
Human LRRN4CL (LRRN4 C-terminal-like protein) ELISA KIT (HUFI05098)
Price on request
| SKU | Price | Quantity |
|---|---|---|
| HUFI05098 | Price on request |
Description
This description has not been verified against the manufacturer's datasheet. Check the datasheet before you order, or ask us to confirm a specification. Ask us to confirm
The LRRN4 C-terminal-like protein (LRRN4CL) is a member of the leucine-rich repeat neuronal protein family, structurally related to LRRN4 and characterized by its C-terminal-like domain architecture. This human protein has been studied in contexts of neuronal development, membrane receptor function, and central nervous system gene expression patterns, with investigators examining its localization in neural tissue and its relationship to transmembrane signaling complexes.
The Assay Genie ELISA kit provides quantitative measurement of human LRRN4CL, supporting neuroscience research, biomarker investigation, and studies of membrane-associated signaling proteins. The microplate-based workflow enables researchers to process multiple samples simultaneously using standard laboratory plate readers, and the included standard curve materials allow interpolation of unknown sample concentrations against a defined reference range.
Each kit is supplied as a microplate format with detection reagents, wash buffer, and substrate solution. Reagents should be kept refrigerated upon arrival; the product shelf life supports typical research timelines when stored as directed. Avoid repeated freeze-thaw cycles and aliquot reagents as needed to preserve enzymatic activity for downstream applications including cell culture supernatant work, tissue lysate analysis, and related in vitro sample preparations.
The assay is intended for research use only and is not validated for diagnostic procedures. Researchers should consult the accompanying product documentation for detailed protocols, expected performance characteristics, and species-specific reactivity information relevant to their experimental design.
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