| Field | Specification |
|---|---|
| Mfr No | |
| Alternative Names | homolog of B; RAD23B; RD23B_HUMAN; UV excision repair protein RAD23 homolog B; XP C repair complementing complex 58 kDa; XP C repair complementing complex 58 kDa protein; XP C repair complementing protein; XP-C repair-complementing complex 58 kDa protein; |
| Clonality | |
| Conjugate | |
| Form | Liquid |
| Host | |
| Immunogen | Purified recombinant human hHR23b protein fragments expressed in E.coli. |
| Isotype | |
| Product Type | |
| Reactivity | |
| Source | This product is a monoclonal antibody produced from mouse hybridoma cells. |
| Storage | |
| Target | |
| UniProt # |
Overview
This is a monoclonal anti-RAD23B antibody raised in Mouse, with confirmed utility in ELISA, WB, IHC, ICC. It is designed to detect RAD23B protein in Human, Mouse, Rat, Monkey, Hamster and supports researchers working in epigenetics and nuclear signaling contexts.
Key elements and design rationale
- Immunogen: Purified recombinant human hHR23b protein fragments expressed in E.coli. — determines the epitope region; confirm compatibility with sample preparation and expected post-translational modifications.
- Host species (Mouse): Requires anti-mouse-IgG secondary reagents for indirect detection.
- Monoclonal format: Single-epitope binding provides high specificity and lot-to-lot reproducibility. Confirm epitope accessibility under your assay conditions.
- Isotype (IgG2b): Matched secondary antibodies and isotype controls required. Compatible with standard Protein A/G purification workflows.
- Purification (Affinity chromatography): Enriches for specific immunoglobulin classes; reduces non-specific background vs. crude antisera.
Biological background
RAD23B (also referred to as homolog of B, RAD23B, RD23B_HUMAN, UV excision repair protein RAD23 homolog B, XP C repair complementing complex 58 kDa, XP C repair complementing complex 58 kDa protein, XP C repair complementing protein, XP-C repair-complementing complex 58 kDa protein,) is a protein target studied in Human systems. Expression, subcellular localization, and post-translational modifications vary across cell types and disease states — factors critical to antibody-based detection design. Consult UniProt, NCBI Gene, and primary literature for current annotation of RAD23B biology in epigenetics and nuclear signaling.
Common research applications
- ELISA: Quantification of soluble target in biological fluids or culture supernatants. Ensure samples are within the linear detection range.
- WB: Confirms target molecular weight and distinguishes isoforms under denaturing conditions.
- IHC: Visualization of target in FFPE or frozen tissue sections. Optimize antigen retrieval and secondary detection for each tissue type.
- ICC: Subcellular localization in fixed cells or tissue sections; fixation and permeabilization conditions affect epitope accessibility.
Notes for experimental interpretation
- Isotype controls: Use an isotype-matched (IgG2b from Mouse) control at equivalent concentration to assess non-specific background.
- Cross-reactivity: Confirm the clone does not cross-react with related family members under your assay conditions.
- Matrix effects: Sample matrix can affect performance; pilot dilution linearity and spike-recovery experiments are advised for quantitative studies.
- Species reactivity: Confirmed for Human, Mouse, Rat, Monkey, Hamster. Extrapolation to untested species requires empirical validation.
This product is a monoclonal antibody produced from mouse hybridoma cells.
RAD23B is a protein target in Human, Mouse, Rat, Monkey, Hamster biology. This monoclonal antibody raised in Mouse is designed to detect RAD23B in ELISA, WB, IHC, ICC applications, with IgG2b isotype.
Reported reactive against Human, Mouse, Rat, Monkey, Hamster. Immunogen derived from Human. Cross-reactivity with other species should not be assumed without documented data or empirical testing.
Reported for ELISA, WB, IHC, ICC. Each format requires independent dilution optimization and appropriate controls. Unlisted applications require empirical testing.
This non-conjugated IgG2b antibody requires a compatible secondary. Select anti-mouse IgG secondary conjugated to your preferred reporter (HRP, AP, fluorophore, or biotin), matched to IgG2b.
(1) Isotype control — IgG2b from Mouse at matching concentration; (2) Positive control — known RAD23B-expressing cell/tissue; (3) Negative control — knockdown/knockout sample for specificity; (4) Dilution linearity — verify proportional signal decrease in your matrix.
Customization & Add-ons: Can’t find the antibody you need—or require a custom format for your assay? We can help you source the best match or support custom antibody solutions for diverse research needs, including species and isotype selection, conjugations and labeling (e.g., HRP/AP, biotin, fluorophores), purification grade options (Protein A/G, affinity purified), formulation preferences (buffer selection, carrier-free, glycerol-free), custom concentrations and aliquoting, low-endotoxin options for cell-based work, and application-focused QC/validation support (project dependent). Click Talk to a Scientist to submit a request, email us at support@biohippo.com, or explore our Research Services for additional support—our team will follow up with feasibility details and next steps.
