KRCC1 Polyclonal Antibody (E-AB-53125)
For research use only.
| Verified Samples |
Verified Samples in IHC: Human colorectal cancer, Human liver cancer |
| Dilution | IHC 1:50-1:200 |
| Isotype | IgG |
| Host | Rabbit |
| Reactivity | Human |
| Applications | IHC |
| Clonality | Polyclonal |
| Immunogen | Fusion protein of human KRCC1 |
| Abbre | KRCC1 |
| Synonyms | CHBP2, Cryptogenic hepatitis-binding protein 2, KRCC1, Lysine-rich coiled-coil protein 1, cryptogenic hepatitis binding protein, lysine rich coiled coil 1 |
| Swissprot | |
| Concentration | 1.08 mg/mL |
| Buffer | Phosphate buffered solution, pH 7.4, containing 0.05% stabilizer and 50% glycerol. |
| Purification Method | Antigen 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 | KRCC1 (lysine-rich coiled-coil 1), also known as CHBP2 (cryptogenic hepatitis-binding protein 2), is a 259 amino acid protein that is encoded by a gene located on human chromosome 2p11.2.Consisting of 237 million bases, chromosome 2 is the second largest human chromosome and encodes over 1,400 genes.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. |
Other Clones
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Other Formats
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Unconjugated
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