FANCL (Human) IP-WB Antibody Pair
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More Files
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Immunoprecipitation of FANCL transfected lysate using rabbit polyclonal anti-FANCL and Protein A Magnetic Bead (U0007), and immunoblotted with rabbit polyclonal anti-FANCL.
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Specification
Product Description
This IP-WB antibody pair set comes with one antibody for immunoprecipitation and another to detect the precipitated protein in western blot.
Reactivity
Human
Interspecies Antigen Sequence
Mouse (79); Rat (79)
Quality Control Testing
Immunoprecipitation-Western Blot (IP-WB)
Immunoprecipitation of FANCL transfected lysate using rabbit polyclonal anti-FANCL and Protein A Magnetic Bead (U0007), and immunoblotted with rabbit polyclonal anti-FANCL.
Supplied Product
Antibody pair set content:
1. Antibody pair for IP: rabbit polyclonal anti-FANCL (300 ul)
2. Antibody pair for WB: rabbit polyclonal anti-FANCL (50 ul)
Storage Instruction
Store reagents of the antibody pair set at -20°C or lower. Please aliquot to avoid repeated freeze thaw cycle. Reagents should be returned to -20°C storage immediately after use.
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Applications
Immunoprecipitation-Western Blot
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Gene Info — FANCL
Entrez GeneID
55120Gene Name
FANCL
Gene Alias
FAAP43, FLJ10335, PHF9, POG
Gene Description
Fanconi anemia, complementation group L
Omim ID
608111Gene Ontology
HyperlinkGene 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 L. Alternative splicing results in two transcript variants encoding different isoforms. [provided by RefSeq
Other Designations
PHD finger protein 9
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Interactome
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Pathway
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Disease
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