- ￥6100
- GeneTex
- 美国
- GTX13582
- 2025年07月14日
- WB, ICC/IF, IHC-P, FACS, ChIP assay
- Mouse
- Human, Mouse, Rat
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- 详细信息
- 询价记录
- 文献和实验
- 技术资料
- 免疫原：
A bacterially expressed fusion protein containing amino acid residues 1-317 of mouse TRANCE was used as immunogen.
- 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：
Mouse
- 目录编号：
GTX13582
- 级别：
Primary Antibodies
- 库存：
Available
- 供应商：
GeneTex
- 宿主：
Mouse
- 应用范围：
WB, ICC/IF, IHC-P, FACS, ChIP assay
- 浓度：
1 mg/ml (Please refer to the vial label for the specific concentration.)
- 靶点：
sRANKL
- 抗体英文名：
sRANKL antibody [12A668]
- 抗体名：
sRANKL 抗体 [12A668]
- 规格：
100 μg
ICC/IF analysis of mouse splenocytes using GTX13582 sRANKL antibody [12A668].
Red : primary antibody
Blue : DAPI
Dilution : 20 μg/mL
WB analysis of human lymph node tissue lysate (in RIPA buffer) using GTX13582 sRANKL antibody [12A668].
Loading : 35μg
Dilution : 0.5 μg/ml
IHC-P analysis of human lymph node tissue using GTX13582 sRANKL antibody [12A668].
Dilution : 5 μg/ml
Antigen retrieval : 10 mM sodium citrate buffer, pH 6.0
IHC-P analysis of human liver tissue using GTX13582 sRANKL antibody [12A668].
Dilution : 1 μg/ml
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- 作者
- 内容
- 询问日期
文献和实验Immunoprecipitation of PDE2 Phosphorylated and Inactivated by an Associated Protein Kinase
with a protein kinase regulating its activity in an adenosine triphosphate-dependent manner. When native or recombinant PDE2 is immunoprecipitated from PC12 cells using an antibody to the amino terminus in a buffer containing Lubrol 12A9, protease inhibitors
中科院高福院士课题组 2019 年发表了哪些重要的研究成果？
inhibition of CRISPR-Cas12a by AcrVA4（AcrVA4 对 CRISPR-Cas12a 多级抑制的结构研究）原核生物利有 CRISPR-Cas 系统来排除寄生捕食者，如噬菌体和移动遗传元件 (MGEs)。反过来，这些捕食者编码抗 CRISPR (Acr) 蛋白以逃避 CRISPR-Cas 免疫。有研究表明，一种抑制 CRISPR-Cas12a 系统的 Acr 蛋白——AcrVA4 被证明可以减少人纤毛杆菌科细菌 Cas12a（LbCas12a）介导的人类细胞基因组编辑，但其潜在
Detection Of Cell Viability And/Or Apoptosis By Flow Cytometry (FACS)
-specifically bind a fluorescent secondary antibody, the antigen being detected may have been degraded, etc. Non-viable cells tend to have reduced FSC (can be high in case of swollen necrotic cells) but higher SSC values. Because of membrane permeability
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