TRPM7 Antibody (YA2391)(PBS only)
(Synonyms: ALSPDC; CHAK; CHAK1; LTrpC7; TRPM7)TRPM7 Antibody (YA2391) is a Rabbit-derived and non-conjugated IgG monoclonal antibody, targeting to TRPM7.
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Host:
Rabbit
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Isotype:
IgG
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Application:
WB, ICC/IF, FC
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Reactivity :
Human, Mouse, Rat
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Formulation:
Supplied in PBS, pH 7.4.
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Conjugation:
Non-conjugated
Applications
| Application |
WB
WB: Western Blot
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ICC/IF
ICC/IF: Immunocytochemistry/
Immunofluorescence |
FC
FC: Flow Cytometry
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|---|---|---|---|
| Dilution Ratio | 1:500-1:1000 | 1:50-1:200 | 1:50-1:100 |
Product Details
TRPM7 Antibody (YA2391) is a Rabbit-derived and non-conjugated IgG monoclonal antibody, targeting to TRPM7.
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Host Rabbit
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Species ReactivityHuman, Mouse, Rat
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Observed Molecular WeightObserved band size: 213 kDaNote: Due to possible protein modifications or aggregation, the molecular weight should be confirmed by actual measurement, and the predicted value is for reference only.
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Calculated Molecular Weight Predicted band size: 213 kDa
A synthesized peptide derived from human TRPM7
Affinity Chromatography
Non-conjugated
IgG
Product Properties
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Appearance
Solution
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Formulation
Supplied in PBS, pH 7.4.
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Storage & Stability
Stored at -20°C for 1 year. Avoid repeated freeze / thaw cycles.
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Shipping
Shipping with blue ice.
Verification Images
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Immunocytochemistry analysis of SH-SY5Y cells labeling TRPM7 with TRPM7 antibody (HY-P82646) at 1/50 dilution. Cells were fixed in 4% paraformaldehyde for 15 minutes at room temperature, permeabilized with 0.1% Triton X-100 for 10 minutes at room temperature, then blocked with QuickBlock™ Blocking Buffer for Immunol Staining for 10 min at room temperature. Cells were then incubated with TRPM7 antibody (HY-P82646) at 1/50 dilution in QuickBlock™ Blocking Buffer for Immunol Staining at 4 ℃. Alexa Fluor® 488-conjugated AffiniPure Goat Anti-Rabbit IgG H&L(HY-P8002, Green) was used as the secondary antibody at 1/1,000 dilution. PBS instead of the primary antibody was used as the secondary antibody only control. The Nuclear counterstain was DAPI (Blue).
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Immunocytochemistry analysis of SH-SY5Y cells labeling TRPM7 with TRPM7 antibody (HY-P82646) at 1/100 dilution. Cells were fixed in 4% paraformaldehyde for 15 minutes at room temperature, permeabilized with 0.1% Triton X-100 for 10 minutes at room temperature, then blocked with QuickBlock™ Blocking Buffer for Immunol Staining for 10 min at room temperature. Cells were then incubated with TRPM7 antibody (HY-P82646) at 1/100 dilution in QuickBlock™ Blocking Buffer for Immunol Staining at 4 ℃. Alexa Fluor® 488-conjugated AffiniPure Goat Anti-Rabbit IgG H&L(HY-P8002, Green) was used as the secondary antibody at 1/1,000 dilution. PBS instead of the primary antibody was used as the secondary antibody only control. The Nuclear counterstain was DAPI (Blue).
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Flow cytometric analysis of 1X10^6 Hela cells labeling TRPM7 Antibody (YA2391) (HY-P82646, red). Cells were fixed with 4% paraformaldehyde. Then stained with the primary antibody at 1/50 dilution for an hour at 4℃. Alexa Fluor® 488-conjugated AffiniPure Goat Anti-Rabbit IgG H&L (HY-P8002) was used as the secondary antibody at 1/1,000 dilution for 30 minutes at 4℃. Rabbit IgG Isotype Control (HY-P80879, blue) was used as the isotype control, cells without incubation with primary antibody were used as the unlabeled control (black).
Background
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Function
TRPM7 is a TRP melastatin channel-kinase that conducts divalent and monovalent cations and combines channel and enzymatic activities[1]. Mechanistically, vascular TRPM7 supports Mg2+ homeostasis and regulates vascular smooth muscle cell growth, apoptosis, adhesion, contraction, cytoskeletal organization, and migration[2]. In inflammation, TRPM7 channel and kinase activity regulate neutrophil transmigration and reactive oxygen species production through Akt/mTOR signaling[3]. In intestinal disease models, TRPM7 knockdown reduces LPS-induced apoptosis and inflammatory cytokine expression by modulating TLR4/NF-κB and MEK/ERK pathways[4]. In kidney fibrosis models, TRPM7 expression increases after unilateral ureteral obstruction, while the inhibitor NS8593 reduces tubular and interstitial cell proliferation and TGF-β1/Smad signaling[5]. Compared with related TRPM6, which is found primarily in epithelial cells, TRPM7 is ubiquitously expressed, making it a broader experimental target for ion-homeostasis and disease-mechanism studies[2]. For pharmacological research, carvacrol inhibits TRPM7 current and reduces neonatal hypoxic-ischemic brain injury, whereas CBGA suppresses TRPM7 currents through a kinase-domain-dependent mechanism[6][7].
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Subcellular Localization
Cell membrane; Multi-pass membrane protein; Cytoplasmic vesicle membrane; Multi-pass membrane protein; Nucleus
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Subunit
Homotetramer (By similarity). Forms heteromers with TRPM6; heteromeric channels are functionally different from the homomeric channels (PubMed:14976260, PubMed:16636202)
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SwissProt ID
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Synonyms
ALSPDC; CHAK; CHAK1; LTrpC7; TRPM7
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Research Field
Neuroscience
Documentation
References
[2]. Yogi A, et al. Transient receptor potential melastatin 7 (TRPM7) cation channels, magnesium and the vascular system in hypertension. Circ J. 2011;75(2):237-45. [Content Brief]
[3]. Nadolni W, et al. TRPM7 Kinase Is Essential for Neutrophil Recruitment and Function via Regulation of Akt/mTOR Signaling. Front Immunol. 2021 Feb 15;11:606893. [Content Brief]
[4]. An L, et al. Knockdown of TRPM7 attenuates apoptosis and inflammation in neonatal necrotizing enterocolitis model cell IEC-6 via modulating TLR4/NF-κB and MEK/ERK pathways. Iran J Basic Med Sci. 2022 Aug;25(8):947-953. [Content Brief]
[5]. Suzuki S, et al. TRPM7 contributes to progressive nephropathy. Sci Rep. 2020 Feb 11;10(1):2333. [Content Brief]
[6]. Chen W, et al. TRPM7 inhibitor carvacrol protects brain from neonatal hypoxic-ischemic injury. Mol Brain. 2015 Feb 19;8:11. [Content Brief]
[7]. Suzuki S, et al. Cannabigerolic Acid (CBGA) Inhibits the TRPM7 Ion Channel Through its Kinase Domain. Function (Oxf). 2023 Dec 7;5(1):zqad069. [Content Brief]