Anti-TRPM7 antibody (Extracellular region) [M573] (STJA0005616)

SPECIFICATIONS
ClonalityMonoclonal
HostMouse
ConjugationUnconjugated
IsotypeIgG1
ImmunogenClone M573 was generated from TRPM7 synthetic peptide (coupled to carrier) corresponding to amino acids in the extracellular region of human TRPM7. This site is well conserved in rat and mouse TRPM7, but has low homology to other TRPM family members.
STJA0005616-100
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General Information

Short DescriptionMouse monoclonal antibody anti-TRPM7 (Extracellular region) is suitable for use in Western Blot research applications.
ApplicationsWB
HostMouse
ReactivityHuman/Mouse/Rat
NoteSTRICTLY FOR FURTHER SCIENTIFIC RESEARCH USE ONLY (RUO). MUST NOT TO BE USED IN DIAGNOSTIC OR THERAPEUTIC APPLICATIONS.

Product Properties

ClonalityMonoclonal
Clone IDM573
IsotypeIgG1
ConjugationUnconjugated
PurificationAntigen Affinity Purified
Dilution RangeWB 1:500
FormulationPBS + 1 mg/ml BSA, 0.05% NaN3 and 50% glycerol
Storage InstructionStore at-20ยฐC for up to 1 year from the date of receipt, and avoid repeat freeze-thaw cycles.

Target Information

Gene SymbolTRPM7
Gene ID54822
Uniprot IDTRPM7_HUMAN
ImmunogenClone M573 was generated from TRPM7 synthetic peptide (coupled to carrier) corresponding to amino acids in the extracellular region of human TRPM7. This site is well conserved in rat and mouse TRPM7, but has low homology to other TRPM family members.
Immunogen RegionExtracellular region
SpecificityThis antibody detects a 220 kDa* protein on SDS-PAGE immunoblots of human MCF7 cells.

Additional Info

Function Bifunctional protein that combines an ion channel with an intrinsic kinase domain, enabling it to modulate cellular functions either by conducting ions through the pore or by phosphorylating downstream proteins via its kinase domain. The channel is highly permeable to divalent cations, specifically calcium (Ca2+), magnesium (Mg2+) and zinc (Zn2+) and mediates their influx. Controls a wide range of biological processes such as Ca2(+), Mg(2+) and Zn(2+) homeostasis, vesicular Zn(2+) release channel and intracellular Ca(2+) signaling, embryonic development, immune responses, cell motility, proliferation and differentiation. The C-terminal alpha-kinase domain autophosphorylates cytoplasmic residues of TRPM7. In vivo, TRPM7 phosphorylates SMAD2, suggesting that TRPM7 kinase may play a role in activating SMAD signaling pathways. In vitro, TRPM7 kinase phosphorylates ANXA1 (annexin A1), myosin II isoforms and a variety of proteins with diverse cellular functions. TRPM7 channel, cleaved form: The cleaved channel exhibits substantially higher current and potentiates Fas receptor signaling. TRPM7 kinase, cleaved form: The C-terminal kinase domain can be cleaved from the channel segment in a cell-type-specific fashion. In immune cells, the TRPM7 kinase domain is clipped from the channel domain by caspases in response to Fas-receptor stimulation. The cleaved kinase fragments can translocate to the nucleus, and bind chromatin-remodeling complex proteins in a Zn(2+)-dependent manner to ultimately phosphorylate specific Ser/Thr residues of histones known to be functionally important for cell differentiation and embryonic development.
Protein Name Transient Receptor Potential Cation Channel Subfamily M Member 7
Channel-Kinase 1
Long Transient Receptor Potential Channel 7
Ltrpc-7
Ltrpc7 Cleaved Into - Trpm7 Kinase - Cleaved Form
M7ck - Trpm7 Channel - Cleaved Form
Database Links Reactome: R-HSA-3295583
Cellular Localisation Cell Membrane
Multi-Pass Membrane Protein
Cytoplasmic Vesicle Membrane
Localized Largely In Intracellular Zn(2+)-Storage Vesicles
Trpm7 Kinase
Cleaved Form: Nucleus
Alternative Antibody Names Anti-Transient Receptor Potential Cation Channel Subfamily M Member 7 antibody
Anti-Channel-Kinase 1 antibody
Anti-Long Transient Receptor Potential Channel 7 antibody
Anti-Ltrpc-7 antibody
Anti-Ltrpc7 Cleaved Into - Trpm7 Kinase - Cleaved Form antibody
Anti-M7ck - Trpm7 Channel - Cleaved Form antibody
Anti-TRPM7 antibody
Anti-CHAK1 antibody
Anti-LTRPC7 antibody

Information sourced from Uniprot.org

Citations

Product Review