|Application ||IHC-P, E|
|Calculated MW||19738 Da|
|Dilution||ELISA, IHC-P (7.5 µg/ml)|
|Other Names||CETN2, Caltractin isoform 1, Centrin-2, CALT, Caltractin, isoform 1, Centrin, EF-hand protein, 2, CEN2, Centrin 2|
|Target/Specificity||Human CETN2 / Centrin 2|
|Reconstitution & Storage||Caprylic acid and ammonium sulfate precipitation|
|Precautions||Anti-CETN2 / Centrin 2 Antibody (aa1-172) is for research use only and not for use in diagnostic or therapeutic procedures.|
|Function||Plays a fundamental role in microtubule organizing center structure and function. Required for centriole duplication and correct spindle formation. Has a role in regulating cytokinesis and genome stability via cooperation with CALM1 and CCP110. The XPC complex is proposed to represent the first factor bound at the sites of DNA damage and together with other core recognition factors, XPA, RPA and the TFIIH complex, is part of the pre-incision (or initial recognition) complex. The XPC complex recognizes a wide spectrum of damaged DNA characterized by distortions of the DNA helix such as single-stranded loops, mismatched bubbles or single-stranded overhangs. The orientation of XPC complex binding appears to be crucial for inducing a productive NER. XPC complex is proposed to recognize and to interact with unpaired bases on the undamaged DNA strand which is followed by recruitment of the TFIIH complex and subsequent scanning for lesions in the opposite strand in a 5'-to-3' direction by the NER machinery. Cyclobutane pyrimidine dimers (CPDs) which are formed upon UV-induced DNA damage esacpe detection by the XPC complex due to a low degree of structural perurbation. Instead they are detected by the UV-DDB complex which in turn recruits and cooperates with the XPC complex in the respective DNA repair.|
|Cellular Location||Cytoplasm, cytoskeleton, microtubule organizing center, centrosome, centriole. Nucleus Note=Centrosome of S-phase, interphase and mitotic cells|
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