DMT1 Antibody (YA4629)
(Synonyms: DCT 1 antibody; dct-1 antibody; DCT1 antibody; Divalent cation transporter 1 antibody; Divalent metal transporter 1 antibody; DMT 1 antibody; DMT-1 antibody; DMT1 antibody; FLJ37416 antibody; Natural resistance associated macrophage protein 2 antibody; Natural resistance-associated macrophage protein 2 antibody; NRAM2_HUMAN antibody; NRAMP 2 antibody; NRAMP2 antibody; OK/SW-cl.20 antibody; Slc11a2 antibody; Solute carrier family 11 (proton coupled divalent metal ion transporters) member 2 antibody; Solute carrier family 11 member 2 antibody)Based on 1 Customer Validation
DMT1 Antibody (YA4629) is a Rabbit-derived and non-conjugated IgG monoclonal antibody, targeting to DMT1.
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Host:
Rabbit
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Isotype:
IgG
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Application:
WB, IHC-P, FC
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Reactivity :
Human
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Formulation:
Supplied in PBS (pH7.4), 0.1% BSA, 40% Glycerol. Preservative: 0.05% Sodium Azide.
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Conjugation:
Non-conjugated
Applications
| Application |
WB
WB: Western Blot
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IHC-P
IHC-P: Immunohistochemistry-Paraffin
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FC
FC: Flow Cytometry
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| Dilution Ratio | 1:2000 | 1:1000 | 1:1000 |
Product Details
DMT1 Antibody (YA4629) is a Rabbit-derived and non-conjugated IgG monoclonal antibody, targeting to DMT1.
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Host Rabbit
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Clonality Monoclonal,Recombinant
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Species ReactivityHuman
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Observed Molecular WeightObserved band size: 75 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: 62 kDa
Recombinant protein within human DMT1 aa 1-400.
Affinity Purified
Non-conjugated
Unmodified
IgG
Product Properties
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Appearance
Liquid
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Formulation
Supplied in PBS (pH7.4), 0.1% BSA, 40% Glycerol. Preservative: 0.05% Sodium Azide.
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Concentration
Batch-dependent, Please check the COA for the concentration of each lot. Check Lot Concentration
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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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Western blot analysis of extracts from HEK293 (lane 2(20μg), HepG2 (lane 3(20μg), Hela (lane 4(20μg) using DMT1 (HY-P84933) Rabbit mAb. Proteins were transferred to a PVDF membrane and blocked with 5% non-fat milk in TBST for 2 hour at room temperature. The primary antibody (1/1000) and Loading control antibody (Beta Actin, HY-P80438, 1/10000) was used in 5% non-fat milk in TBST at 4°C overnight. Goat Anti-Mouse/Rabbit IgG-HRP Secondary Antibody (1/10000) was used for 1 hour at room temperature.
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Immunohistochemical analysis of paraffin-embedded human endometrium tissue using DMT1 Antibody (HY-P84933, 1/1000). The section was pretreated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) for 8 minutes. The tissues were blocked with quick block buffer for 0.5 hours at room temperature, washed with PBS and PBST, and then incubated with the primary antibody overnight at 4℃. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.
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Immunohistochemical analysis of paraffin-embedded human epididymis tissue using DMT1 Antibody (HY-P84933, 1/1000). The section was pretreated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) for 8 minutes. The tissues were blocked with quick block buffer for 0.5 hours at room temperature, washed with PBS and PBST, and then incubated with the primary antibody overnight at 4℃. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.
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Immunohistochemical analysis of paraffin-embedded human kidney tissue using DMT1 Antibody (HY-P84933, 1/1000). The section was pretreated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) for 8 minutes. The tissues were blocked with quick block buffer for 0.5 hours at room temperature, washed with PBS and PBST, and then incubated with the primary antibody overnight at 4℃. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.
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Immunohistochemical analysis of paraffin-embedded human prostate tissue using DMT1 Antibody (HY-P84933, 1/1000). The section was pretreated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) for 8 minutes. The tissues were blocked with quick block buffer for 0.5 hours at room temperature, washed with PBS and PBST, and then incubated with the primary antibody overnight at 4℃. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.
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Immunohistochemical analysis of paraffin-embedded human testis tissue using DMT1 Antibody (HY-P84933, 1/1000). The section was pretreated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) for 8 minutes. The tissues were blocked with quick block buffer for 0.5 hours at room temperature, washed with PBS and PBST, and then incubated with the primary antibody overnight at 4℃. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.
