For research use only.
| Verified Samples |
Verified Samples in IHC: Human tonsil, Human esophagus cancer |
| Dilution | IHC 1:40-1:200 |
| Clonality | Polyclonal |
| Immunogen | Fusion protein of human SCCPDH |
| Abbre | SCCPDH |
| Synonyms | CGI 49, CGI49, FLJ43187, Probable saccharopine dehydrogenase, SCCPDH, SCPDH, Saccharopine dehydrogenase |
| Swissprot | |
| Cellular Localization | Extracellular region or secreted, extracellular region, Mitochondrion, Nucleus, Other locations: lipid droplet, membrane, midbody, platelet alpha granule lumen. |
| Concentration | 0.84 mg/mL |
| Buffer | PBS with 0.05% NaN3 and 40% Glycerol,pH7.4 |
| Purification Method | Antigen affinity purification |
| Research Areas | Metabolism, 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 | SCCPDH (Probable saccharopine dehydrogenase) is a 429 amino acid protein that belongs to the saccharopine dehydrogenase family. The SCCPDH gene is conserved in chimpanzee, dog, cow, mouse, rat, chicken, fruit fly, mosquito and C.elegans, and maps to human chromosome 1q44. Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma. |
Other Clones
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Other Formats
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Unconjugated
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