TMEM175 anticorps (AA 278-291)

N° du produit ABIN7581993

Cet anticorps anti-TMEM175 est un anticorps Lapin Polyclonal détectant TMEM175 dans WB et IHC. Adapté pour Souris.

Aperçu rapide pour TMEM175 anticorps (AA 278-291) (ABIN7581993)

Antigène: TMEM175 (Transmembrane Protein 175 (TMEM175))

Reactivité: Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp TMEM175 est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (IHC)

Détail du produit anti-TMEM175 anticorps

Épitope: AA 278-291

Fonction: A Rabbit Polyclonal antibody to TMEM175

Séquence: CEDNVPDPKD VQEK

Specificité: Luminal, 4th loop.

Homologie: Rat - 13 out of 14 amino acid residues identical Human - 12 out of 14 amino acid residues identical

Attributs du produit: Anti-TMEM175 Antibody (ABIN7581993) is a highly specific antibody directed against an epitope of the mouse protein. The antibody can be used in western blot and immunohistochemistry applications. It has been designed to recognize TMEM175 from rat, mouse and human samples.

Purification: Affinity purified on immobilized antigen.

Immunogène: CEDNVPDPKDVQEK, corresponding to amino acid residues 278 - 291 of mouse TMEM175

Isotype: IgG

Information d'application

Indications d'application:

Antigen preadsorption control: 1 μg peptide per 1 μg antibody

Application Dilutions Immunohistochemistry paraffin embedded sections ihc: 1:300

Application Dilutions Western blot wb: 1:200

Restrictions: For Research Use only

Stockage

Format: Lyophilized

Reconstitution: 0.2 mL double distilled water (DDW).

Concentration: 1 mg/mL

Buffer: PBS pH 7.4

Stock: 4 °C,-20 °C

Stockage commentaire:

Storage before reconstitution: The antibody ships as a lyophilized powder at room temperature. Upon arrival, it should be stored at -20°C.

Storage after reconstitution: The reconstituted solution can be stored at 4°C for up to 1 week. For longer periods, small aliquots should be stored at -20°C. Avoid multiple freezing and thawing. Centrifuge all antibody preparations before use (10000 x g 5 min).

Détails sur TMEM175

Antigène: TMEM175 (Transmembrane Protein 175 (TMEM175))

Autre désignation: TMEM175

Sujet: Transmembrane Protein 175, Endosomal/Lysosomal Proton Channel TMEM175,Transmembrane protein 175, TMEM175, is an endosomal/lysosomal proton channel that plays a crucial role in preserving the lysosomal membrane potential and maintaining pH stability. TMEM175 mediates lysosomal proton efflux, known as the "H+ leak" pathway, preventing excessive acidification of lysosomes.1 Intracellular endosomes and lysosomes rely on a vacuolar-type H+ ATPase (V-ATPase) to establish a significant proton concentration gradient across their membranes, which plays a crucial role in facilitating active transport of ions and metabolites between the vesicular lumen and the cytosol. To effectively digest macromolecules, lysosomes rely on an acidic environment with a pH range of 4.5 to 5.0, which is maintained through the entry of protons by the V-ATPase pump and their exit through the "H+ leak" pathway, which is the passive release of H+ into the cytosol. TMEM175 functions as a proton-activated, proton-selective channel on the lysosomal membrane in order to mediate the "H+ leak" pathway, prohibiting the excessive acidification of lysosomes. When lysosomes are acidified beyond the typical range, TMEM175 is activated, prohibiting further lysosomal acidification.1Mammalian TMEM175 consists of two homologous 6-TM domains and is suggested to function as a dimer. TM1 serves as the inner helix lining the pore and forms an hourglass-shaped ion permeation pathway within the channel. The C-terminal half of TM1 contains hydrophobic residues that create a bottleneck along the ion conduction pathway, serving as the selectivity filter of the channel. TMEM175 conducts K+ constitutively at pH 7.4, but shows reduced K+ permeation at lower pH . Conversely, proton current through TMEM175 increases with decreasing pH due to the increased proton gradient. Molecular dynamics simulation, structure-based mutagenesis, and electrophysiological analysis suggest that K+ ions and protons share the same permeation pathway in TMEM175.2,3Altered lysosomal pH disrupts various cellular processes, including lysosomal degradation, cargo loading, catabolite export, vesicle movement, and nutrient sensing. This impairment contributes to the pathogenesis of neurodegenerative diseases such as Parkinson's disease, Alzheimer's disease, and lysosomal storage diseases. Optimization of lysosomal pH can effectively clear toxic protein aggregates associated with these diseases. Thus, maintaining lysosomal pH homeostasis plays a crucial role in lysosome function, cellular health, and neuropathology.1

ID gène: 72392

UniProt: Q9CXY1