SLC25A4 Antibody - N-terminal region
Cat# ARP43818_P050-25UL
Size : 25ul
Brand : Aviva Systems Biology
SLC25A4 Antibody - N-terminal region (ARP43818_P050)
| Datasheets/Manuals | Printable datasheet for anti-SLC25A4 (ARP43818_P050) antibody |
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| Tested Species Reactivity | Human, Rat |
|---|---|
| Predicted Species Reactivity | Human, Mouse, Rat, Cow, Dog, Goat, Guinea Pig, Horse, Rabbit, Sheep, Zebrafish |
| Product Format | Liquid. Purified antibody supplied in 1x PBS buffer with 0.09% (w/v) sodium azide and 2% sucrose. |
| Clonality | Polyclonal |
| Host | Rabbit |
| Application | IHC, WB |
| Reconstitution and Storage | For short term use, store at 2-8C up to 1 week. For long term storage, store at -20C in small aliquots to prevent freeze-thaw cycles. |
| Immunogen | The immunogen is a synthetic peptide directed towards the N terminal region of human SLC25A4 |
| Purification | Affinity Purified |
| Predicted Homology Based on Immunogen Sequence | Cow: 100%; Dog: 100%; Goat: 100%; Guinea Pig: 100%; Horse: 93%; Human: 100%; Mouse: 100%; Rabbit: 100%; Rat: 100%; Sheep: 100%; Zebrafish: 86% |
| Peptide Sequence | Synthetic peptide located within the following region: LLQVQHASKQISAEKQYKGIIDCVVRIPKEQGFLSFWRGNLANVIRYFPT |
| Concentration | 0.5 mg/ml |
| Blocking Peptide | For anti-SLC25A4 (ARP43818_P050) antibody is Catalog # AAP43818 (Previous Catalog # AAPS14103) |
| Sample Type Confirmation | SLC25A4 is supported by BioGPS gene expression data to be expressed in RPMI 8226 |
| Enhanced Validation | Relative Expression (Western Blot)  |
| Gene Symbol | SLC25A4 |
|---|---|
| Gene Full Name | Solute carrier family 25 (mitochondrial carrier; adenine nucleotide translocator), member 4 |
| Alias Symbols | T1, ANT, AAC1, ANT1, PEO2, PEO3, ANT 1, PEOA2, MTDPS12, MTDPS12A |
| NCBI Gene Id | 291 |
| Protein Name | ADP/ATP translocase 1 |
| Description of Target | 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 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. |
| Uniprot ID | Q05962 |
| Protein Accession # | NP_001142 |
| Nucleotide Accession # | NM_001151 |
| Protein Size (# AA) | 298 |
| Molecular Weight | 33 kDa |
| Protein Interactions | UBC; MDM2; PARK2; CLN5; CLN3; UBL4A; RPLP0P6; RPL10L; UQCRFS1P1; UQCRC1; RPS3A; RPS2; RPSA; GALNT2; UBD; COPS5; CDK2; TCF3; SUMO4; ICT1; NFKBIA; MGMT; PPID; PPIF; BAX; AR; PRKCE; NR3C1; |
