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FANCA Polyclonal Antibody

Polyclonal antibody

Specification

BYab-03868

  • 50UL $180 100UL $255
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Host
Reactiveness
Use
Molecular weight (DA)
Immunogen
The antiserum was produced against synthesized peptide derived from human FANCA. AA range:1121-1170
Specificity
FANCA Polyclonal Antibody detects endogenous levels of FANCA protein.
Source
Formulation
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
Dilution rate
IHC: 1/100 - 1/300. ELISA: 1/5000.. IF 1:50-200
Purification process (Immunogen)
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration
1 mg/ml
Background
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, Jul
Function
disease:Defects in FANCA are a cause of Fanconi anemia (FA) [MIM:227650]. FA is a genetically heterogeneous, autosomal recessive disorder characterized by progressive pancytopenia, a diverse assortment of congenital malformations, and a predisposition to the development of malignancies. At the cellular level it is associated with hypersensitivity to DNA-damaging agents, chromosomal instability (increased chromosome breakage), and defective DNA repair.,function:DNA repair protein that may operate in a postreplication repair or a cell cycle checkpoint function. May be involved in interstrand DNA cross-link repair and in the maintenance of normal chromosome stability.,PTM:Phosphorylated upon DNA damage, probably by ATM or ATR. Phosphorylation is required for the formation of the nuclear complex. Not phosphorylated in cells derived from groups A, B, C, E, F, G, and H.,subcellular location:Th
Gene Name
FANCA
Protein name
Fanconi anemia group A protein
Abbreviation
FANCA
Other name
FANCA; FAA; FACA; FANCH; Fanconi anemia group A protein; Protein FACA
Fields
>>Fanconi anemia pathway
Human gene ID
2175
Human protein sequence Database
O15360
Mouse gene ID
Mouse protein sequence database
Q9JL70
Rat gene ID
Rat protein sequence database
Cellular localization
Nucleus. Cytoplasm. The major form is nuclear. The minor form is cytoplasmic.
Tissue expression
Cervix,Epithelium,Lymphoblast,Ovary,PCR rescued clones,
Storage
-20°C/1 year

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FANCA Polyclonal Antibody

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