Rabbit anti-α smooth muscle Actin(SMA) Recombinant Monoclonal Antibody(301-142)别名宿主反应种属应用免疫原形式浓度纯化方法类型克隆号储存/保存方法存储溶液背景说明细胞定位UniProt
概述 | |
别名 |
Alpha-actin-2; ACTA2; Smooth muscle actin; actin-sm; ASM-1; CGA7; ASM/H12
|
宿主 |
Rabbit
|
反应种属 |
Human, Mouse, Rat
|
应用 |
WB: 1:1000, IHC-P: 1:1000
|
免疫原 |
Synthetic peptide
|
性能 | |
形式 |
Liquid
|
浓度 |
0.25 mg/mL
|
纯化方法 |
Protein A affinity column
|
类型 |
Monoclonal Antibody
|
克隆号 |
301-142
|
储存/保存方法 |
Store at -20℃ for one year.
|
存储溶液 |
PBS, 40% Glycerol, 0.05% BSA, 0.03% Proclin 300
|
靶标 | |
背景说明 |
Alpha smooth muscle actin, encoded by ACTA2, is expressed in abundance in vascular smooth muscle, comprising 50–70% of total actin, with the remainder composed of β-cytoplasmic and γ-actins. Whereas α-smooth muscle expression is normally restricted to smooth muscle cells, it can also be expressed in non-muscle cells, most notably myofibroblasts that use cell traction forces to remodel extracellular matrix.
|
细胞定位 |
Cytoplasm, Cytoskeleton
|
UniProt |
P62736
|
实验结果图
WB result of SMA Rabbit mAb Primary antibody: SMA Rabbit mAb at 1/1000 dilution Lane 1: mouse lung lysate 20ug Lane 2: mouse stomach lysate 20ug Negative control: mouse lung lysate Secondary antibody: #JP20040 at 1/10000 dilution Predicted MW: 42 kDa Observed MW: 42 kDa Exposure time: 30s
IHC shows positive staining in paraffin-embedded human testis. Anti-alpha smooth muscle Actin (SMA) antibody was used at 1/1000 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-alpha smooth muscle Actin (SMA) antibody was used at 1/1000 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 hepatocellular carcinoma. Anti-alpha smooth muscle Actin (SMA) antibody was used at 1/1000 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 prostatic cancer. Anti-alpha smooth muscle Actin (SMA) antibody was used at 1/1000 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 gastric cancer. Anti-alpha smooth muscle Actin (SMA) antibody was used at 1/1000 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 mouse testis. Anti-alpha smooth muscle Actin (SMA) antibody was used at 1/1000 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 rat colon. Anti-alpha smooth muscle Actin (SMA) antibody was used at 1/1000 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 rat stomach. Anti-alpha smooth muscle Actin (SMA) antibody was used at 1/1000 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.