- ￥5000
- GeneTex
- 美国
- GTX34120
- 2026年03月09日
- IHC-P
- Mouse
- Human, Mouse, Rat
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- 详细信息
- 文献和实验
- 技术资料
- 免疫原：
Synthetic Peptide
- 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
- 保质期：
12 months from the shipping date of the product.
- 抗原来源：
Human
- 目录编号：
GTX34120
- 级别：
Primary Antibodies
- 库存：
Available
- 供应商：
GeneTex
- 宿主：
Mouse
- 应用范围：
IHC-P
- 浓度：
Batch dependent (Please refer to the vial label for the specific concentration.)
- 靶点：
Progesterone Receptor
- 抗体英文名：
Progesterone Receptor antibody [Z15]
- 抗体名：
Progesterone Receptor 抗体 [Z15]
- 规格：
100 μl
IHC-P analysis of human liver cancer tissue using GTX34120 Progesterone Receptor antibody [Z15]. Negative control (the lower left coner) was secondary antibody only.
Antigen retrieval : Sodium citrate pH6.0 was used for antibody retrieval (>98ºC, 20min)
Dilution : 1:200
IHC-P analysis of human stomach cancer tissue using GTX34120 Progesterone Receptor antibody [Z15]. Negative control (the lower left coner) was secondary antibody only.
Antigen retrieval : Sodium citrate pH6.0 was used for antibody retrieval (>98ºC, 20min)
Dilution : 1:200
IHC-P analysis of mouse liver tissue using GTX34120 Progesterone Receptor antibody [Z15]. Negative control (the lower left coner) was secondary antibody only.
Antigen retrieval : Sodium citrate pH6.0 was used for antibody retrieval (>98ºC, 20min)
Dilution : 1:200
IHC-P analysis of mouse colon tissue using GTX34120 Progesterone Receptor antibody [Z15]. Negative control (the lower left coner) was secondary antibody only.
Antigen retrieval : Sodium citrate pH6.0 was used for antibody retrieval (>98ºC, 20min)
Dilution : 1:200
IHC-P analysis of human uterus tissue using GTX34120 Progesterone Receptor antibody [Z15]. Negative control (the lower left coner) was secondary antibody only.
Antigen retrieval : Sodium citrate pH6.0 was used for antibody retrieval (>98ºC, 20min)
Dilution : 1:200
IHC-P analysis of human stomach tissue using GTX34120 Progesterone Receptor antibody [Z15]. Negative control (the lower left coner) was secondary antibody only.
Antigen retrieval : Sodium citrate pH6.0 was used for antibody retrieval (>98ºC, 20min)
Dilution : 1:200
IHC-P analysis of rat testis tissue using GTX34120 Progesterone Receptor antibody [Z15]. Negative control (the lower left coner) was secondary antibody only.
Antigen retrieval : Sodium citrate pH6.0 was used for antibody retrieval (>98ºC, 20min)
Dilution : 1:200
IHC-P analysis of rat kidney tissue using GTX34120 Progesterone Receptor antibody [Z15]. Negative control (the lower left coner) was secondary antibody only.
Antigen retrieval : Sodium citrate pH6.0 was used for antibody retrieval (>98ºC, 20min)
Dilution : 1:200
IHC-P analysis of human colon tissue using GTX34120 Progesterone Receptor antibody [Z15]. Negative control (the lower left coner) was secondary antibody only.
Antigen retrieval : Sodium citrate pH6.0 was used for antibody retrieval (>98ºC, 20min)
Dilution : 1:200
IHC-P analysis of rat brain tissue using GTX34120 Progesterone Receptor antibody [Z15]. Negative control (the lower left coner) was secondary antibody only.
Antigen retrieval : Sodium citrate pH6.0 was used for antibody retrieval (>98ºC, 20min)
Dilution : 1:200
IHC-P analysis of human appendix tissue using GTX34120 Progesterone Receptor antibody [Z15]. Negative control (the lower left coner) was secondary antibody only.
Antigen retrieval : Sodium citrate pH6.0 was used for antibody retrieval (>98ºC, 20min)
Dilution : 1:200
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文献和实验Human progesterone receptor (PR) is a member of the nuclear hormone receptor superfamily of transcriptional activators, which share a common modular structure consisting of a C-terminal ligand-binding domain (LBD), a highly conserved
Several assays exist to determine receptor status in ovarian cancers, like radio ligand binding assays, biochemical analysis, and even Northern blotting. However, patholo- gists generally prefer to judge the presence of biological markers
Steroid hormones, such as estrogen, progesterone, androgens, glucocorticoids, and mineralocorticoids, are well-known regulators of the expression of specific gene networks in higher eukaryotes (1 –3 ). The hormonal action is mediated
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