GTX54865
TRPM7 antibody
Cannot supply to this region.
- SKU:
- GTX54865
- Additional Names:
- transient receptor potential cation channel subfamily M member 7 , ALSPDC , CHAK , CHAK1 , LTRPC7 , LTrpC-7 , TRP-PLIK
- Application:
- WB, IHC-P, IF, ICC
- Concentration:
- 0.8 mg/ml
- Physical State:
- Liquid
- Species Reactivity:
- Human
- Purification:
- Affinity Purified
- Storage Conditions:
- -20[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., 2-8[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., -20[o]C/-70[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted.
- Supplier:
- Genetex
- Host:
- Rabbit
- Reactivities:
- Human, Mouse, Rat
- Buffer:
- PBS, 1% BSA, 0.05% Sodium azide.
- Immunogen:
- Peptide CKRRKKDKTSDGPKLFLTEE, corresponding to amino acid residues 1146-1165 (Intracellular, C-terminus) of human TRPM7 (Accession : Q96QT4).
- Uniprot:
- Q96QT4
- Synonyms:
- ALSPDC;CHAK;CHAK1;channel-kinase 1;long transient receptor potential channel 7;LTRPC ion channel family member 7;LTrpC-7;LTRPC7;transient receptor potential cation channel subfamily M member 7;transient receptor potential-phospholipase C-interacting kinase;TRP-PLIK
- Extra Details:
- This gene belongs to the melastatin subfamily of transient receptor potential family of ion channels. 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. The encoded protein is involved in cytoskeletal organization, cell adhesion, cell migration and organogenesis. Defects in this gene are a cause of amyotrophic lateral sclerosis-parkinsonism/dementia complex of Guam. The gene may also be associated with defects of cardiac function. [provided by RefSeq, Aug 2017]
- Shipping Conditions:
- Blue Ice