FANCG (phospho Ser383) rabbit pAb
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 G. [provided by RefSeq, Jul 2008],
Product Specifications
Background
Product Name Alternative
FANCG; XRCC9; Fanconi anemia group G protein; Protein FACG; DNA repair protein XRCC9
UniProt
O15287
Swiss Prot
O15287
Reactivity
Human; Rat; Mouse
Immunogen
Synthesized phospho-peptide around the phosphorylation site of human FANCG (phospho Ser383)
Target
FANCG
Clonality
Polyclonal
Source
Rabbit
Applications
WB; ELISA
Concentration
1 mg/ml
Dilution
Western Blot: 1/500 - 1/2000. ELISA: 1/40000. Not yet tested in other applications.
Buffer
-20°C/1 year
Molecular Weight
69kD
Storage Conditions
-20°C/1 year
Observed Molecular Weight
69kD
Fragment
IgG
Subcellular Location
Nucleus . Cytoplasm . The major form is nuclear. The minor form is cytoplasmic.
Other Product Names
FANCG; XRCC9; Fanconi anemia group G protein; Protein FACG; DNA repair protein XRCC9
Gene ID (Human)
2189
Available Sizes
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