Signal Transduction Antibodies 1
Anti-DMT1 Antibody (CAB10231)
- SKU:
- CAB10231
- Product Type:
- Antibody
- Reactivity:
- Human
- Reactivity:
- Mouse
- Reactivity:
- Rat
- Host Species:
- Rabbit
- Isotype:
- IgG
- Antibody Type:
- Polyclonal Antibody
- Research Area:
- Signal Transduction
Description
Antibody Name: | Anti-DMT1 Antibody |
Antibody SKU: | CAB10231 |
Antibody Size: | 20uL, 50uL, 100uL |
Application: | WB IHC IF |
Reactivity: | Human, Mouse, Rat |
Host Species: | Rabbit |
Immunogen: | Recombinant fusion protein containing a sequence corresponding to amino acids 1-100 of human DMT1 (NP_000608.1). |
Application: | WB IHC IF |
Recommended Dilution: | WB 1:1000 - 1:2000 IHC 1:50 - 1:200 IF 1:50 - 1:200 |
Reactivity: | Human, Mouse, Rat |
Positive Samples: | 293T, BxPC-3, SH-SY5Y, Rat testis, Rat kidney |
Immunogen: | Recombinant fusion protein containing a sequence corresponding to amino acids 1-100 of human DMT1 (NP_000608.1). |
Purification Method: | Affinity purification |
Storage Buffer: | Store at -20'C. Avoid freeze / thaw cycles. Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3. |
Isotype: | IgG |
Sequence: | MVLG PEQK MSDD SVSG DHGE SASL GNIN PAYS NPSL SQSP GDSE EYFA TYFN EKIS IPEE EYSC FSFR KLWA FTGP GFLM SIAY LDPG NIES DLQS GAVA |
Gene ID: | 4891 |
Uniprot: | P49281 |
Cellular Location: | Cell membrane, Early endosome, Endosome membrane, Mitochondrion outer membrane, Multi-pass membrane protein |
Calculated MW: | 61kDa/62kDa/64kDa/65kDa |
Observed MW: | 72KDa |
Synonyms: | SLC11A2, AHMIO1, DCT1, DMT1, NRAMP2 |
Background: | This gene encodes a member of the solute carrier family 11 protein family. The product of this gene transports divalent metals and is involved in iron absorption. Mutations in this gene are associated with hypochromic microcytic anemia with iron overload. A related solute carrier family 11 protein gene is located on chromosome 2. Multiple transcript variants encoding different isoforms have been found for this gene. |
UniProt Protein Function: | SLC11A2: Important in metal transport, in particular iron. Can also transport manganese, cobalt, cadmium, nickel, vanadium and lead. Involved in apical iron uptake into duodenal enterocytes. Involved in iron transport from acidified endosomes into the cytoplasm of erythroid precursor cells. May play an important role in hepatic iron accumulation and tissue iron distribution. Defects in SLC11A2 are a cause of hypochromic microcytic anemia (HCMA). The disease is characterized by an abnormal hemoglobin content in the erythrocytes which are reduced in size. It may be hereditary or acquired. Mutations in SLC11A2 are associated with progressive liver iron overload and normal to moderately elevated serum ferritin levels. Belongs to the NRAMP family. 4 isoforms of the human protein are produced by alternative splicing. |
UniProt Protein Details: | Protein type:Transporter; Transporter, SLC family; Membrane protein, multi-pass; Membrane protein, integral Chromosomal Location of Human Ortholog: 12q13 Cellular Component: apical part of cell; apical plasma membrane; brush border membrane; cytoplasm; cytoplasmic vesicle; early endosome; integral to plasma membrane; late endosome membrane; lysosomal membrane; membrane; nucleus; perinuclear region of cytoplasm; plasma membrane; recycling endosome; vacuole Molecular Function:cadmium ion binding; cadmium ion transmembrane transporter activity; copper ion transmembrane transporter activity; ferrous iron transmembrane transporter activity; ferrous iron uptake transmembrane transporter activity; iron ion transmembrane transporter activity; lead ion transmembrane transporter activity; manganese ion transmembrane transporter activity; protein binding; solute:hydrogen symporter activity; transition metal ion transmembrane transporter activity Biological Process: cellular iron ion homeostasis; copper ion transport; ferrous iron transport; lead ion transport; manganese ion transport; response to iron ion Disease: Anemia, Hypochromic Microcytic, With Iron Overload 1 |
NCBI Summary: | This gene encodes a member of the solute carrier family 11 protein family. The product of this gene transports divalent metals and is involved in iron absorption. Mutations in this gene are associated with hypochromic microcytic anemia with iron overload. A related solute carrier family 11 protein gene is located on chromosome 2. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Apr 2010] |
UniProt Code: | P49281 |
NCBI GenInfo Identifier: | 8247934 |
NCBI Gene ID: | 4891 |
NCBI Accession: | P49281.2 |
UniProt Secondary Accession: | P49281,O43288, O60932, O94801, Q498Z5, Q8IUD7, Q96J35 B3KT08, B4DK84, F5H741, |
UniProt Related Accession: | P49281 |
Molecular Weight: | 61,048 Da |
NCBI Full Name: | Natural resistance-associated macrophage protein 2 |
NCBI Synonym Full Names: | solute carrier family 11 member 2 |
NCBI Official Symbol: | SLC11A2 |
NCBI Official Synonym Symbols: | DCT1; DMT1; AHMIO1; NRAMP2 |
NCBI Protein Information: | natural resistance-associated macrophage protein 2 |
UniProt Protein Name: | Natural resistance-associated macrophage protein 2 |
UniProt Synonym Protein Names: | Divalent cation transporter 1; Divalent metal transporter 1; DMT-1; Solute carrier family 11 member 2 |
Protein Family: | Natural resistance-associated macrophage protein |
UniProt Gene Name: | SLC11A2 |
UniProt Entry Name: | NRAM2_HUMAN |