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Huntingtin 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.

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Price From: €165.00
Available
Ref : 00012849

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Product Code pab0869-P
Immunogen synthetic peptide derived from N terminal part of human Huntingtin
Target Specificity Reacts with the human Huntingtin protein. Cross react with mouse and rat protein due to sequence homology.
Name Huntingtin
Uniprot ID P42858
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Product type Primary antibodies
Clonality Polyclonal antibody
Produced in Rabbit
Species Human, Mouse, Rat
Labelling None
Appearance Lyophilized powder
Conc. / Activity 1 mg/ml
Form Purified (protein A)
Constituents Tris 0,1M, glycine 0,1M, sucrose 2%
Preservatives None
Recommendations Must be reconstituted in distilled water.
Storage Lyophilized powder stable for a minimum of 2 years at -20°C.
Store reconstituted antibodies at +4°C.
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
Print datasheet

Huntingtin antibody

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