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Rabbit抗原名称
PGP9.5分子别名
Ubiquitin carboxyl-terminal hydrolase isozyme L1, UCH-L1, Neuron cytoplasmic protein 9.5, Ubiquitin thioesterase L1免疫原
Synthetic Peptide细胞定位
CytoplasmAccession
P09936克隆号
SDT-665-37抗体类型
Recombinant mAb抗体同种型
IgG应用
ICFCM, IHC-P, ICC, WB反应种属 ?
Hu, Ms, Rt预测反应种属
(反应种属缩写表)Mq, Pg, Hr, Dg纯化方式
Protein A浓度
0.5 mg/ml标记
Unconjugated性状
Liquid缓冲体系
PBS, 40% Glycerol, 0.05% BSA, 0.03% Proclin 300储存条件
12 months from date of receipt / reconstitution, -20 °C as supplied
应用 | 稀释度 |
---|---|
WB | 1:2000 |
IHC-P | 1:500-1:2000 |
ICC | 1:500 |
ICFCM | 1:5000 |
Protein gene product 9.5 (PGP 9.5), also known as ubiquitin carboxyl-terminal hydrolase-1 (UCH-L1), is a 25 kDa protein originally isolated from whole brain extracts. In non-neoplastic tissues, PGP 9.5, a member of the ubiquitin hydrolase family of proteins, is confined to neural and neuroendocrine cells. In the field of diagnostic surgical pathology, PGP9.5 is used as a purportedly specific marker of putative neural and neuroectodermal tumors.
免疫印迹
WB result of PGP9.5 Rabbit mAb
Primary antibody: PGP9.5 Rabbit mAb at 1/2000 dilution
Lane 1: LNCaP whole cell lysate 5 µg
Lane 2: DU 145 whole cell lysate 5 µg
Lane 3: SH-SY5Y whole cell lysate 5 µg
Lane 4: Ramos whole cell lysate 5 µg
Lane 5: HEK-293 whole cell lysate 5 µg
Negative control: LNCaP whole cell lysate
Secondary antibody: Goat Anti-rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
Predicted MW: 25 kDa
Observed MW: 23 kDa
WB result of PGP9.5 Rabbit mAb
Primary antibody: PGP9.5 Rabbit mAb at 1/2000 dilution
Lane 1: mouse brain lysate 5 µg
Secondary antibody: Goat Anti-rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
Predicted MW: 25 kDa
Observed MW: 23 kDaWB result of PGP9.5 Rabbit mAb
Primary antibody: PGP9.5 Rabbit mAb at 1/2000 dilution
Lane 1: rat brain lysate 5 µg
Secondary antibody: Goat Anti-rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
Predicted MW: 25 kDa
Observed MW: 23 kDa
流式分析
Flow cytometric analysis of 4% PFA fixed 90% methanol permeabilized Hela (Human cervix adenocarcinoma epithelial cell, left) / SH-SY5Y (Human neuroblastoma epithelial cell, Right) labelling PGP9.5 antibody at 1/5000 dilution (0.01 μg) / (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. Negative control: Hela
免疫组化
IHC shows positive staining in paraffin-embedded human cerebral cortex. Anti-PGP9.5 antibody was used at 1/2000 dilution, followed by a HRP Polymer for Mouse & Rabbit IgG (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 cerebellum. Anti-PGP9.5 antibody was used at 1/500 dilution, followed by a HRP Polymer for Mouse & Rabbit IgG (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 colon. Anti-PGP9.5 antibody was used at 1/500 dilution, followed by a HRP Polymer for Mouse & Rabbit IgG (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 kidney. Anti-PGP9.5 antibody was used at 1/2000 dilution, followed by a HRP Polymer for Mouse & Rabbit IgG (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 pancreas. Anti-PGP9.5 antibody was used at 1/2000 dilution, followed by a HRP Polymer for Mouse & Rabbit IgG (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 ovarian cancer. Anti-PGP9.5 antibody was used at 1/500 dilution, followed by a HRP Polymer for Mouse & Rabbit IgG (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 pancreatic cancer. Anti-PGP9.5 antibody was used at 1/500 dilution, followed by a HRP Polymer for Mouse & Rabbit IgG (ready to use). 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 human invasive ductal breast cancer. Anti-PGP9.5 antibody was used at 1/2000 dilution, followed by a HRP Polymer for Mouse & Rabbit IgG (ready to use). Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.
免疫细胞化学
ICC shows positive staining in SH-SY5Y cells (top panel) and negative staining in HeLa cells (below panel). Anti-PGP9.5 antibody was used at 1/500 dilution (Green) 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. The cells were fixed with 100% ice-cold methanol and permeabilized with 0.1% PBS-Triton X-100. Nuclei were counterstained with DAPI (Blue). Counterstain with tubulin (Red).
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