肿瘤坏死因子受体超家族成员1A(TNFRSF1A)多克隆抗体

Polyclonal Antibody to Tumor Necrosis Factor Receptor Superfamily, Member 1A (TNFRSF1A)

CD120A; P55; TBP1; FPF; TNF-R; TNF-R-I; TNF-R55; TNFAR; TNFR1; TNFR55; TNFR60; P55-R; P60; Tumor necrosis factor receptor 1; Tumor necrosis factor-binding protein 1

仅供体外研究使用,不用于临床诊断!警防假冒,可索取进口关税税单及报关单!
  • 肿瘤坏死因子受体超家族成员1A(TNFRSF1A)多克隆抗体 产品包装(模拟)
  • 肿瘤坏死因子受体超家族成员1A(TNFRSF1A)多克隆抗体 产品包装(模拟)
  • 肿瘤坏死因子受体超家族成员1A(TNFRSF1A)多克隆抗体 Figure. DAB staining on IHC-P; Samples: Human Liver Cancer Tissue.
  • 肿瘤坏死因子受体超家族成员1A(TNFRSF1A)多克隆抗体 Figure:FITC staining on IHC-P
    Simple: Hela cells
  • 肿瘤坏死因子受体超家族成员1A(TNFRSF1A)多克隆抗体 Figure. DAB staining on IHC-P; Samples: Human Prostate Gland Tissue.
  • 肿瘤坏死因子受体超家族成员1A(TNFRSF1A)多克隆抗体 Figure. DAB staining on IHC-P; Samples: Human Kidney Tissue.
  • PAB499Hu01.jpg Figure. Western Blot; Sample: Recombinant ADRbK1, Human.
  • Certificate 通过ISO 9001、ISO 13485质量体系认证

特异性

该抗体是针对TNFRSF1A的兔多克隆抗体。在免疫组织化学染色和免疫印迹实验中能识别TNFRSF1A。

用法

Western blotting: 1-5ug/ml
Immunocytochemistry in formalin fixed cells: 5-20ug/ml
Immunohistochemistry in formalin fixed frozen section: 5-20ug/ml
Immunohistochemistry in paraffin section: 5-20ug/ml
Enzyme-linked Immunosorbent Assay: 0.05-2ug/ml
Optimal working dilutions must be determined by end user.

储存

经常使用则4°C保存。-20°C保存不超过一年。避免反复冻融。

稳定性

热稳定性以损失率显示。损失率是由加速降解试验决定,具体方法如下:在37°C孵育48小时,没有显著的降解或者沉淀产生。保质期内,在适当的条件下存储,损失率低于5%。

相关产品

编号 适用物种:Homo sapiens (Human,人) 应用
RPB499Hu01 肿瘤坏死因子受体超家族成员1A(TNFRSF1A)重组蛋白 Positive Control; Immunogen; SDS-PAGE; WB.
APB499Hu01 肿瘤坏死因子受体超家族成员1A(TNFRSF1A)活性蛋白 Cell culture; Activity Assays.
RPB499Hu02 肿瘤坏死因子受体超家族成员1A(TNFRSF1A)重组蛋白 Positive Control; Immunogen; SDS-PAGE; WB.
PAB499Hu01 肿瘤坏死因子受体超家族成员1A(TNFRSF1A)多克隆抗体 WB; IHC; ICC; IP.
PAB499Hu02 肿瘤坏死因子受体超家族成员1A(TNFRSF1A)多克隆抗体 WB; IHC; ICC; IP.
MAB499Hu21 肿瘤坏死因子受体超家族成员1A(TNFRSF1A)单克隆抗体 WB; IHC; ICC; IP.
SEB499Hu 肿瘤坏死因子受体超家族成员1A(TNFRSF1A)检测试剂盒(酶联免疫吸附试验法) Enzyme-linked immunosorbent assay for Antigen Detection.

参考文献

杂志 参考文献
PLoS ONE A Combinatorial Relative Mass Value Evaluation of Endogenous Bioactive Proteins in Three-Dimensional Cultured Nucleus Pulposus Cells of Herniated Intervertebral Discs: Identification of Potential Target Proteins for Gene Therapeutic Approaches [Plosone: Source]
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