- ￥5000
- GeneTex
- 美国
- GTX65948
- 2025年07月13日
- WB, IHC-P
- Rabbit
- Human, Mouse, Rat
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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 within amino acids 150-250 of human SNRNP70 (NP_003080.2).
- 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：
GTX65948
- 级别：
Primary Antibodies
- 库存：
Available
- 供应商：
GeneTex
- 宿主：
Rabbit
- 应用范围：
WB, IHC-P
- 浓度：
Batch dependent (Please refer to the vial label for the specific concentration.)
- 靶点：
U1 snRNP70
- 抗体英文名：
U1 snRNP70 antibody
- 抗体名：
U1 snRNP70 抗体
- 规格：
100 μl
IHC-P analysis of human cervix cancer tissue using GTX65948 U1 snRNP70 antibody.
Dilution : 1:100
IHC-P analysis of rat testis tissue using GTX65948 U1 snRNP70 antibody.
Dilution : 1:100
IHC-P analysis of mouse kidney tissue using GTX65948 U1 snRNP70 antibody.
Dilution : 1:100
WB analysis of various sample lysates using GTX65948 U1 snRNP70 antibody. The signal was developed with ECL plus-Enhanced.
Dilution : 1:1000
Loading : 25μg per lane
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文献和实验8 The Recovery of Immunoglobulin Sequences from Single Human B Cells by Clonal Expansion
The development of phage-display technology and the construction of huge libraries of antibody (Ab ) fragments have provided an unlimited source of binders to virtually any antigen (Ag ) (1 ). However, it is unlikely that the heavy (VH
further using protein–RNA interactions known to exist in the U1 snRNP. The results indicate that the RIP assay is a powerful tool to identify RNA–protein interactions in vivo and has the potential to unravel the cellular network of RNP complexes in their native
. Biochemistry 22:4546‐4550. Ferre‐D'Amare, A.R. 2010. Use of the spliceosomal protein U1A to facilitate crystallization and structure determination of complex RNAs. Methods 52:159‐167
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