- ￥5600
- GeneTex
- 美国
- GTX60630
- 2025年06月29日
- WB, ICC/IF, IHC-P, FACS, ELISA
- Mouse
- Human
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- 详细信息
- 文献和实验
- 技术资料
- 免疫原：
Purified recombinant fragment of human IGF2 (AA: 25-180) expressed in E. Coli.
- 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
- 保质期：
12 months from the shipping date of the product.
- 抗原来源：
Human
- 目录编号：
GTX60630
- 级别：
Primary Antibodies
- 库存：
Available
- 供应商：
GeneTex
- 宿主：
Mouse
- 应用范围：
WB, ICC/IF, IHC-P, FACS, ELISA
- 浓度：
1 mg/ml (Please refer to the vial label for the specific concentration.)
- 靶点：
IGF2
- 抗体英文名：
IGF2 antibody [8H1]
- 抗体名：
IGF2 抗体 [8H1]
- 规格：
100 μg
IHC-P analysis of ovarian cancer tissue using GTX60630 IGF2 antibody [8H1].
ICC/IF analysis of HeLa cells using GTX60630 IGF2 antibody [8H1].
Green : IGF2
Blue: DRAQ5 fluorescent DNA dye
Red: Actin filaments
IHC-P analysis of bladder cancer tissue using GTX60630 IGF2 antibody [8H1].
WB analysis of HEK293 (1) and IGF2 (AA: 25-180)-hIgGFc transfected HEK293 (2) cell lysate using GTX60630 IGF2 antibody [8H1].
FACS analysis of HepG2 cells using GTX60630 IGF2 antibody [8H1].
Green : IGF2
Red : negative control
ELISA analysis of antigen using GTX60630 IGF2 antibody [8H1].
Black : Control antigen 100ng
Purple : Antigen 10ng
Blue : Antigen 50ng
Red : Antigen 100ng
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文献和实验Hsu CF et al., EBioMedicine 2019 (PMID:30852161)
Mini-Antibody Affinity Chromatography of Lysozyme
Multiple noncovalent forces do play a role in the binding between a protein antigen and an antibody directed against that protein. An antigen is bound by the antigen binding site of an antibody that consists of three hypervariable segments
nm23 Protein Expression by Western Blotting in Patients with Epithelial Ovarian Carcinoma
(4 ), they retain most of the same epitopes; thus any polyclonal antibody raised against one of the two isoforms or a monoclonal antibody against a conserved epitope will recognize both nm23-H1 and -H2 at the same time. Analysis by immunohistochemistry
Extraction of Nuclear Proteins
of approx 20 �m. The nuclear proteins were prepared from the purified nuclei using lysis buffer (3 ) or SDS sample buffer (4 ). The purity of the isolated nuclear fraction was evaluated by Western blot analysis using antihistone H1 antibody, a specific
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