ERCC8 Rabbit anti-Human, Mouse, Polyclonal, Invitrogen
Rabbit Polyclonal Antibody
Manufacturer: Invitrogen PA524436
DescriptionThis gene encodes a WD repeat protein, which interacts with Cockayne syndrome type B (CSB) protein and with p44 protein, a subunit of the RNA polymerase II transcription factor IIH. Mutations in this gene have been identified in patients with hereditary disease Cockayne syndrome (CS). CS cells are abnormally sensitive to ultraviolet radiation and are defective in the repair of transcriptionally active genes.
|PBS with 0.09% sodium azide|
|CKN1, CSA, Cockayne syndrome WD-repeat protein CSA, DNA excision repair protein ERCC-8, cockayne syndrome WD repeat protein CSA|
|-20° C, Avoid Freeze/Thaw Cycles|
|Immunohistochemistry, Western Blot|
|KLH conjugated synthetic peptide between 210-238 amino acids from the central region of human ERCC8|
|Antigen affinity chromatography|
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