- ￥7800
- GeneTex
- 美国
- GTX20286
- 2025年07月16日
- WB
- Llama
- Mouse
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- 详细信息
- 文献和实验
- 技术资料
- 免疫原：
ChromPure Mouse IgG, whole molecule
- 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. Protect from light.
- 克隆性：
Polyclonal
- 标记物：
FITC
- 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：
GTX20286
- 级别：
Secondary Antibodies
- 库存：
Available
- 供应商：
GeneTex
- 宿主：
Llama
- 应用范围：
WB
- 浓度：
Batch dependent (Please refer to the vial label for the specific concentration.)
- 靶点：
Llama Anti-mouse IgG
- 抗体英文名：
Llama Anti-mouse IgG antibody (FITC)
- 抗体名：
Llama Anti-mouse IgG 抗体 (FITC)
- 规格：
250 μg
WB analysis of mouse IgG recombinant protein using GTX20286 Llama Anti-mouse IgG antibody (FITC).
Lane 1 : Non-Reduced Mouse IgG probed with Llama IgG1, G2, G3 anti-mouse IgG
Lane 2 : Reduced Mouse IgG probed with Llama IgG1, G2, G3 anti-mouse IgG
Lane 3 : Reduced Mouse IgG probed with Llama IgG1 Fraction anti-mouse IgG
Lane 4 : Reduced Mouse IgG probed with Llama IgG2 Fraction anti-mouse IgG
Lane 5 : Reduced Mouse IgG probed with Llama IgG3 Fraction anti-mouse IgG
GTX20286 Llama Anti-mouse IgG antibody (FITC) was analyzed on 10% SDS-PAGE under non-reduced (I) and reduced conditions(II).
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文献和实验Anticardiolipin Antibody and Anti-beta 2 Glycoprotein I Antibody Assays
standard” laboratory test to diagnose or classify a patient as having APS. This chapter discusses the clinical and laboratory theoretical and technical aspects of aCL and anti-β2GPI antibody assays.
4-Hydroxy-2-Nonenal (4-HNE) Staining by Anti-HNE Antibody
using an anti-4-HNE monoclonal antibody (MAb) (6 –8 ) and labeled goat anti-mouse IgG antibody (9 ).
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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