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Low affinity neurotrophin receptor p75NTR; Low-affinity nerve growth factor receptor; NGF receptor; CD271,p75 NGF Receptor
反应种属:
Human
应用:
来源宿主:
Rabbit
类型:
Monoclonal Antibody
对比
货号-规格 货期 价格 数量
abs130295-10uL 1-2周
¥ 260 .00
abs130295-25uL 1-2周
¥ 600 .00
abs130295-100uL 1-2周
¥ 2100 .00
abs130295-500uL 1-2周
¥ 5280 .00
abs130295-1mL 1-2周
询价
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实验结果图
WB result of p75 NGF Receptor Rabbit mAb Primary antibody: p75 NGF Receptor Rabbit mAb at 1/1000 dilution Lane 1: SW480 whole cell lysate 20 µg Lane 2: neuro-2a whole cell lysate 20 µg Secondary antibody: #abs20040 at 1/10000 dilution Predicted MW: 70 kDa Observed MW: 65 kDa Exposure time: Lane 1: 2s; Lane 2: 4s
IHC shows positive staining in paraffin-embedded human tonsil. Anti-p75 NGF Receptor antibody was used at 1/500 dilution, Secondary antibody: #abs20040. Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.
IHC shows positive staining in paraffin-embedded human prostate. Anti-p75 NGF Receptor antibody was used at 1/500 dilution, Secondary antibody: #abs20040. Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.
IHC shows positive staining in nerve plexus of paraffin-embedded human colon. Anti-p75 NGF Receptor antibody was used at 1/500 dilution, Secondary antibody: #abs20040. Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.
ICC shows cytoplasmic staining in SW480 cells. Anti-p75 NGF receptor antibody was used at 1/250 dilution and incubated overnight at 4°C. Secondary antibody: #abs20025 at 1/1000 dilution (shown in green). The cells were fixed with 4% PFA and permeabilized with 0.1% PBS-Triton X-100. Nuclei were countersained with DAPI.
p75 NGF Rabbit mAb at 1/25 dilution (2µg) immunoprecipitating p75 NGF in 0.4mg SW480 whole cell lysate. Western blot was performed on the immunoprecipitate using p75 NGF Rabbit mAb at 1/1000 dilution. Secondary antibody (HRP) for IP was used at 1/400 dilution. Lane 1: SW480 whole cell lysate 10µg (input) Lane 2: p75 NGF Rabbit mAb IP in SW480 whole cell lysate Lane 3: Rabbit monoclonal IgG IP in SW480 whole cell lysate Predicted MW: 65 kDa Observed MW: 70 kDa Exposure time: 12s
Flow cytometric analysis of SW480 cells labelling p75 NGF Receptor antibody at 1/500(0.1ug) dilution/ (red) compared with a Rabbit monoclonal IgG (Black) isotype control and an unlabelled control (cells without incubation with primary antibody and secondary antibody) (Blue). Secondary antibody:#abs20025.

IHC shows positive staining in paraffin-embedded human tonsil.

Anti-p75 NGF Receptor antibody was used at 1/500 dilution, followed by a Goat Anti-Rabbit IgG H&L (HRP) ready to use. Counterstained with hematoxylin.

Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.

IHC shows positive staining in paraffin-embedded human prostate.

Anti-p75 NGF Receptor antibody was used at 1/500 dilution, followed by a Goat Anti-Rabbit IgG H&L (HRP) ready to use. Counterstained with hematoxylin.

Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.

IHC shows positive staining in nerve plexus of paraffin-embedded human colon.

Anti-p75 NGF Receptor antibody was used at 1/500 dilution, followed by a Goat Anti-Rabbit IgG H&L (HRP) ready to use. Counterstained with hematoxylin.

Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.

WB resuLt of p75 NGF Receptor Rabbit mAb                

Primary antibody: p75 NGF Receptor Rabbit mAb at 1/1000 dilution
Lane 1: SW480 whole cell lysate 20 µg
Lane 2: Neuro-2a whole cell lysate 20 µg

Secondary antibody: Goat Anti-Rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
Predicted MW: 70 kDa
Observed MW: 65 kDa
Exposure time: Lane 1: 2s
                      Lane 2: 4s

ICC shows cytoplasmic staining in SW480 cells.

Anti-p75 NGF receptor antibody was used at 1/250 dilution and incubated overnight at 4°C. Goat polyclonal Antibody to Rabbit IgG - H&L (Alexa Fluor® 488) was used as secondary antibody at 1/1000 dilution (shown in green).

The cells were fixed with 4% PFA and permeabilized with 0.1% PBS-Triton X-100. Nuclei were counterstained with DAPI.

Flow cytometric analysis of SW480 cells labelling p75 NGF Receptor antibody at 1/500(0.1ug) dilution/ (red) compared with a Rabbit monoclonal IgG (Black) isotype control and an unlabelled control (cells without incubation with primary antibody and secondary antibody) (Blue). Goat Anti-Rabbit IgG Alexa Fluor® 488 was used as the secondary antibody. 

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