MPO Monoclonal Antibody

What it means: Monoclonal antibodies originate from a single hybridoma clone that recognizes one defined epitope on the target antigen — making Monoclonal antibodies uniquely consistent between lots.

Why it matters:

• Monoclonal antibodies offer lot-to-lot reproducibility that is critical for longitudinal studies, quantitative assays, and any experimental design requiring matched performance across timepoints or collaborating labs.
• The defined single-epitope binding profile enables reliable pairing with a non-competing capture antibody for sandwich ELISA, proximity ligation, and flow cytometry multiplex panels.

How to interpret here: A single, well-optimized titration for this Monoclonal antibody transfers reliably across experiments. Confirm whether the target epitope is preserved under your fixation or denaturation conditions before proceeding with IHC or WB applications.

What it means: This antibody was raised in Mouse, producing monoclonal-format IgG produced in mouse hybridomas, offering exceptional lot-to-lot consistency. Anti-mouse secondary antibodies are the most widely catalogued in the industry.

Why it matters:

• The Mouse host species determines which secondary antibody you need for indirect detection — select an anti-Mouse IgG secondary matched to your detection label (HRP, fluorochrome, or biotin).
• In experiments with mouse-origin samples, use anti-mouse secondary antibodies that are pre-adsorbed against mouse IgG, or switch to isotype-specific secondaries to prevent background from endogenous mouse immunoglobulins.

How to interpret here: Confirm availability of an anti-Mouse secondary antibody in your lab before ordering. For multiplex IF, pair this Mouse-raised antibody with antibodies from a different host species to avoid secondary antibody cross-reactivity.

What it means: Unconjugated format means no detection label is attached to this antibody — you supply a compatible secondary antibody or detection reagent of your choice.

Why it matters:

• The Unconjugated format gives maximum flexibility: pair with HRP-, fluorochrome-, or biotin-conjugated secondary antibodies matched to your detection platform, enabling use across WB, IHC, IF, and ELISA without ordering separate conjugated primary formats.
• Signal amplification is possible by using a biotinylated secondary followed by a streptavidin-enzyme conjugate, which is not available with directly conjugated primary antibodies.

How to interpret here: Select an anti-host-species secondary antibody conjugated to your preferred detection label. For most indirect detection workflows, the Unconjugated primary antibody is the recommended starting format.

What it means: YN01156m is the unique clone designation of this monoclonal antibody, identifying the specific hybridoma lineage that defines its epitope and performance characteristics.

Why it matters:

• Clone YN01156m allows precise cross-referencing with published literature — if peer-reviewed studies cite this specific clone, its performance in your assay context is already independently validated.
• Recording clone YN01156m in your methods section enables collaborators and reviewers to replicate your exact reagent, satisfying increasingly stringent journal antibody reporting requirements (RRID registration, clone number disclosure).

How to interpret here: Search clone YN01156m in published literature and antibody validation databases to review independent performance data. Always record the full clone designation in experimental notes for complete reproducibility documentation.

What it means: This antibody has been experimentally validated for 1 application: IHC (Paraffin).

Why it matters:

• IHC (Paraffin)
• Each listed application represents an independently optimized protocol — not a theoretical prediction — giving you confidence that the antibody will perform reliably when used at the recommended conditions for that technique.

How to interpret here: Select the application that matches your assay (IHC (Paraffin)) and refer to the datasheet for the validated dilution range specific to each technique. Using this antibody outside the listed validated applications requires independent optimization and performance verification.