TMEM161A antibodies are generated using immunogens such as recombinant protein fragments (e.g., residues 29–98 or 1–100 in humans) . Validations include:
Western Blot: Detects bands at ~45–56 kDa in human, mouse, and rat tissues (e.g., liver, brain) .
IHC: Staining observed in human brain, endometrial cancer, and mouse tissues .
Immunofluorescence: Localizes TMEM161A to the cell membrane in cancer cell lines .
| Application | Dilution Range |
|---|---|
| Western Blot | 1:500–1:2000 |
| IHC (Paraffin) | 1:50–1:500 |
| Immunofluorescence | 1:50–1:200 |
Overexpression of TMEM161A reduces oxidant-induced DNA damage and apoptosis .
Knockdown experiments in osteoblasts (Tmem161a-deficient MC3T3-e1 cells) increased differentiation markers (Alp, Osx), suggesting TMEM161A suppresses osteoblast differentiation .
TMEM161A is overexpressed in non-small cell lung cancer (NSCLC) and linked to MYC-driven oncogenic pathways .
In NSCLC, TMEM161A-specific T cells cross-react with Epstein-Barr virus and E. coli antigens, implicating it in tumor immune evasion .
Tmem161a knockout mice exhibit increased bone mass and strength, indicating its role in inhibiting osteoblast differentiation .
Storage: Stable at -20°C in PBS with 0.02% sodium azide and 50% glycerol .
Antigen Retrieval: For IHC, citrate buffer (pH 6.0) or TE buffer (pH 9.0) is recommended .
Cross-Reactivity: Some antibodies show reactivity with cow, horse, and dog samples .
TMEM161A’s dual role in apoptosis regulation and cancer progression highlights its therapeutic potential. For example: