FUNDC2 Polyclonal Antibody (E-AB-18928)
For research use only.
| Verified Samples |
Verified Samples in IHC: Human tonsil, Human thyroid cancer |
| Dilution | IHC 1:50-1:300 |
| Isotype | IgG |
| Host | Rabbit |
| Reactivity | Human |
| Applications | IHC |
| Clonality | Polyclonal |
| Immunogen | Fusion protein of human FUNDC2 |
| Abbre | FUNDC2 |
| Synonyms | Cervical cancer oncogene 3, Cervical cancer proto oncogene 3 protein, DC44, FLJ33773, FUN14 domain containing 2, FUN14 domain containing protein 2, FUNDC 2, HCBP 6, HCBP6, HCC 3, HCC3, Hepatitis C virus core binding protein 6, MGC131676, MGC2495, OTT, OTTHUMP00000015441 |
| Swissprot | |
| Cellular Localization | Mitochondrial |
| Concentration | 0.72 mg/mL |
| Buffer | Phosphate buffered solution, pH 7.4, containing 0.05% stabilizer and 50% glycerol. |
| Purification Method | Antigen affinity purification |
| Research Areas | Epigenetics and Nuclear Signaling, Metabolism, Microbiology, Signal transduction |
| 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 | FUNDC2 (FUN14 domain-containing protein 2), also known as HCC-3 (cervical cancer proto-oncogene 3 protein), HCBP6 (hepatitis C virus core-binding protein 6) or DC44, is a 189 amino acid protein belonging to the FUN14 family. The gene encoding FUNDC2 maps to human chromosome Xq28. The X and Y chromosomes are the human sex chromosomes. Chromosome X consists of about 153 million base pairs and nearly 1,000 genes. The combination of an X and Y chromosome lead to normal male development while two copies of X lead to normal female development. More than one copy of the X chromosome with a Y chromosome causes Klinefelter's syndrome. A single copy of X alone leads to Turner's syndrome. More than 2 copies of the X chromosome, in the absence of a Y chromosome, is known as Triple X syndrome. Color blindness, hemophilia, and Duchenne muscular dystrophy are well known X chromosome-linked conditions which affect males more frequently as males carry a single X chromosome. |
Other Clones
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Other Formats
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Unconjugated
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