Cell Biology Antibodies 6
Anti-ANT1/ANT2/ANT3/ANT4 Antibody (CAB15988)
- SKU:
- CAB15988
- Product Type:
- Antibody
- Reactivity:
- Human
- Reactivity:
- Mouse
- Reactivity:
- Rat
- Host Species:
- Rabbit
- Isotype:
- IgG
- Antibody Type:
- Polyclonal Antibody
- Research Area:
- Cell Biology
Description
Antibody Name: | Anti-ANT1/ANT2/ANT3/ANT4 Antibody |
Antibody SKU: | CAB15988 |
Antibody Size: | 20uL, 50uL, 100uL |
Application: | WB IHC |
Reactivity: | Human, Mouse, Rat |
Host Species: | Rabbit |
Immunogen: | A synthetic peptide corresponding to a sequence within amino acids 200 to the C-terminus of human ANT1 (NP_001142.2). |
Application: | WB IHC |
Recommended Dilution: | WB 1:500 - 1:2000 IHC 1:50 - 1:200 |
Reactivity: | Human, Mouse, Rat |
Positive Samples: | Mouse brain, Mouse skeletal muscle, Rat heart |
Immunogen: | A synthetic peptide corresponding to a sequence within amino acids 200 to the C-terminus of human ANT1 (NP_001142.2). |
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: | GMLP DPKN VHIF VSWM IAQS VTAV AGLV SYPF DTVR RRMM MQSG RKGA DIMY TGTV DCWR KIAK DEGA KAFF KGAW SNVL RGMG GAFV LVLY DEIK KYV |
Gene ID: | 291/292/293/83447 |
Uniprot: | P12235/P05141/P12236/Q9H0C2 |
Cellular Location: | |
Calculated MW: | 33kDa/32kDa/35kDa |
Observed MW: | 30kDa |
Synonyms: | ANT1/ANT2/ANT3/ANT4 |
Background: |
UniProt Protein Function: | SLC25A4: Catalyzes the exchange of cytoplasmic ADP with mitochondrial ATP across the mitochondrial inner membrane. Defects in SLC25A4 are a cause of progressive external ophthalmoplegia with mitochondrial DNA deletions autosomal dominant type 2 (PEOA2). Progressive external ophthalmoplegia is characterized by progressive weakness of ocular muscles and levator muscle of the upper eyelid. In a minority of cases, it is associated with skeletal myopathy, which predominantly involves axial or proximal muscles and which causes abnormal fatigability and even permanent muscle weakness. Ragged- red fibers and atrophy are found on muscle biopsy. A large proportion of chronic ophthalmoplegias are associated with other symptoms, leading to a multisystemic pattern of this disease. Additional symptoms are variable, and may include cataracts, hearing loss, sensory axonal neuropathy, ataxia, depression, hypogonadism, and parkinsonism. Belongs to the mitochondrial carrier family. |
UniProt Protein Details: | Protein type:Membrane protein, multi-pass; Membrane protein, integral; Transporter; Transporter, SLC family; Mitochondrial Chromosomal Location of Human Ortholog: 4q35 Cellular Component: mitochondrion; integral to plasma membrane; mitochondrial inner membrane; nucleus Molecular Function:protein binding; adenine transmembrane transporter activity Biological Process: adenine transport; mitochondrial genome maintenance; apoptotic mitochondrial changes; generation of precursor metabolites and energy; viral reproduction; transport; energy reserve metabolic process; regulation of insulin secretion; transmembrane transport Disease: Mitochondrial Dna Depletion Syndrome 12 (cardiomyopathic Type); Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant, 2 |
NCBI Summary: | This gene is a member of the mitochondrial carrier subfamily of solute carrier protein genes. The product of this gene functions as a gated pore that translocates ADP from the cytoplasm into the mitochondrial matrix and ATP from the mitochondrial matrix into the cytoplasm. The protein forms a homodimer embedded in the inner mitochondria membrane. Mutations in this gene have been shown to result in autosomal dominant progressive external opthalmoplegia and familial hypertrophic cardiomyopathy. [provided by RefSeq, Jun 2013] |
UniProt Code: | P12235 |
NCBI GenInfo Identifier: | 113455 |
NCBI Gene ID: | 291 |
NCBI Accession: | P12235.4 |
UniProt Secondary Accession: | P12235,D3DP59, |
UniProt Related Accession: | P12235 |
Molecular Weight: | 298 |
NCBI Full Name: | ADP/ATP translocase 1 |
NCBI Synonym Full Names: | solute carrier family 25 (mitochondrial carrier; adenine nucleotide translocator), member 4 |
NCBI Official Symbol: | SLC25A4 |
NCBI Official Synonym Symbols: | 1; T1; ANT; AAC1; ANT1; PEO2; PEO3; ANT 1; MTDPS12 |
NCBI Protein Information: | ADP/ATP translocase 1; ADP,ATP carrier protein 1; solute carrier family 25 member 4; heart/skeletal muscle ATP/ADP translocator; ADP,ATP carrier protein, heart/skeletal muscle; adenine nucleotide translocator 1 (skeletal muscle) |
UniProt Protein Name: | ADP/ATP translocase 1 |
UniProt Synonym Protein Names: | ADP,ATP carrier protein 1; ADP,ATP carrier protein, heart/skeletal muscle isoform T1; Adenine nucleotide translocator 1; ANT 1; Solute carrier family 25 member 4 |
Protein Family: | ADP/ATP translocase |
UniProt Gene Name: | SLC25A4 |
UniProt Entry Name: | ADT1_HUMAN |