- ￥5800
- GeneTex
- 美国
- GTX60393
- 2025年07月16日
- WB, ICC/IF, FACS, ELISA
- Mouse
- Human, Mouse, Rat, Monkey
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- 详细信息
- 文献和实验
- 技术资料
- 免疫原：
Purified recombinant fragment of human ACTA2 expressed in E. Coli.
- 亚型：
IgG1
- 形态：
Liquid
- 保存条件：
Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4ºC. For long-term storage, aliquot and store at -20ºC or below. Avoid multiple freeze-thaw cycles.
- 克隆性：
Monoclonal
- 标记物：
Unconjugated
- 适应物种：
Human, Mouse, Rat, Monkey
- 保质期：
12 months from the shipping date of the product.
- 抗原来源：
Human
- 目录编号：
GTX60393
- 级别：
Primary Antibodies
- 库存：
Available
- 供应商：
GeneTex
- 宿主：
Mouse
- 应用范围：
WB, ICC/IF, FACS, ELISA
- 靶点：
alpha Smooth Muscle Actin
- 抗体英文名：
alpha Smooth Muscle Actin antibody [1H8]
- 抗体名：
alpha Smooth Muscle Actin 抗体 [1H8]
- 规格：
100 μl
ELISA analysis of antigen using GTX60393 alpha Smooth Muscle Actin antibody [1H8].
Red : Control antigen 100ng
Purple : Antigen 10ng
Green : Antigen 50ng
Blue : Antigen 100ng
FACS analysis of HeLa cells using GTX60393 alpha Smooth Muscle Actin antibody [1H8].
Green : alpha Smooth Muscle Actin
Purple : negative control
ICC/IF analysis of NIH3T3 cells using GTX60393 alpha Smooth Muscle Actin antibody [1H8].
Green : alpha Smooth Muscle Actin
Blue: DRAQ5 fluorescent DNA dye
WB analysis of HeLa (1), Jurkta (2), HepG2 (3), MCF-7 (4), A431 (5), A549 (6), PC-12 (7), NIH3T3 (8) and Cos7 (9) cell lysate using GTX60393 alpha Smooth Muscle Actin antibody [1H8].
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文献和实验by reaction with alkaline phosphatase-conjugated goat anti-mouse secondary antibody. Choose the actin pool broadly, however, consider also checking the column fractions by dot blot with mAB 3F2 to identify capping protein. Pool the actin fractions
Isolation and Culture of Human Airway Smooth Muscle Cells
doublings and express smooth muscle cell-specific markers such as myosin heavy chain, myosin light chain kinase, α-actin, caldesmon, and SM22α . In addition, the synthetic function of these cells appears to be comparable to those studied in vivo
Fluorescence Procedures for the Actin and Tubulin Cytoskeleton in Fixed Cells
and sensitive to changes in both the chemical and mechanical environment. Optimal conditions for fluorescence of proteins of the actin and tubulin cytoskeleton are based on: preserving cell structure; properties of individual cytoskeletal proteins
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