TRPM7 antibody (AA 756-855)

Catalog No. ABIN6149588

Product Details anti-TRPM7 Antibody

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

Binding Specificity: AA 756-855

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This TRPM7 antibody is un-conjugated

Application: Western Blotting (WB)

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

Cross-Reactivity: Mouse

Characteristics: Polyclonal Antibodies

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

Isotype: IgG

Application Details

Application Notes: WB,1:500 - 1:2000

Restrictions: For Research Use only

Handling

Format: Liquid

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

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: -20 °C

Storage Comment: Store at -20°C. Avoid freeze / thaw cycles.

Target Details for TRPM7

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

Alternative Name: TRPM7 (TRPM7 Products)

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

Background: 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

Molecular Weight: 212 kDa

Gene ID: 54822

UniProt: Q96QT4