4 专属买赠 2 满额赠礼
Lyt-2,CD8 alpha
反应种属:
Mouse
应用:
来源宿主:
Rabbit
类型:
Monoclonal Antibody
对比
货号-规格 货期 价格 数量
abs171703-25uL 1-2周
¥ 600 .00
abs171703-100uL 1-2周
¥ 2100 .00
abs171703-1mL 1-2周
询价
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实验结果图
WB result of CD8α Rabbit mAb Primary antibody: CD8α Rabbit mAb at 1/1000 dilution Lane 1: RAW 264.7 whole cell lysate 20 µg Lane 2: mouse thymus lysate 20 µg Negative control: RAW 264.7 whole cell lysate Secondary antibody: #abs20040 at 1/10000 dilution Predicted MW: 29 kDa Observed MW: 28~37 kDa Exposure time: 60s
IHC shows positive staining in paraffin-embedded mouse thymus. Anti-CD8α 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 mouse spleen. Anti-CD8α 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 mouse colon. Anti-CD8α 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.
Negative control: IHC shows negative staining in paraffin-embedded mouse cardiac muscle. Anti-CD8α 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 positive staining in paraffin-embedded mouse thymus. Anti-CD8α antibody was used at 1/1000 dilution and incubated overnight at 4°C. Secondary antibody: #abs20025 at 1/1000 dilution.Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with ICC staining protocol. Nuclei were counterstained with DAPI.
Flow cytometric analysis of mouse primary splenocytes labeling CD8α antibody at 1/50 (1 μg) dilution / (right panel) compared with a Rabbit IgG, Isotype Control / (left panel). Secondary antibody: #abs20025 was used as the secondary antibody. Cells were surface stained with CD4-Alexa Fluor® 647, then stained with rabbit IgG (Left) / CD8α (Right) separately. CD4 and CD8α are mutually exclusive expressed in mouse spleen. Gated on total viable cells.
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