Tag/Conjugate
Unconjugated
Antigen Description
The protein encoded by this gene is a potential transmembrane protein that is phosphorylated upon DNA damage. Defects in this gene are a cause of spastic paraplegia type 11 (SPG11). Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2009]
Synonyms
SPG11; spastic paraplegia 11 (autosomal recessive); KIAA1840; spatacsin; spastic paraplegia 11 protein; colorectal carcinoma-associated protein
Citations
Have you cited CDBP6176 in a publication?
Let us know and earn a reward for your research.
| Product Name |
Cat. No. |
Applications |
Host Species |
Datasheet |
Price |
Add to Basket |
| Product Name |
Cat. No. |
Applications |
Host Species |
Datasheet |
Price |
Add to Basket |
Murmu, RP; Martin, E; et al. Cellular distribution and subcellular localization of spatacsin and spastizin, two proteins involved in hereditary spastic paraplegia. MOLECULAR AND CELLULAR NEUROSCIENCE 47:191-202(2011).
Kuru, S; Yoshida, M; et al. Immunohistochemical localization of spatacsin in alpha-synucleinopathies. NEUROPATHOLOGY 34:135-139(2014).