- ￥4603
- BioLegend
- 116228
- 美国
- 2025年07月16日
- 免疫荧光，流式
- 大鼠
- 小鼠
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- 详细信息
- 文献和实验
- 技术资料
- 抗体名：
PerCP/Cyanine5.5 anti-mouse TER-119/Erythroid Cells
- 抗体英文名：
PerCP/Cyanine5.5 anti-mouse TER-119/Erythroid Cells
- 浓度：
0.2 mg/ml
- 应用范围：
免疫荧光，流式
- 宿主：
大鼠
- 供应商：
上海善然生物
- 库存：
现货
- 抗原来源：
大鼠
- 保质期：
2-3年左右
- 适应物种：
小鼠
- 标记物：
PerCP/Cyanine5.5
- 克隆性：
单克隆
- 规格：
100 μg
PerCP/Cyanine5.5 anti-mouse TER-119/Erythroid Cells Antibody
TER-119
Catalog# / Size 116227 / 25 µg
116228 / 100 µg
Clone
Regulatory Status RUO
Other Names Ly-76
Isotype Rat IgG2b, κ
Description The TER-119 antigen is a 52 kD glycophorin A-associated protein, also known as Ly-76. TER119 is an erythroid-specific antigen expressed on early proerythroblasts to mature
erythrocytes, but not on erythroid colony-forming cells (BFU-E, blast-forming unit erythroid, or
CFU-E, colony-forming unit erythroid).
Product Details
Verified Reactivity Mouse
Antibody Type Monoclonal
Host Species Rat
Immunogen Day-14 fetal liver cells from a C57BL/6 mouse
Formulation Phosphate-buffered solution, pH 7.2, containing 0.09% sodium azide.
Preparation The antibody was purified by affinity chromatography, and conjugated with PerCP/Cyanine5.5
under optimal conditions.
Concentration 0.2 mg/ml
Storage & Handling The antibody solution should be stored undiluted between 2°C and 8°C, and protected from
prolonged exposure to light. Do not freeze.
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STM：傅阳心、侯玉柱等发现放疗与免疫治疗的交汇点，兵家必争之地竟是这群细胞
细胞或外源性注射 ARTN 同样可以减弱放疗和 PD-L1 阻滞的抗肿瘤作用。上述的结果表明免疫治疗和放疗的治疗作用部分依赖于它们对 Ter 细胞的抑制。 图片来源：Sci. Transl. Med 同样的，破坏 Ter/ARTN 轴能够恢复甚至增加放疗和抗 PD-L1 治疗的疗效。通过使用 anti-Ter119 抗体，将小鼠体内 Ter 细胞耗尽，这显著促进了放疗和抗 PD-L1 治疗的作用。接下来的研究也表明阻断 ARTN 能增强抗肿瘤治疗效果。因此，Ter 细胞耗尽、ARTN 中和都能够
for nutrient and waste exchange between the fetus and its mother. The trophoblast can be modeled in vitro using trophoblast stem cells. Trophoblast stem cells require fibroblast growth factor (FGF)4, heparin, and contact with embryonic fibroblasts
RNAse A Treatment of Mouse Cells
-HP1 antibodies at pericentromeric regions. Triton X-100-permeabilized L929 cells were treated with RNAse A (+RNAse) or mock-treated (-RNAse) before paraformaldehyde fixation. Double-labeling immunofluorescence was carried out using anti-HP
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