| Field | Specification |
|---|---|
| Mfr No | |
| Accession Number | |
| Alternative Names | MAP1LC3C; LC3C; LC3-like protein 2; MAP1 light chain 3-like protein 2 |
| Assay Time | |
| Assay Type | |
| Detection Method | |
| Gene ID | |
| Product Type | |
| Reactivity | |
| Sample Type(s) | Cell culture supernatants, Serum, Plasma, Other biological fluids |
| Shipping | |
| Storage |
Features & Benefits
Human Microtubule-associated proteins 1A/1B light chain 3C (MAP1LC3C) ELISA Kit has high sensitivity and excellent specificity for detection of Human MAP1LC3C. No significant cross-reactivity or interference between Human MAP1LC3C and analogues was observed.
Background
Autophagy is a highly regulated bulk degradation process that plays an important role in cellular maintenance and development. MAP1LC3C is 1 of 3 orthologs of the yeast autophagosome protein Atg8. The deduced 147-amino acid protein shares 55% identity with rat Map1lc3. Northern blot analysis detected a 1.9-kb transcript expressed predominantly in placenta, lung, and ovary, with little to no expression in other tissues examined. Western blot analysis of transfected human embryonic kidney cells detected MAP1LC3C proteins of about 16 and 15.5 kD.
MAP1LC3C underwent C-terminal cleavage after the conserved residue gly120. Gly120 was required for posttranslational modification of the MAP1LC3C protein.
This Microtubule-associated proteins 1A/1B light chain 3C (MAP1LC3C) ELISA kit is validated for use with Cell culture supernatants, Serum, Plasma, Other biological fluids. Samples should be collected, processed, and stored correctly to preserve analyte integrity — avoid repeated freeze-thaw cycles and centrifuge to remove particulates before use. Dilute samples exceeding the kit's detection range using the supplied assay diluent. Hemolytic, icteric, or lipemic samples may affect assay performance and should be tested with caution.
This is a sandwich ELISA kit employing an HRP (horseradish peroxidase)-conjugated secondary antibody paired with a TMB (3,3′,5,5′-tetramethylbenzidine) colorimetric substrate. In the sandwich format, the target analyte Microtubule-associated proteins 1A/1B light chain 3C (MAP1LC3C) captured on the microplate surface is detected by the conjugated antibody, generating a colorimetric signal proportional to analyte concentration. The reaction is stopped and absorbance measured at 450 nm on a standard microplate reader.
The complete protocol, from sample addition to final plate reading, requires approximately 3–5 hours. This includes two incubation periods (analyte binding and detection antibody steps), intermediate wash cycles to remove unbound material, 15–30 minutes of TMB substrate development, and final stop-solution addition before absorbance reading. Exact timing will vary with experience level and the number of samples processed in parallel.
Required equipment: (1) a microplate spectrophotometer capable of reading absorbance at 450 nm (reference wavelength 540–570 nm recommended for background correction); (2) precision single-channel or multichannel pipettes; (3) a plate washer or multichannel aspirator; (4) a microcentrifuge for sample clarification; and (5) a 37°C incubator or stable room-temperature environment. No fluorescence or luminescence reader is required — standard colorimetric plate readers are fully compatible with this kit.
This ELISA kit is formally validated for Human. Cross-reactivity with species not listed in the specification has not been independently characterized. Variability in protein sequence homology across species means that performance in unlisted species cannot be guaranteed without additional validation. For cross-species detection requirements or non-standard sample matrices, please contact BioHippo support or refer to the manufacturer's technical team for guidance.
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