TMEM111 Antibody [B9P11]

Catalog No.: F5124

    Application: Reactivity:

    当該製品は品切れ状态で、ごメールアドレスを教えていただければ、在庫があると、メールで顧客様に伝えます。

    代表番号: 045-509-1970|電子メール:sales@selleck.co.jp

    使用情報

    Dilution
    1:2000-1:10000
    1:250-1:1000
    1:200-1:800
    Application
    WB, IHC, IF
    Source
    Mouse Monoclonal Antibody
    Reactivity
    Human, Mouse, Rat, Pig
    Storage Buffer
    PBS, pH 7.2+50% Glycerol+0.05% BSA+0.01% NaN3
    Storage (from the date of receipt)
    -20°C (avoid freeze-thaw cycles), 2 years
    Predicted MW Observed MW
    30 kDa 30 kDa
    *なぜ予測分子量と実際の分子量が異なるのか?
    下記の原因により、実際の分子量が予測と異なる:タンパク質の翻訳後修飾(リン酸化/糖鎖付加),スプライシングバリアント,イソフォーム,相対的な電荷,ポリマー。

    Datasheet & SDS

    生物学的記述

    Specificity
    TMEM111 Antibody [B9P11] detects endogenous levels of total TMEM111 protein.
    Clone
    B9P11
    Synonym(s)
    ER membrane protein complex subunit 3; Transmembrane protein 111; EMC3; TMEM111
    Background
    TMEM111, or Transmembrane Protein 111, is an integral endoplasmic reticulum membrane protein of about 26 kilodaltons and is part of the TMEM family of poorly characterized multi-spanning membrane proteins that help regulate protein quality control and cellular homeostasis in tissues such as the brain, liver, and kidney. TMEM111 is a small, hydrophobic protein with multiple predicted transmembrane domains that form an intramembrane scaffold, and it has cytoplasmic loops that interact with ER-associated degradation machinery and the Bag3 chaperone complex, though its specific motifs and residues are not well-defined due to limited structural data. Its main function is to coordinate the ubiquitin-proteasome and ER-associated degradation pathways by tethering misfolded proteins to degradation complexes, facilitating their ubiquitination through E2 conjugases, and preventing toxic protein aggregation during ER stress, thus maintaining proteostasis and cell viability. TMEM111 also supports the Bag3-HSP70-HSC70 chaperone network to selectively degrade aggregation-prone proteins, connects ER stress responses to autophagy, and ensures proper protein turnover through lysosomal and proteasomal routes. When TMEM111 is dysfunctional, ER-associated degradation becomes less efficient, leading to protein accumulation implicated in diseases such as Alzheimer's, due to amyloid processing defects, and liver disorders from impaired hepatocyte homeostasis.
    References

    技術サポート

    ストックの作り方、阻害剤の保管方法、細胞実験や動物実験の際に注意すべき点など、製品を取扱う時に問い合わせが多かった質問に対しては取扱説明書でお答えしています。

    Handling Instructions

    他に質問がある場合は、お気軽にお問い合わせください。

    * 必須

    大学・企業名を記入してください
    名前を記入してください
    電子メール・アドレスを記入してください 有効なメールアドレスを入力してください
    お問い合わせ内容をご入力ください