- ￥5300
- GeneTex
- 美国
- GTX29751
- 2025年07月15日
- WB, ELISA, Neutralizing/Inhibition, Sandwich ELISA
- Rabbit
- Mouse
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- 详细信息
- 文献和实验
- 技术资料
- 免疫原：
Produced from sera of rabbits pre-immunized with highly pure (>98%) recombinant mG-CSF.
- 亚型：
IgG
- 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：
Polyclonal
- 标记物：
Unconjugated
- 适应物种：
Mouse
- 保质期：
12 months from the shipping date of the product.
- 抗原来源：
Mouse
- 目录编号：
GTX29751
- 级别：
Primary Antibodies
- 库存：
Available
- 供应商：
GeneTex
- 宿主：
Rabbit
- 应用范围：
WB, ELISA, Neutralizing/Inhibition, Sandwich ELISA
- 浓度：
Batch dependent (Please refer to the vial label for the specific concentration.)
- 靶点：
G-CSF
- 抗体英文名：
G-CSF antibody
- 抗体名：
G-CSF 抗体
- 规格：
50 μg
WB analysis of sequential diluted mouse G-CSF under either reducing or non-reducing conditions using GTX29751 G-CSF antibody.
Working concentration : 0.1 - 0.2 ug/ml
ELISA analysis of mouse G-CSF recombinant protein(0.2 - 0.4 ng/well) using GTX29751 G-CSF antibody(capture antibody) at 0.5 - 2.0 ug/ml and Biotinylated Anti-Murine G-CSF as a detection antibody.
WB analysis of sequential diluted mouse G-CSF under either reducing or non-reducing conditions using GTX29751 G-CSF antibody.
Working concentration : 0.1 - 0.2 ug/ml
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文献和实验Hematopoietic Stem Cell Mobilization with G-CSF
stem cells are collected after G-CSF administration. In this chapter we describe peripheral blood stem cell mobilization in autologous transplant patients and in allogeneic donors using G-CSF.
Hematopoietic Stem Cell Mobilization with Agents Other than G-CSF
factor (G-CSF) are the preferred source for transplantation. G-CSF mobilization regimens, however, are associated with known morbidities and a significant number of normal donors and patient populations fail to mobilize sufficient numbers of hematopoietic
Generation of Antibody Molecules Through Antibody Engineering
been overcome to a large extent using genetic-engineering techniques to produce chimeric mouse/human and completely human antibodies. Such an approach is particularly suitable because of the domain structure of the antibody molecule ( 2 ), where functional
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