Huntingtin pS17 antibody

Huntington disease protein (HD protein)
Gene name : HTT, HD, IT15
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00012854
Defects in HTT are the cause of Huntington disease (HD). HD is an autosomal dominant neurodegenerative disorder characterized by involuntary movements (chorea), general motor impairment, psychiatric disorders and dementia.
More Information
ID Covalab pab0871-IP
Product type Primary antibodies
Clonality Polyclonal antibody
Raised in Rabbit
Immunogen synthetic peptide derived from N terminal part of human Huntingtin containing a phospho serine at position 17
Activity cross reaction Reacts with the human Huntingtin phosphoserine 17. Cross react with mouse and rat protein due to sequence homology.
Species Hu, Ms, Rat
Labelling None
Form Antigen affinity purified
Preservative 0.02% NaN3
Storage instructions For extended periods store in aliquots at -20°C.
Antibodies are guaranteed for 6 month from date of receipt.
Target Huntingtin pS17
Uniprot ID P42858
Applications ELISA, ICC, WB
Working dilutions Optimal dilutions should be determined by the end user.
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