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- 详细信息
- 文献和实验
- 技术资料
- 免疫原:
Recombinant protein encoding amino acids 1-140 of the large subunit of human DNA polymerase d.
- 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:
GTX77606
- 级别:
Primary Antibodies
- 库存:
Available
- 供应商:
GeneTex
- 宿主:
Mouse
- 应用范围:
WB, IHC-P
- 浓度:
1.22 mg/ml (Please refer to the vial label for the specific concentration.)
- 靶点:
DNA polymerase delta
- 抗体英文名:
DNA polymerase delta antibody [6196]
- 抗体名:
DNA polymerase delta 抗体 [6196]
- 规格:
100 μl
Whole cell extract (30 μg) was separated by 5% SDS-PAGE, and the membrane was blotted with DNA polymerase delta antibody [6196] (GTX77606) diluted at 1:1000.
DNA polymerase delta antibody [6196] detects DNA polymerase delta protein at cytoplasm and nucleus by immunohistochemical analysis.
Sample: Paraffin-embedded human colon cancer.
DNA polymerase delta stained by DNA polymerase delta antibody [6196] (GTX77606) diluted at 1:200.
Antigen Retrieval: Citrate buffer, pH 6.0, 15 min
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文献和实验Molecular Manipulations of the Catalytic RNAs from the Human Hepatitis Delta Virus
that is replicated by a rolling-circle mechanism (reviewed by refs. 1 and 2 ). There is no DNA intermediate. The infectious genomic strand is a template for an RNA-dependent RNA polymerase (most likely a modified activity of the host’s RNA polymerase II
Antibody Screening of Bacteriophage gt11 DNA Expression Libraries
from one species, it can be used to probe cDNA libraries from other species using DNA hybridization techniques. Alternatively, degenerate oligonucleotides can be designed from amino acid sequences from regions of proteins that are conserved across species
Antibody Screening of Bacteriophage gt-11 DNA Expression Libraries
from one species, it can be used to probe cDNA libraries from other species using DNA hybridization techniques. Alternatively, degenerate oligonucleotides can be designed from amino acid sequences from regions of proteins that are conserved across species
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