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SETD2, Rabbit, Polyclonal Antibody, Abnova™
Rabbit polyclonal antibody raised against recombinant SETD2.
Supplier: Abnova Corporation PAB23943
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. [provided by RefSeq]
Sequence: NLGMTSPLPYDSLGYNAPHHPFAGYPPGYPMQAYVDPSNPNAGKVLLPTPSMDPVCSPAPYDHAQPLVGHSTEPLSAPPPVPVVPHVAAPVEVSSSQYVASpecifications
SETD2 | |
Polyclonal | |
Rabbit polyclonal antibody raised against recombinant SETD2. | |
In PBS, pH 7.5 (40% glycerol, 0.02% sodium azide) | |
FLJ16420/FLJ22472/FLJ23184/FLJ45883/FLJ46217/HIF-1/HSPC069/HYPB/KIAA1732/KMT3A/SET2/p231HBP | |
Rabbit | |
Antigen affinity purification | |
RUO | |
29072 | |
Store at 4°C. For long term storage store at -20°C. Aliquot to avoid repeated freezing and thawing. |
|
IgG |
Immunohistochemistry (PFA fixed) | |
Unconjugated | |
Immunohistochemistry (1:1000-1:2500) The optimal working dilution should be determined by the end user. | |
SETD2 | |
SETD2 | |
Recombinant protein corresponding to amino acids of human SETD2. | |
100 μL | |
Primary | |
Human | |
Liquid |
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For Research Use Only