Amyotrophic lateral sclerosis with frontotemporal dementia, chromosome 9 open reading frame 72, C9orf72
Product description
ALSFTD (C9orf72) is considered to play a role in gender determination (1). Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG (2). Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster (3,4).1) Takada LT and Sha SJ. Neuropsychiatric features of C9orf72-associated behavioral variant frontotemporal dementia and frontotemporal dementia with motor neuron disease. Alzheimers Res. Ther. 2012; 4:38.
Immunogen
ALSFTD antibody was raised against a 19 amino acid peptide from near the carboxy terminus of human ALSFTD. The immunogen is located within amino acids 400 - 450 of ALSFTD.
Key Feature
Clonality
Polyclonal
Isotype
IgG
Host Species
Rabbit
Tested Applications
WB
ALSFTD antibody can be used for the detection of ALSFTD by Western blot at 1 - 2 μg/mL. Antibody can also be used for immunocytochemistry at 10 μg/ml.:
Western blot analysis of ALSFTD in HeLa cell lysate with ALSFTD antibody at 1 μg/ml.
Application
Immunocytochemistry of ALSFTD in A-20 cells with ALSFTD antibody at 10 μg/ml.
Positive Control
1) Cat. No. 1288 - A20 Cell Lysate
Application Notes
ALSFTD antibody can be used for the detection of ALSFTD by Western blot at 1 - 2 μg/mL. Antibody can also be used for immunocytochemistry at 10 μg/ml.:
Additional Information
Form
Liquid
Storage Instructions
ALSFTD antibody can be stored at 4˚C for three months and -20˚C, stable for up to one year.
Storage Buffer
ALSFTD Antibody is supplied in PBS containing 0.02% sodium azide.