FASTKD1 Polyclonal Antibody (E-AB-15020)

For research use only.
Verified Samples |
Verified Samples in IHC: Human ovarian cancer |
Dilution | IHC 1:100-1:300 |
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 | 0.6 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. |
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, Alstrm 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. |
Other Clones
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Other Formats
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Unconjugated
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