Cell Signaling Technology

Product Pathways - Protein Stability

Rad23A (D7U7Z) Rabbit mAb #24555

HHR23A   RAD23A   Ubiquitin binding proteins  

No. Size Price
24555S 100 µl ( 10 western blots ) ¥3,100.00 现货查询 购买询价
24555 carrier free & custom formulation / quantityemail request
Applications Dilution Species-Reactivity Sensitivity MW (kDa) Isotype
W 1:1000 Human,Mouse,Rat,Monkey, Endogenous 52 Rabbit IgG
IP 1:50

Species cross-reactivity is determined by western blot.

Applications Key: W=Western Blotting, IP=Immunoprecipitation,

Specificity / Sensitivity

Rad23A (D7U7Z) Rabbit mAb recognizes endogenous levels of total Rad23A protein. This antibody does not cross-react with Rad23B.

Source / Purification

Monoclonal antibody is produced by immunizing animals with a synthetic peptide corresponding to residues surrounding Gln214 of human Rad23A protein.

Western Blotting

Western Blotting

Western blot analysis of extracts from various cell lines using Rad23A (D7U7Z) Rabbit mAb.

Western Blotting

Western Blotting

Western blot analysis of extracts from 293T cells, mock transfected (-) or transfected with a construct expressing Myc/DDK-tagged full-length human Rad23A protein (hRad23A-Myc/DDK; +), using Rad23A (D7U7Z) Rabbit mAb.



Immunoprecipitation of Rad23A from 293T cell extracts. Lane 1 is 10% input, lane 2 is Rabbit (DA1E) mAb IgG XP® Isotype Control #3900, and lane 3 is Rad23A (D7U7Z) Rabbit mAb. Western blot analysis was performed using Rad23A (D7U7Z) Rabbit mAb.


The yeast nucleotide excision repair (NER) radiation sensitive protein 23 (rad23) and its human homologs Rad23A (hHR23A) and Rad23B (hHR23B) are critical components of the cellular machinery that recognize DNA lesions and serve as receptors that target ubiquitinated substrates to the proteasome for degradation (1).

The UV excision repair protein Rad23A is a multi-domain scaffold protein that plays an important role in ubiquitin-dependent proteasomal degradation. Rad23A protein contains an amino-terminal ubiquitin-like (UBL) domain and two ubiquitin binding domains, UBA1 and UBA2, that flank an XPC binding domain (2). Rad23A is thought to form a closed conformation that is dictated by an intramolecular interaction between the UBL and UBA domains. Binding of the Rad23A UBL domain to the S5a/PSMD4 subunit of the proteasome lid disrupts the intramolecular UBL-UBA association within Rad23A and promotes its association with the proteasome (3). Research studies show that Rad23A can be recruited to the proteasome through an interaction between its UBL domain and the S2/PSMD2 proteasome subunit (4). The UBA domains of Rad23A bind mono- and polyubiquitin and are thought to shuttle proteins modified with Lys48-linked polyubiquitin chains to the proteasome for degradation (1,5-7). In addition to its role as an ubiquitin-binding protein, Rad23A also participates in nucleotide excision repair (NER) by binding and stabilizing the NER DNA binding protein XPC (2,8).

  1. Verma, R. et al. (2004) Cell 118, 99-110.
  2. Masutani, C. et al. (1994) EMBO J 13, 1831-43.
  3. Walters, K.J. et al. (2003) Proc Natl Acad Sci U S A 100, 12694-9.
  4. Elsasser, S. et al. (2002) Nat Cell Biol 4, 725-30.
  5. Raasi, S. et al. (2005) Nat Struct Mol Biol 12, 708-14.
  6. Nathan, J.A. et al. (2013) EMBO J 32, 552-65.
  7. Elsasser, S. et al. (2004) J Biol Chem 279, 26817-22.
  8. Ng, J.M. et al. (2003) Genes Dev 17, 1630-45.

Application References

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