FASTKD1 Polyclonal Antibody Store at -20°C
SKU: E-AB-11221-200
FASTKD1 Polyclonal Antibody Store at -20°C
| SKU # | E-AB-11221 |
| Reactivity | Human |
| Host | Rabbit |
| Applications | IHC |
Product Details
| Isotype | IgG |
| Host | Rabbit |
| Reactivity | Human |
| Applications | IHC |
| Clonality | Polyclonal |
| Immunogen | Recombinant protein of human FASTKD1 |
| Abbre | FASTKD1 |
| Synonyms | FAKD1, FAST kinase domain containing protein 1, FAST kinase domain-containing protein 1, FAST kinase domains 1, FASTKD1, FLJ21901, KIAA1800, OTTHUMP00000207008, OTTHUMP00000207010 |
| Swissprot | |
| Cellular Localization | Mitochondrion |
| Concentration | 0.5 mg/mL |
| Buffer | Phosphate buffered solution, pH 7.4, containing 0.05% stabilizer and 50% glycerol. |
| Purification Method | Affinity purification |
| Research Areas | Cell Biology |
| Conjugation | Unconjugated |
| Storage | Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles. |
| Shipping | The product is shipped with ice pack,upon receipt,store it immediately at the temperature recommended. |
Related Reagents
| Applications | Recommended Dilution |
| IHC | 1:100-1:300 |
Background
The second largest human chromosome, 2 consists of 237 million bases encoding over 1,400 genes and making up approximately 8% of the human genome.A number of genetic diseases are linked to genes on chromosome 2.Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene.The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8.An extremely rare recessive genetic disorder, Alstr m syndrome is due to mutations in the ALMS1 gene.Interestingly, chromosome 2 contains what appears to be a vestigial second centromere and vestigial telomeres which gives credence to the hypothesis that human chromosome 2 is the result of an ancient fusion of two ancestral chromosomes seen in modern form today in apes.