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Invitrogen™ FAM111B Polyclonal Antibody
Rabbit Polyclonal Antibody
Supplier: Invitrogen™ PA5103333
Description
Antibody detects endogenous levels of total F111B.
FAM111B is a 734 amino acid protein that is encoded by a gene that maps to human chromosome 11, which makes up around 4% of human genomic DNA and isconsidered a gene and disease association dense chromosome.The chromosome 11 encoded Atmgene isimportant for regulation ofcellcycle arrest and apoptosisfollowing double strand DNA breaks. Atmmutation leads to the disorderknown as ataxia-telangiectasia. The blood disorders Sickle cell anemia and beta thalassemia are caused by HBB genemutations. Wilms' tumors, WAGR syndrome and Denys-Drash syndrome are associatedwithmutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associatedwith defectsin chromosome 11.
Specifications
FAM111B | |
Polyclonal | |
Unconjugated | |
FAM111B | |
Cancer-associated nucleoprotein; CANP; FAM111B; family with sequence similarity 111 member B; family with sequence similarity 111, member B; POIKTMP; Protein FAM111B | |
Rabbit | |
Affinity chromatography | |
RUO | |
374393 | |
-20°C | |
Liquid |
Immunohistochemistry (Paraffin), Western Blot, Immunocytochemistry | |
1 mg/mL | |
PBS with 50% glycerol and 0.02% sodium azide; pH 7.4 | |
Q6SJ93 | |
FAM111B | |
A synthesized peptide derived from human FAM111B(Accession Q6SJ93), corresponding to amino acid residues L44-R94. | |
100 μL | |
Primary | |
Human, Mouse | |
Antibody | |
IgG |
Safety and Handling
WARNING: Cancer - www.P65Warnings.ca.gov
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