Fanconi Anemia (FA)
Fanconi anemia (FA) is an autosomal recessive genetic disorder resulting in symptoms that include chromosomal breakage, bone marrow failure, hypersensitivity to DNA cross-linking agents (such as mitomycin C), and a predisposition to cancer (1). In response to DNA damage, the FA nuclear complex (FANCA, FANCB, FANCC, FANCE, FANCF, FANCG, FANCM) induces mono-ubiquitination of FANCD2 and FANCI (2). Monoubiquitination of FANCD2 induces localization of FANCD2 to sites of DNA damage, where it interacts with BRCA1. FANCJ/BRIP1, FANCD1/BRCA2, and FANCN/PALB2 are also recruited to sites of DNA damage (3).

Fanconi Anemia Pathway (4)
| Catalog# | Product Name | Reactivity | Application |
|---|---|---|---|
| AMRe84275 | FANCA Rabbit Monoclonal | Human | WB,IP |
| AMRe01974 | FANCB Rabbit Monoclonal Antibody | Human,Mouse | WB |
| AMRe10826 | FANCD2 (16Q3) Rabbit Monoclonal Antibody | Human,Mouse,Rat | WB,IHC-P,ICC/IF,FC,IP,IF-P |
| AMM86025 | BRCA2 Mouse Monoclonal Antibody | Human | WB |
| AMM82390 | BRIP1 Mouse Monoclonal Antibody | Human | IHC,FC,ELISA |
| APS0635 | HRP-conjugated Polyclonal Goat Anti-Rabbit IgG(H+L) Secondary Antibody | Rabbit | ELISA, WB, Dot blot |
| AMre80004 | GAPDH (12R9) Rabbit Monoclonal Antibody | Human,Mouse,Rat,Rabbit,Dog,Monkey | WB,ELISA |
Related Products
- Alter BP. Fanconi's anemia and malignancies. Am J Hematol. 1996 Oct;53(2):99-110.[PMID: 8892734].
- Fei P, Yin J, Wang W. New advances in the DNA damage response network of Fanconi anemia and BRCA proteins. FAAP95 replaces BRCA2 as the true FANCB protein. Cell Cycle. 2005 Jan;4(1):80-6.[PMID: 15611632].
- Garcia-Higuera I, Taniguchi T, Ganesan S, Meyn MS, Timmers C, Hejna J, Grompe M, D'Andrea AD. Interaction of the Fanconi anemia proteins and BRCA1 in a common pathway. Mol Cell. 2001 Feb;7(2):249-62.[PMID: 11239454].
- Moreno OM, Paredes AC, Suarez-Obando F, Rojas A. An update on Fanconi anemia: Clinical, cytogenetic and molecular approaches (Review). Biomed Rep. 2021 Sep;15(3):74.[PMID: 34405046].
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