Cat. No. 506 017 |
100 µg purified IgG, lyophilized. Albumin and azide were added for stabilization. For reconstitution add 100 µl H2O to get a 1mg/ml solution in PBS. Then aliquot and store at -20°C to -80°C until use. Antibodies should be stored at +4°C when still lyophilized. Do not freeze! |
Applications |
Immunoprecipitation (IP); Immunoisolation or pulldown of a target molecule using an antibody. For details and product specific hints, please refer to the ”Remarks” section.', $event)" style="cursor: help;">IP: not tested yet Immunocytochemistry (ICC) on 4% PFA fixed cells. Immunoreactivity is usually revealed by fluorescence. Some antibodies require special fixation methods. For details, please refer to the “Remarks” section.', $event)" style="cursor: help;">ICC: not tested yet Immunohistochemistry (IHC) on 4% PFA perfusion fixed tissue with 24h PFA post fixation. Immunoreactivity is usually revealed by fluorescence or a chromogenic substrate. Some antibodies require special fixation methods or antigen retrieval steps. For details, please refer to the ”Remarks” section.', $event)" style="cursor: help;">IHC: not tested yet Immunohistochemistry (IHC-P) of formalin fixed, paraffin embedded (FFPE) tissue (some antibodies require special antigen retrieval steps, please refer to the ”Remarks” section). Immunoreactivity is usually revealed by fluorescence or a chromogenic substrate.', $event)" style="cursor: help;">IHC-P: 1 : 1:1000 up to 1 : 1:2000 (see remarks) |
Clone | SY-118C4 |
Subtype | IgG2a (κ light chain) |
Immunogen | Synthetic peptide corresponding to AA 239 to 252 from human TMEM106B (UniProt Id: Q9NUM4) |
Epitop |
AA 239 to 252 from human TMEM106B (UniProt Id: Q9NUM4) |
Reactivity |
Reacts with: human (Q9NUM4), mouse (Q80X71). Other species not tested yet. |
Specificity | K.O. validated |
Remarks |
WB: This antibody shows an additional unspecific band at 70kD. |
Data sheet | 506_017.pdf |
TMEM106B or Transmembrane protein 106B is a lysosomal type II transmembrane protein which has been identified by a genome-wide association study as a potential risk factor for a neurodegenerative disorder called frontotemporal lobar degeneration (FTLD)(1). The C-terminal luminal domain of TMEM106B undergoes a proteolytic cleavage that forms sarkosyl-insoluble amyloid-like fibrils (residues 120-254) in human brains (2). TMEM106B is ubiquitously expressed, but the function of TMEM106B is almost unknown. TMEM106B is a receptor mediating ACE2-independent SARS-CoV-2 cell entry (3).