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- 详细信息
- 文献和实验
- 技术资料
- 免疫原:
A synthetic peptide corresponding to a sequence in the middle region of human Thrombospondin 2(637-655aa EAAKTEKQVCEPENPCKDK), different from the mouse sequence by two amino acids.
- 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:
Human, Mouse, Rat
- 保质期:
12 months from the shipping date of the product.
- 抗原来源:
Human
- 目录编号:
GTX11699
- 级别:
Primary Antibodies
- 库存:
Available
- 供应商:
GeneTex
- 宿主:
Rabbit
- 应用范围:
WB, ICC/IF, IHC-P, IHC-Fr, FACS
- 浓度:
500 μg/ml (Please refer to the vial label for the specific concentration.)
- 靶点:
Thrombospondin 2
- 抗体英文名:
Thrombospondin 2 antibody
- 抗体名:
Thrombospondin 2 抗体
- 规格:
100 μg
WB analysis of various samples using GTX11699 Thrombospondin 2 antibody.
Lane 1 : human HeLa whole cell lysates
Lane 2 : human 22RV1 whole cell lysates
Lane 3 : human U-87MG whole cell lysates
Lane 4 : human THP-1 whole cell lysates
Lane 5 : human PC-3 whole cell lysates
Lane 6 : human Caco-2 whole cell lysates
Dilution : 0.5 μg/mL
Loading : 50μg of sample under reducing conditions
FACS analysis of U87-MG cells using GTX11699 Thrombospondin 2 antibody.
Blue : Primary antibody
Green : Isotype control
Red : Cell only control
Antibody amount : 1μg/1x10⁶ cells for 30 min at 20ºC
IHC-P analysis of human placenta tissue using GTX11699 Thrombospondin 2 antibody.
Antigen retireval : Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins
Dilution : 1μg/ml
WB analysis of various samples using GTX11699 Thrombospondin 2 antibody.
Lane 1 : rat brain tissue lysates
Lane 2 : mouse brain tissue lysates
Dilution : 0.5 μg/mL
Loading : 50μg of sample under reducing conditions
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文献和实验Development of techniques for primary culture of C. elegans embryonic neurons
detailed studies of the interactions of growing axons with their substrates are possible, including antibody perturbation studies of cell-surface molecules, direct observation of growth cone behavior, and pharmacological manipulation of growing
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