![TAG-72 Antibody [SPM536] 抗体，orb1251944，Biorbyt产品图](https://img1.dxycdn.com/p/s14/2026/0729/505/4876880692122632802.jpg)
- ￥13338
- Biorbyt
- orb1251944
- 英国
- 2026年07月31日
- FC, IF, IHC
- Mouse
- Bovine, Canine, Human, Rat
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- 文献和实验
- 技术资料
- 抗体名：
TAG-72 Antibody [SPM536] 抗体
- 抗体英文名：
TAG-72 Antibody [SPM536]
- 浓度：
0.2 mg/mL
- 应用范围：
FC, IF, IHC
- 宿主：
Mouse
- 适应物种：
Bovine, Canine, Human, Rat
- 保质期：
12 months from date of receipt.
- 抗原来源：
详询
- 目录编号：
orb1251944
- 级别：
科研
- 库存：
99
- 供应商：
Biorbyt
- 标记物：
Unconjugated
- 克隆性：
Monoclonal
- 保存条件：
详询
- 形态：
Liquid
- 亚型：
IgG1, kappa
- 免疫原：
详询
- 规格：
100 ug
产品子类型: Primary Antibody
描述: TAG-72 Antibody [SPM536]
克隆号: SPM536
应用说明: Flow Cytometry: 0.5-1 ug/million cells in 0.1mlImmunofluorescence: 1-2 µg/mLImmunohistochemistry (FFPE): 0.5-1 µg/mL for 30 minutes at RT (1)Prediluted format: incubate for 30 min at RT (2)The optimal dilution of the TAG-72 antibody for each application should be determined by the researcher.1. Staining of formalin-fixed tissues requires boiling tissue sections in 10mM citrate buffer, pH 6.0, for 10-20 min followed by cooling at RT for 20 minutes.2. The prediluted format is supplied in a dropper bottle and is optimized for use in IHC. After epitope retrieval step (if required), drip mAb solution onto the tissue section and incubate at RT for 30 min.
免疫原: Purified TAG-72 protein was used as the immunogen for this TAG-72 antibody.
防腐剂: PBS with 0.1 mg/ml rAlbumin and 0.05% sodium azide
纯化方法: Protein G affinity chromatography
研究领域: Cancer Biology, Signal Transduction
保存条件: Maintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles.
备注: For research use only.
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文献和实验Isolation of Human Fab Fragments Against Ovarian Carcinoma Using Guided Selection
on aspects such as mechanisms of action, preclinical screening, and clinical results, see specific references in Table 1 and an excellent recent review (1 ). Table 1 Target Antigens Potentially Suited for Antibody-Based Immunotherapy of Ovarian
Preparing Colloidal Gold for Electron Microscopy
and 0.1 where there is no significant background. If using a primary antibody then the optimal dilution of this first antibody must be known. Sections can be treated with protein A gold alone to determine the background labelling. Table 1:
Using Phospho‐Motif Antibodies to Determine Kinase Substrates
comprising both the phosphorylated residue and the surrounding residues that determine kinase specificity, with degenerate residues taking up the remaining positions. Currently, several categories of phospho?motif antibody are commercially available
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