Anti-Human ATRX/RAD54L Monoclo
nal Antibody (1A571), 抗人ATRX/RAD54L Monoclonal抗体 (1A571)- 询价
- abinScience
- China
- HC152015
- 2026年03月03日
- ELISA, IHC, WB
- Mouse
- Human
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- 详细信息
- 文献和实验
- 技术资料
- 免疫原：
E. coli - derived recombinant human ATRX/RAD54L (Thr1534-Asp1916).
- 亚型：
IgG
- 形态：
Liquid
- 保存条件：
0.01M PBS, pH 7.4.
- 克隆性：
Monoclonal
- 标记物：
Unconjugated
- 适应物种：
Human
- 保质期：
1 year
- 抗原来源：
Mouse
- 目录编号：
HC152015
- 级别：
科研级别
- 库存：
999
- 供应商：
abinScience
- 宿主：
Mouse
- 应用范围：
ELISA, IHC, WB
- 浓度：
1mg/ml
- 靶点：
Transcriptional regulator ATRX, EC:3.6.4.12, ATP-dependent helicase ATRX, X-linked helicase II, X-linked nuclear protein, XNP, Znf-HX, ATRX
- 抗体英文名：
Anti-Human ATRX/RAD54L Monoclonal Antibody (1A571)
- 抗体名：
Anti-Human ATRX/RAD54L Monoclonal Antibody (1A571)
- 规格：
50ug/100ug
| Product name | Anti-Human ATRX/RAD54L Monoclonal Antibody (1A571) |
|---|---|
| Catalog No. | HC152015 |
| Host species | Mouse |
| Species reactivity | Human |
| Immunogen | E. coli - derived recombinant human ATRX/RAD54L (Thr1534-Asp1916). |
| Form | Liquid |
| Storage buffer | 0.01M PBS, pH 7.4. |
| Clonality | Monoclonal |
| Isotype | IgG |
| Applications | ELISA, IHC, WB |
| Target | Transcriptional regulator ATRX, EC:3.6.4.12, ATP-dependent helicase ATRX, X-linked helicase II, X-linked nuclear protein, XNP, Znf-HX, ATRX |
| Purification | Protein A/G purified from cell culture supernatant. |
| Endotoxin level | \ |
| Accession | P46100 |
| Stability and Storage | Use a manual defrost freezer and avoid repeated freeze-thaw cycles. Store at 4°C short term (1-2 weeks). Store at -20°C 12 months. Store at -80°C long term. |
| Clone ID | 1A571 |
| Note | For research use only. |
abinScience, founded in 2023 in Strasbourg, France, is committed to developing and producing high-quality life science reagents. Rooted in one of Europe’s leading hubs for scientific innovation, abinScience empowers global research through reliable, efficient experimental solutions. Guided by the vision of “Empowering Bioscience Discovery,” we support scientists worldwide in advancing the frontiers of bioscience.
Technology and Innovation
Relying on the global leading position in antibody and protein research and more than 20 years of industry experience of its parent company ProteoGenix since 2003, abinScience has inherited advanced technologies and high-quality standards. In particular, the XtenCHO™ system developed by ProteoGenix, which has two modes of transient expression and stable expression, has been widely recognized as a core technology to improve the efficiency of protein production, providing a solid foundation for ab...
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文献和实验• Mutant ATRX: pathogenesis of ATRX syndrome and cancer. PMID: 39479502
• Subcellular Proteomic Mapping of Lysine Lactylation. PMID: 39569522
• Loss of colonic fidelity enables multilineage plasticity and metastasis. PMID: 40468074
• Phase separated condensates of ATRX regulate neural progenitor identity. PMID: 40659667
• Mutations in transcriptional regulator ATRX establish the functional significance of a PHD-like domain. PMID: 9326931
• Localization of a putative transcriptional regulator (ATRX) at pericentromeric heterochromatin and the short arms of acrocentric chromosomes. PMID: 10570185
• Protein UFMylation regulates early events during ribosomal DNA-damage response. PMID: 39277864
• The Multiple Facets of ATRX Protein. PMID: 34062956
Notes on Making Rat x Y3 Monoclonal Antibody Producing Hybridomas
are very stable - even in long term large scale cultures (bioreactors). b) High levels of monoclonal antibody secretion in culture - often 100 micrograms per ml of ordinary tissue culture, without recloning, and up to 5 milligrams per ml in hollow fibre
secondary antibody review -- data from 99 publications
cytometry used as a control to detect cell responses targeted antigen 7 Alexa Fluor 488 7 Cy3 8 goat IgG Alexa Fluor 488 1:2000 detect antibody binding in human embryonic kidney 293T cells Invitrogen 9 donkey
Detection of apoptotic process in situ using immunocytochemical and TUNEL assays
antibody (mAb) conjugated with peroxidase (anti-DNA-POD) was used. This anti-DNA-POD mAb binds to single- and double-stranded, low molecular weight DNA fragments (mono- and oligonucleosomes), showing the internucleosomal degradation of genomic DNA occuring
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