FASTKD1 Polyclonal Antibody
| 规格： | / 20μL / 60μL / 120μL / 200μL |
| 价格： | / ￥420 / ￥1010 / ￥1640 / ￥2365 |
货号：E-AB-11221
宿主: Rabbit
反应性: H
应用: IHC
Overview
| Synonyms | FAKD1,FAST kinase domain containing protein 1,FAST kinase domain-containing protein 1,FAST kinase domains 1,FASTKD1,FLJ21901,KIAA1800,OTTHUMP00000207008,OTTHUMP00000207010,FASTKD1抗体 |
| Swissprot | Q53R41 |
| Source | Rabbit |
| Reactivity | Human |
| Immunogen | Recombinant protein of human FASTKD1 |
| Application | IHC(Detection kit: E-IR-R213) |
| Recommended dilution | IHC,,1:100-1:300 |
| Concentration | 0.5 mg/mL |
| Clonality | Polyclonal |
Properties
| Cellular localization | Mitochondrion |
| Tissue specificity | Expression detected in spleen, thymus, testis, ovary, colon, heart, smooth muscle, kidney, brain, lung, liver and white adipose tissue with highest expression in heart. |
| Isotype | IgG |
| Purification | Affinity purification |
| Conjugation | Unconjugated |
| Storage instructions | Store at -20℃. Avoid freeze / thaw cycles. |
| Storage buffer | PBS with 0.05% sodium azide, 50% glycerol, PH7.3 |
| 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. |