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Immunohistochemical analysis of paraffin-embedded human lung tissue using DMT1 Antibody (HY-P84933, 1/1000). The section was pretreated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) for 8 minutes. The tissues were blocked with quick block buffer for 0.5 hours at room temperature, washed with PBS and PBST, and then incubated with the primary antibody overnight at 4℃. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.
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Immunohistochemical analysis of paraffin-embedded human salivary gland tissue using DMT1 Antibody (HY-P84933, 1/1000). The section was pretreated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) for 8 minutes. The tissues were blocked with quick block buffer for 0.5 hours at room temperature, washed with PBS and PBST, and then incubated with the primary antibody overnight at 4℃. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.
Background
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Function
DMT1 is a Proton-coupled metal ion symporter operating with a proton to metal ion stoicH2O2etry of 1:1. Selectively transports various divalent metal cations, in decreasing affinity: Cd(2+) > Fe(2+) > Co(2+), Mn(2+) >> Zn(2+), Ni(2+), VO(2+). Essential for maintenance of iron homeostasis by modulating intestinal absorption of dietary Fe(2+) and TF-associated endosomal Fe(2+) transport in erytH2O2d precursors and other cells. Enables Fe(2+) and Mn(2+) ion entry into mitochondria, and is thus expected to promote mitochondrial heme synthesis, iron-sulfur cluster biogenesis and antioxidant defense. Can mediate uncoupled fluxes of either protons or metal ions[1][2][3][4][5][6].
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Subcellular Localization
Early endosome membrane; Multi-pass membrane protein; Apical cell membrane; Multi-pass membrane protein; Late endosome membrane; Multi-pass membrane protein; Lysosome membrane; Multi-pass membrane protein; Apical cell membrane; Multi-pass membrane protein; Cell membrane; Multi-pass membrane protein; Extracellular vesicle membrane; Multi-pass membrane protein; Cell membrane; Mitochondrion outer membrane; Multi-pass membrane protein; Golgi apparatus, trans-Golgi network membrane; Multi-pass membrane protein; Recycling endosome membrane; Multi-pass membrane protein
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Expression
Tissue_specificity:Ubiquitously expressed. Expressed in erytH2O2d progenitors
Induction:Up-regulated under iron-depletion conditions. Down-regulated in response to high extracellular iron levels; Up-regulated under iron-depletion conditions. Down-regulated in response to high extracellular iron levels; Up-regulated under iron-depletion conditions. Down-regulated in response to high extracellular iron levels -
Isoforms & Post-Translational Modification
P49281 has 5 isomers: P49281-1: 62266 Da (predicted); P49281-2: 61456 Da (predicted); P49281-3: 64704 Da (predicted); P49281-4: 65514 Da (predicted); P49281-5: 61048 Da (predicted).
Ubiquitinated by WWP2;N-glycosylated -
Subunit
Forms a complex with NDFIP1 and NEDD4L, in cortical neurons, in response to iron and cobalt exposure; this interaction leads to SLC11A2 ubiquitination by NEDD4L and proteasome-dependent degradation (PubMed:19706893).
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SwissProt ID
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Synonyms
DCT 1 antibody; dct-1 antibody; DCT1 antibody; Divalent cation transporter 1 antibody; Divalent metal transporter 1 antibody; DMT 1 antibody; DMT-1 antibody; DMT1 antibody; FLJ37416 antibody; Natural resistance associated macrophage protein 2 antibody; Natural resistance-associated macrophage protein 2 antibody; NRAM2_HUMAN antibody; NRAMP 2 antibody; NRAMP2 antibody; OK/SW-cl.20 antibody; Slc11a2 antibody; Solute carrier family 11 (proton coupled divalent metal ion transporters) member 2 antibody; Solute carrier family 11 member 2 antibody
Documentation
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Data Sheet (234 KB)
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SDS (254 KB)
- English - EN (254 KB)
- Français - FR (254 KB)
- Deutsch - DE (254 KB)
- Norwegian - NO (254 KB)
- Español - ES (254 KB)
- Swedish - SV (254 KB)
- Italian - IT (254 KB)
- Korean - KR (254 KB)
- Portuguese - PT (254 KB)
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User Guide for Antibodies (1077 KB)