Products

Western Blot (Cell lysate)

Western blot using FANCA polyclonal antibody (Cat # PAB10045) shows detection of a band at ~133 KDa (arrowhead) corres-ponding to FANCA in HeLa whole cell lysates.
The identity of the lower molecular weight bands is unknown, but may represent breakdown products.
Approximately 35 ug of lysate was separated by 4-20% Tris Glycine SDS-PAGE.
After blocking, the membrane was probed for 2 h at room temperature with the primary antibody diluted to 1:1,500.
The membrane was washed and reacted with a 1:10,000 dilution of IRDye™800 conjugated Gt-a-Rabbit IgG [H&L] for 45 min at room temperature (800 nm channel, green).
Molecular weight estimation was made by comparison to prestained MW markers indicated at left (700 nm channel, red).
IRDye™800 fluorescence images were captured using the Odyssey® Infrared Imaging System developed by LI-COR.
IRDye is a trademark of LI-COR, Inc.

Western Blot (Transfected lysate)

Western blot using FANCA polyclonal antibody (Cat # PAB10045) shows detection of FANCA only in FANCA transfected GM6914 cell lysates.
No staining is seen in lysates prepared from FANCA (-/-) cells in the absence of FANCA transfection.
Modified from Smogorzewska et al (2007) Cell 129, 289-301.

Enzyme-linked Immunoabsorbent Assay

Entrez GeneID

2175

Protein Accession#

NP_000126;O15360

Gene Name

FANCA

Gene Alias

FA, FA-H, FA1, FAA, FACA, FAH, FANCH, MGC75158

Gene Description

Fanconi anemia, complementation group A

Omim ID

227650 607139

Gene Ontology

Hyperlink

Gene Summary

The Fanconi anemia complementation group (FANC) currently includes FANCA, FANCB, FANCC, FANCD1 (also called BRCA2), FANCD2, FANCE, FANCF, FANCG, FANCI, FANCJ (also called BRIP1), FANCL, FANCM and FANCN (also called PALB2). The previously defined group FANCH is the same as FANCA. Fanconi anemia is a genetically heterogeneous recessive disorder characterized by cytogenetic instability, hypersensitivity to DNA crosslinking agents, increased chromosomal breakage, and defective DNA repair. The members of the Fanconi anemia complementation group do not share sequence similarity; they are related by their assembly into a common nuclear protein complex. This gene encodes the protein for complementation group A. Alternative splicing results in multiple transcript variants encoding different isoforms. Mutations in this gene are the most common cause of Fanconi anemia. [provided by RefSeq

Other Designations

Fanconi anemia, complementation group H|Fanconi anemia, type 1