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- BioLegend
- 116263
- 美国
- 2025年07月14日
- 大鼠
- 小鼠
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- 技术资料
- 抗体名：
APC/Fire™ 810 anti-mouse TER-119/Erythroid Cells
- 抗体英文名：
APC/Fire™ 810 anti-mouse TER-119/Erythroid Cells
- 浓度：
0.2 mg/ml
- 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：
APC/Fire™ 810
- 克隆性：
单克隆
- 保存条件：
2-8度
- 形态：
液体
- 规格：
25ug
APC/Fire™ 810 anti-mouse TER-119/Erythroid Cells Antibody
TER-119
Catalog# / Size 116263 / 25 µg
116264 / 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 APC/Fire™ 810 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
The OP9-DL1 System: Generation of T-Lymphocytes from Embryonic or Hematopoietic Stem Cells In Vitro
.1, Ter119) progenitor cells or HSCs. The sorting step can be expedited by first depleting the Lineage + cells with MACS prior to flow cytometric cell sorting. 74. Seed 2-5 x 105 cells in 10 mL of OP9 medium per 10-cm dish of 80
Introduction Techniques routinely used in our lab for analysing the X-inactivation process in differentiating ES cells are described. We focus particularly on chromatin changes (histone modifications, protein association
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