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Huntingtin pT3 antibody

Huntington disease protein (HD protein)
Gene name : HTT, HD, IT15
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.

If you want to order offline

orders@covalab.com - tel: +33 (0) 437 654 230 - fax: +33 (0) 437 289 416

€335.00
Available
Ref : 00012857

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Product Code pab0872-IP
Immunogen Synthetic peptide derived from N terminal part of human Huntingtin containing a phospho threonine at position 3
Target Specificity Reacts with the human Huntingtin phospho threonine 3. Cross react with mouse and rat protein due to sequence homology.
Name Huntingtin pT3
Uniprot ID P42858
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Product type Primary antibodies
Clonality Polyclonal antibody
Produced in Rabbit
Species Human, Mouse, Rat
Labelling None
Appearance Liquid
Form Antigen affinity purified
Preservatives None
Storage For extended periods store in aliquots at -20°C.
Antibodies are guaranteed for 6 month from date of receipt.
Applications Western Blot, Immunocytochemistry, ELISA
Working dilutions Optimal dilutions should be determined by the end user.
Research areas Apoptosis,Disease-related biomarkers,Neurology,Vesicle trafficking
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Huntingtin pT3 antibody

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