TBG1 Polyclonal Antibody, 100ul Cell Transfection Diseases associated with CEP68 include

Diseases associated with CEP68 include Retinitis Pigmentosa 28

the complex strongly stimulates DNA end joining

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The encoded protein acts as a dominant-negative regulator of transcription which is mediated by the retinoic acid receptor

This complex is composed partly of two structural maintenance of chromosomes (SMC) proteins

TBG1 Polyclonal Antibody, 100ul Cell Transfection Diseases associated with CEP68 includeThis gene encodes a member of the tubulin superfamily. The encoded protein localizes to the centrosome where it binds to microtubules as part of a complex referred to as the gamma tubulin ring complex. The protein mediates microtubule nucleation and is required for microtubule formation and progression of the cell cycle. A pseudogene of this gene is found on chromosome 7.