TRPM7 anticorps (AA 756-855)

N° du produit ABIN6149588

Détail du produit anti-TRPM7 anticorps

Antigène: TRPM7 (Transient Receptor Potential Cation Channel, Subfamily M, Member 7 (TRPM7))

Épitope: AA 756-855

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp TRPM7 est non-conjugé

Application: Western Blotting (WB)

Séquence: NSWYKVILSI LVPPAILLLE YKTKAEMSHI PQSQDAHQMT MDDSENNFQN ITEEIPMEVF KEVRILDSNE GKNEMEIQMK SKKLPITRKF YAFYHAPIVK

Réactivité croisée: Souris

Attributs du produit: Polyclonal Antibodies

Immunogène: Recombinant fusion protein containing a sequence corresponding to amino acids 756-855 of human TRPM7 (NP_060142.3).

Isotype: IgG

Information d'application

Indications d'application: WB,1:500 - 1:2000

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: Store at -20°C. Avoid freeze / thaw cycles.

Détails sur TRPM7

Antigène: TRPM7 (Transient Receptor Potential Cation Channel, Subfamily M, Member 7 (TRPM7))

Autre désignation: TRPM7 (TRPM7 Produits)

Synonymes: anticorps cb495, anticorps TRPM7, anticorps chak, anticorps chak1, anticorps ltrpc7, anticorps trp-plik, anticorps ALSPDC, anticorps CHAK, anticorps CHAK1, anticorps LTRPC7, anticorps TRP-PLIK, anticorps 2310022G15Rik, anticorps 4833414K03Rik, anticorps 5033407O22Rik, anticorps LTrpC-7, anticorps Ltpr7, anticorps Ltrpc7, anticorps TRPPLIK, anticorps Chak, anticorps Trp-plik, anticorps transient receptor potential cation channel subfamily M member 7, anticorps transient receptor potential cation channel, subfamily M, member 7, anticorps TRPM7, anticorps trpm7, anticorps Trpm7

Sujet: The protein encoded by this gene is both an ion channel and a serine/threonine protein kinase. The kinase activity is essential for the ion channel function, which serves to increase intracellular calcium levels and to help regulate magnesium ion homeostasis. Defects in this gene are a cause of amyotrophic lateral sclerosis-parkinsonism/dementia complex of Guam. Alternative splicing of this gene results in multiple transcript variants.,TRPM7,ALSPDC,CHAK,CHAK1,LTRPC7,LTrpC-7,TRP-PLIK,Signal Transduction,Kinase,Neuroscience,Neurodegenerative Diseases,Dopamine Signaling in Parkinson's Disease,Other Neurological disorders,Amyotrophic lateral sclerosis-ALS,TRPM7

Poids moléculaire: 212 kDa

ID gène: 54822

UniProt: Q96QT4