
Thermo Fisher Scientific POLR2A Monoclonal Antibody (OTI2B7), TrueMAB
POLR2A 단백질을 인식하는 Mouse IgG1 단일클론 항체로, Western blot 및 IHC(P) 검증 완료. 인간, 마우스, 랫트 반응성. 동결건조 형태로 제공되며, 재구성 후 1 mg/mL 농도 유지. 연구용으로 RNA polymerase II 관련 단백질 분석에 적합.
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Applications and Tested Dilution
| Application | Tested Dilution |
|---|---|
| Western Blot (WB) | 1:500 |
| Immunohistochemistry (Paraffin) (IHC (P)) | 1:500 |
Product Specifications
| Specification | Description |
|---|---|
| Species Reactivity | Human, Mouse, Rat |
| Host/Isotype | Mouse / IgG1 |
| Class | Monoclonal |
| Type | Antibody |
| Clone | OTI2B7 |
| Immunogen | Human recombinant protein fragment corresponding to amino acids 1351–1614 of human POLR2A produced in E. coli |
| Conjugate | Unconjugated |
| Form | Lyophilized |
| Concentration | 1 mg/mL |
| Purification | Affinity chromatography |
| Storage Buffer | PBS, pH 7.3, with 8% trehalose |
| Contains | No preservative |
| Storage Conditions | -20°C, Avoid Freeze/Thaw Cycles |
| Shipping Conditions | Ambient (domestic); Wet ice (international) |
Product Specific Information
For reconstitution, add 100 µL of distilled water to achieve a final antibody concentration of approximately 1 mg/mL.
For conjugation experiments, perform an additional desalting step using Zeba Spin Desalting Columns (7K MWCO, 0.5 mL, Product #89882).
Target Information
DNA-directed RNA polymerase II subunit RPB1 (POLR2A) is a DNA-dependent RNA polymerase that catalyzes transcription of DNA into RNA using ribonucleoside triphosphates as substrates.
POLR2A is the largest subunit and a catalytic component of RNA polymerase II, responsible for synthesizing mRNA precursors and various functional non-coding RNAs.
It forms the polymerase active center with the second largest subunit and is integral to the basal transcription machinery. The enzyme includes mobile elements that move relative to each other, with RPB1 forming the core structure containing the large cleft, clamp, and jaws that interact with the DNA template.
Transcription initiation involves positioning the single-stranded DNA template within the central active site cleft. A bridging helix from RPB1 promotes translocation of Pol II by acting as a ratchet mechanism during nucleotide addition.
During elongation, Pol II progresses along the template as the transcript extends. This process is regulated by phosphorylation of the C-terminal domain (CTD) of RPB1, which serves as a scaffold for factors controlling initiation, elongation, termination, and mRNA processing. Gene expression regulation depends on the balance of methylation and acetylation of CTD lysines.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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