Product description

Huntington's disease (HD), a neurodegenerative disorder characterized by loss of striatal neurons, is caused by an expansion of a polyglutamine tract in the HD protein huntingtin. This gene encodes a protein belonging to a class of huntingtin interacting proteins characterized by WW motifs. This protein is a histone methyltransferase that is specific for lysine-36 of histone H3, and methylation of this residue is associated with active chromatin. This protein also contains a novel transcriptional activation domain and has been found associated with hyperphosphorylated RNA polymerase II.

Specifications
Applications
WB, IF
Host
Rabbit
Clonality
Polyclonal
Isotype
IgG
Supplier
Epigentek
Shipping & storage
Shipping condition
Blue Ice
Storage temperature
-20°C

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SETD2 Polyclonal Antibody

A-3720-100

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SETD2 Polyclonal Antibody

A-3720-100

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