GLUT4 Recombinant Rabbit mAb (S-584-50)
Glut4,SLC2A4,GLUT4,Solute carrier family 2, facilitated glucose transporter member 4,Glucose transporter type 4, insulin-responsive,GLUT-4,Solute carrier family 2 facilitated glucose transporter member 4,Glucose transporter type 4 insulin-responsive (GLUT-4)
货号： S0B0602
- 价格： ￥600
- 规格：
- 数量：
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宿主来源
Rabbit分子别名
Solute carrier family 2 facilitated glucose transporter member 4, Glucose transporter type 4 insulin-responsive (GLUT-4), SLC2A4免疫原
Synthetic Peptide细胞定位
Cell membrane, CytoplasmAccession
P14672克隆号
S-584-50抗体类型
Recombinant mAb抗体同种型
IgG应用
IHC-P, WB, IP反应种属 ?
Hu, Ms, Rt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 | 1:1000 |
| IP | 1:50 |
| IHC-P | 1:500-1:2000 |
GLUT4 is the insulin-regulated glucose transporter found primarily in adipose tissues and striated muscle (skeletal and cardiac). At the cell surface, GLUT4 permits the facilitated diffusion of circulating glucose down its concentration gradient into muscle and fat cells. Once within cells, glucose is rapidly phosphorylated by glucokinase in the liver and hexokinase in other tissues to form glucose-6-phosphate, which then enters glycolysis or is polymerized into glycogen. In addition, recent reports demonstrated the presence of GLUT4 gene in central nervous system such as the hippocampus. Moreover, impairment in insulin-stimulated trafficking of GLUT4 in the hippocampus result in decreased metabolic activities and plasticity of hippocampal neurons, which leads to depressive like behaviour and cognitive dysfunction.
免疫印迹
WB result of GLUT4 Rabbit mAb
Primary antibody: GLUT4 Rabbit mAb at 1/1000 dilution
Lane 1: unboiled mouse heart lysate 20 µg
Lane 2: unboiled mouse skeletal muscle lysate 20 µg
Secondary antibody: Goat Anti-rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
Predicted MW: 55 kDa
Observed MW: 40~55 kDaWB result of GLUT4 Rabbit mAb
Primary antibody: GLUT4 Rabbit mAb at 1/1000 dilution
Lane 1: unboiled rat heart lysate 20 µg
Lane 2: unboiled rat skeletal muscle lysate 20 µg
Secondary antibody: Goat Anti-rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
Predicted MW: 55 kDa
Observed MW: 40~55 kDa
免疫沉淀
GLUT4 Rabbit mAb at 1/50 dilution (1 µg) immunoprecipitating GLUT4 in 0.4 mg mouse heart lysate.
Western blot was performed on the immunoprecipitate using GLUT4 Rabbit mAb at 1/1000 dilution.
Secondary antibody (HRP) for IP was used at 1/400 dilution.
Lane 1: mouse heart lysate 20 µg (Input)
Lane 2: GLUT4 Rabbit mAb IP in mouse heart lysate
Lane 3: Rabbit monoclonal IgG IP in mouse heart lysate
Predicted MW: 55 kDa
Observed MW: 40~55 kDa
免疫组化
IHC shows positive staining in paraffin-embedded human cardiac muscle. Anti-GLUT4 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 skeletal muscle. Anti-GLUT4 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 liver. Anti-GLUT4 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 mouse cardiac muscle. Anti-GLUT4 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 mouse skeletal muscle. Anti-GLUT4 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 rat cardiac muscle. Anti-GLUT4 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.
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