M Citrate Bufferr (pH 6.0) prior to IHC staining.

ABclonal:Immunohistochemistry - TRAP1 Rabbit mAb (A25919)

Immunohistochemistry analysis of paraffin-embedded Human colon carcinoma tissue using TRAP1 Rabbit mAb (A25919) at a dilution of 1:300 (40x lens). High pressure antigen retrieval performed with 0.01M Citrate Bufferr (pH 6.0) prior to IHC staining.

ABclonal:Immunohistochemistry - TRAP1 Rabbit mAb (A25919)

Immunohistochemistry analysis of paraffin-embedded Human colon tissue using TRAP1 Rabbit mAb (A25919) at a dilution of 1:300 (40x lens). High pressure antigen retrieval performed with 0.01M Citrate Bufferr (pH 6.0) prior to IHC staining.

ABclonal:Immunofluorescence - TRAP1 Rabbit mAb (A25919)

Confocal imaging of HCT 116 cells using TRAP1 Rabbit mAb (A25919, dilution 1:200) 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 - TRAP1 Rabbit mAb (A25919)

Confocal imaging of paraffin-embedded Mouse kidney tissue using TRAP1 Rabbit mAb (A25919, 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:Immunoprecipitation - TRAP1 Rabbit mAb (A25919)

Immunoprecipitation of TRAP1 from 500 µg extracts of HeLa cells was performed using 2 µg of TRAP1 Rabbit mAb (A25919). Rabbit IgG isotype control (AC042) was used to precipitate the Control IgG sample. IP samples were eluted with 1X non-reducing Laemmli Buffer. The Input lane represents 10% of the total input. Western blot analysis of immunoprecipitates was conducted using TRAP1 Rabbit mAb (A25919) at a dilution of 1:2000.

Overview

Product nameTRAP1 Rabbit mAb
Catalog No.A25919
Host speciesRabbit
Purification methodAffinity purification
IsotypeIgG
CloneNo.ARC67266
This gene encodes a mitochondrial chaperone protein that is member of the heat shock protein 90 (HSP90) family. The encoded protein has ATPase activity and interacts with tumor necrosis factor type I. This protein may function in regulating cellular stress responses. Alternate splicing results in multiple transcript variants.
ImmunogenRecombinant fusion protein containing a sequence corresponding to amino acids 445-704 of human TRAP1 (NP_057376.2).
SequenceGLFMREGIVTATEQEVKEDIAKLLRYESSALPSGQLTSLSEYASRMRAGTRNIYYLCAPNRHLAEHSPYYEAMKKKDTEVLFCFEQFDELTLLHLREFDKKKLISVETDIVVDHYKEEKFEDRSPAAECLSEKETEELMAWMRNVLGSRVTNVKVTLRLDTHPAMVTVLEMGAARHFLRMQQLAKTQEERAQLLQPTLEINPRHALIKKLNQLRASEPGLAQLLVDQIYENAMIAAGLVDDPRAMVGRLNELLVKALERH
Gene ID
Swiss Prot
SynonymsHSP75; HSP 75; HSP90L; TRAP-1
Calculated MW80kDa
Observed MW80kDa
ReactivityHuman, Mouse
Tested applicationsWBIHC-PIF/ICCIPChIPChIP-seqRIPFCFC(Intra)ELISAMeDIPNucleotide ArrayDBFACSCoIPCUT&TagmeRIPInhibition
Recommended dilution
  • WB 1:2000 - 1:8000
  • IHC-P 1:200 - 1:800
  • IF/ICC 1:200 - 1:800
  • IP 0.5μg-4μg antibody for 400μg-600μg 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 0.09% Sodium azide, 0.05% BSA, 50% glycerol, pH7.3.
Key applicationWestern blotting    Immunohistochemistry    Immunofluorescence    Immunoprecipitation    
Positive samplesHeLa, HCT 116
Cellular locationMitochondrion, Mitochondrion inner membrane, Mitochondrion matrix.

Documents

Certificate of Compliance

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ABclonal:Western blot - TRAP1 Rabbit mAb (A25919)}

Western blot - TRAP1 Rabbit mAb (A25919)

Western blot analysis of various lysates using TRAP1 Rabbit mAb (A25919) at 1:2000 dilution incubated overnight at 4℃.
Secondary antibody: HRP-conjugated 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: 20s.
ABclonal:Immunohistochemistry - TRAP1 Rabbit mAb (A25919)}

Immunohistochemistry - TRAP1 Rabbit mAb (A25919)

Immunohistochemistry analysis of paraffin-embedded Human tonsil tissue using TRAP1 Rabbit mAb (A25919) at a dilution of 1:300 (40x lens). High pressure antigen retrieval performed with 0.01M Citrate Bufferr (pH 6.0) prior to IHC staining.
ABclonal:Immunohistochemistry - TRAP1 Rabbit mAb (A25919)}

Immunohistochemistry - TRAP1 Rabbit mAb (A25919)

Immunohistochemistry analysis of paraffin-embedded Human colon carcinoma tissue using TRAP1 Rabbit mAb (A25919) at a dilution of 1:300 (40x lens). High pressure antigen retrieval performed with 0.01M Citrate Bufferr (pH 6.0) prior to IHC staining.
ABclonal:Immunohistochemistry - TRAP1 Rabbit mAb (A25919)}

Immunohistochemistry - TRAP1 Rabbit mAb (A25919)

Immunohistochemistry analysis of paraffin-embedded Human colon tissue using TRAP1 Rabbit mAb (A25919) at a dilution of 1:300 (40x lens). High pressure antigen retrieval performed with 0.01M Citrate Bufferr (pH 6.0) prior to IHC staining.
ABclonal:Immunofluorescence - TRAP1 Rabbit mAb (A25919)}

Immunofluorescence - TRAP1 Rabbit mAb (A25919)

Confocal imaging of HCT 116 cells using TRAP1 Rabbit mAb (A25919, dilution 1:200) 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 - TRAP1 Rabbit mAb (A25919)}

Immunofluorescence - TRAP1 Rabbit mAb (A25919)

Confocal imaging of paraffin-embedded Mouse kidney tissue using TRAP1 Rabbit mAb (A25919, 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:Immunoprecipitation - TRAP1 Rabbit mAb (A25919)}

Immunoprecipitation - TRAP1 Rabbit mAb (A25919)

Immunoprecipitation of TRAP1 from 500 µg extracts of HeLa cells was performed using 2 µg of TRAP1 Rabbit mAb (A25919). Rabbit IgG isotype control (AC042) was used to precipitate the Control IgG sample. IP samples were eluted with 1X non-reducing Laemmli Buffer. The Input lane represents 10% of the total input. Western blot analysis of immunoprecipitates was conducted using TRAP1 Rabbit mAb (A25919) at a dilution of 1:2000.

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

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