产品特性
C-FOS Antibody
应用：ICC,IF,IHC,WB验证
Host:Rabbit
高文献引用数据支持（通过CiteAb官网可查）
| 规格 | 价格 |
|---|---|
| 100 µL | ￥咨询 |
产品咨询：info@biopcr.com
产品订购：sales@biopcr.com
技术支持：tech@biopcr.com
服务热线：400-860-6200
详细介绍
产品名称：C-FOS抗体
别名：Proto-oncogene c-Fos; Cellular oncogene; G0/G1 switch regulatory protein 7; Proto-oncogene protein; G0S7; p55; AP-1; FBJ murine osteosarcoma viral oncogene homolog, anti-CFOS
宿主：Rabbit
应用：ICC,IF,IHC,WB验证
反应性：Mouse, Rat
形式：Lyophilized Whole Serum
描述：
For induction of c-fos protein activity rats were injected with 1.0 ml of 1.5 M NaCl per 100 grams of body weight. Negative control rats were injected with the same volume of normal saline. The ImmunoStar c-fos antiserum was quality control tested using standard immunohistochemical methods. The antiserum demonstrates strongly positive labeling of rat paraventricular nucleus and supraoptic nucleus using indirect immunofluorescent and biotin/avidin-HRP techniques. No labeling was seen in negative control rats. Recommended primary dilutions for these methods are 1/4000-1/6000 in PBS/0.3% Triton X-100 – FITC Technique and 1/4000-1/6000 in PBS/0.3% Triton X-100 – biotin/avidin-HRP Technique.
Injection of intraperitoneal hypertonic saline to provoke fos expression is most usually used to set ICC staining parameters. It is critical that tissue is harvested 60-90 minutes post injection for this and any other stress that is used. Inject 1 ml/100 g body weight 1.5 M NaCl intraperitoneally. Harvest brains 90 minutes post injection. Time is critical.
Specificity of the antiserum was demonstrated by blockage of staining in experimental rats by omission of c-fos antibody or by substitution of antibody pre-incubated with synthetic peptide or the conjugate. Immunoblot analysis of mediobasal hypothalamus showed a single band of approximately 55-60 kD.
图片说明：
IHC image of neurons staining for c-Fos in the rat supraoptic nucleus. The tissue was fixed with 4% formaldehyde in 0.1 M phosphate buffer, before being removed and prepared for vibratome sectioning. Floating sections were incubated at RT in 10% goat serum in PBS, before standard IHC procedure. Primary antibody was incubated at 1:5000 for 48 hours, goat anti-rabbit secondary was subsequently added for 1 hour after washing with PBS. Light microscopy staining was achieved with standard biotin-streptavidin/HRP procedure and DAB chromogen. The section was then mounted on slides with permount.
RRID：AB_572267
GeneSymbol：FOS
运输条件：Blue ice
返回列表
For induction of c-fos protein activity rats were injected with 1.0 ml of 1.5 M NaCl per 100 grams of body weight. Negative control rats were injected with the same volume of normal saline. The ImmunoStar c-fos antiserum was quality control tested using standard immunohistochemical methods. The antiserum demonstrates strongly positive labeling of rat paraventricular nucleus and supraoptic nucleus using indirect immunofluorescent and biotin/avidin-HRP techniques. No labeling was seen in negative control rats. Recommended primary dilutions for these methods are 1/4000-1/6000 in PBS/0.3% Triton X-100 – FITC Technique and 1/4000-1/6000 in PBS/0.3% Triton X-100 – biotin/avidin-HRP Technique.
Injection of intraperitoneal hypertonic saline to provoke fos expression is most usually used to set ICC staining parameters. It is critical that tissue is harvested 60-90 minutes post injection for this and any other stress that is used. Inject 1 ml/100 g body weight 1.5 M NaCl intraperitoneally. Harvest brains 90 minutes post injection. Time is critical.
Specificity of the antiserum was demonstrated by blockage of staining in experimental rats by omission of c-fos antibody or by substitution of antibody pre-incubated with synthetic peptide or the conjugate. Immunoblot analysis of mediobasal hypothalamus showed a single band of approximately 55-60 kD.
图片说明：
IHC image of neurons staining for c-Fos in the rat supraoptic nucleus. The tissue was fixed with 4% formaldehyde in 0.1 M phosphate buffer, before being removed and prepared for vibratome sectioning. Floating sections were incubated at RT in 10% goat serum in PBS, before standard IHC procedure. Primary antibody was incubated at 1:5000 for 48 hours, goat anti-rabbit secondary was subsequently added for 1 hour after washing with PBS. Light microscopy staining was achieved with standard biotin-streptavidin/HRP procedure and DAB chromogen. The section was then mounted on slides with permount.
RRID：AB_572267
GeneSymbol：FOS
运输条件：Blue ice
