
Thermo Fisher Scientific Phospho-Histone H2A.X (Ser139) Recombinant Mouse Monoclonal Antibody (CR55T33), Alexa Fluor Plus 555
Alexa Fluor Plus 555 형광이 결합된 recombinant mouse monoclonal anti-Phospho-Histone H2A.X (Ser139) 항체. Western blot 및 유세포분석(Flow cytometry)에 적합. 밝은 형광 신호와 일관된 로트 간 재현성 제공. DNA 손상 반응 연구에 활용 가능.
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Applications and Tested Dilution
| Application | Tested Dilution |
|---|---|
| Western Blot (WB) | 1:500 |
| Flow Cytometry (Flow) | 0.5 µg/test |
Product Specifications
| 항목 | 내용 |
|---|---|
| Species Reactivity | Human |
| Host / Isotype | Mouse / IgG1, kappa |
| Expression System | Expi293 |
| Class | Recombinant Monoclonal |
| Type | Antibody |
| Clone | CR55T33 |
| Conjugate | Alexa Fluor™ Plus 555 |
| Excitation / Emission Max | 558 / 572 nm |
| Form | Liquid |
| Concentration | 1.0 mg/mL |
| Purification | Protein A/G |
| Storage Buffer | Proprietary buffer, pH 6.8 |
| Contains | 0.008% Bromonitrodioxane, 0.008% Methylisothiazolone |
| Storage Conditions | 4°C, store in dark, DO NOT FREEZE |
| Shipping Conditions | Wet ice |
Additional Formats:
Product Specific Information
Alexa Fluor™ Plus recombinant antibodies utilize advanced dye chemistry for superior brightness and signal-to-noise ratio compared to conventional Alexa Fluor™ conjugates. As recombinant antibodies, they offer improved specificity and lot-to-lot consistency through controlled gene cloning and expression in vitro.
Usage Note:
Before use, briefly centrifuge the conjugate solution and use only the supernatant to minimize nonspecific background from potential aggregates.
Applications Tested:
This antibody (CR55T33) has been validated by Western blot and flow cytometry using Jurkat cells treated with 50 µM etoposide for 8 hours. Recommended starting concentrations:
- Western blot: 2 µg/mL (optimize per assay)
Optical Properties:
- Excitation: 553 nm
- Emission: 568 nm
- Laser: Yellow Laser
- Filtration: 0.2 µm post-manufacturing filtered
Target Information
Histone H2A.X (H2AX) is a member of the histone H2A family, one of the four core histones forming the nucleosome core particle. Phosphorylation at serine 139 (γ-H2AX) marks sites of DNA double-strand breaks (DSBs) and can be detected by Western blot or immunofluorescence to assess DNA damage frequency.
Phosphorylation is mediated by phosphatidylinositol 3-kinases, potentially including ATM, DNA-PK, and ATR. H2A.X contains 143 amino acids and exists in two mRNA forms (~1600 bases with polyA and ~575 bases without). The gene maps to human chromosome 11q23.2–q23.3 and plays a key role in chromatin structure and DNA repair by recruiting MDC1 to damage sites.
For Research Use Only.
Not for use in diagnostic procedures or resale without authorization.
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