Cell Signaling Technology

Product Pathways - DNA Damage

FANCA (D1L2Z) Rabbit mAb #14657

No. Size Price
14657S 100 µl ( 10 western blots ) ¥3,250.00 现货查询 购买询价
14657 carrier free & custom formulation / quantityemail request
Applications Dilution Species-Reactivity Sensitivity MW (kDa) Isotype
W 1:1000 Human, Endogenous 160 Rabbit IgG
IP 1:100

Species cross-reactivity is determined by western blot.

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

Specificity / Sensitivity

FANCA (D1L2Z) Rabbit mAb recognizes endogenous levels of total FANCA protein.

Source / Purification

Monoclonal antibody is produced by immunizing animals with a synthetic peptide corresponding to residues surrounding Ala514 of human FANCA protein.



Immunoprecipitation of FANCA from 293T cell extracts using Rabbit (DA1E) mAb IgG XP® Isotype Control #3900 (lane 2) or FANCA (D1L2Z) Rabbit mAb (lane 3). Lane 1 is 10% input. Western blot was performed using FANCA (D1L2Z) Rabbit mAb.

Western Blotting

Western Blotting

Western blot analysis of extracts from various cell lines using FANCA (D1L2Z) Rabbit mAb (upper) and α-Actinin (D6F6) XP® Rabbit mAb #6487 (lower). As expected, GM06914 cells are negative for FANCA.


Fanconi anemia (FA) is an autosomal recessive genetic disorder that results in chromosomal breakage, bone marrow failure, hypersensitivity to DNA cross-linking agents (such as mitomycin C), and a predisposition to cancer (1). The ubiquitously expressed FA complementation group A protein (FANCA, FAA) is a component of the FA nuclear complex that also contains FANCB, FANCC, FANCE, FANCF, FANCG, FANCL, and FANCM. In response to DNA damage, the FA nuclear complex induces mono-ubiquitination of FANCD2 and FANCI (2). FANCJ/BRIP1, FANCD1/BRCA2 and FANCN/PALB2 are then recruited to sites of DNA damage along with other DNA repair proteins. FA signaling is important in maintenance of chromosome stability and control of mitosis (3).

DNA-damage-dependent localization and stability of FANCA protein regulates FA complex function and localization. Interaction between FANCA protein and the Hsp90 chaperone protein regulates FANCA protein stability and turnover, and may play a role in controlling the FA DNA damage pathway (4). Mutations in the corresponding FANCA gene are responsible for the majority of cases of Fanconi anemia (5).

  1. Alter, B.P. (1996) Am J Hematol 53, 99-110.
  2. Fei, P. et al. (2005) Cell Cycle 4, 80-6.
  3. Nalepa, G. and Clapp, D.W. (2014) F1000Prime Rep 6, 23.
  4. Oda, T. et al. (2007) Blood 109, 5016-26.
  5. Yuan, F. et al. (2010) Front Biosci (Landmark Ed) 15, 1131-49.

Application References

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