ARG54749

anti-KMT3A / SETD2 antibody

anti-KMT3A / SETD2 antibody for IHC-Formalin-fixed paraffin-embedded sections and Human

Gene Regulation antibody

Overview

Product Description Rabbit Polyclonal antibody recognizes KMT3A / SETD2
Tested Reactivity Hu
Predict Reactivity Ms
Tested Application IHC-P
Host Rabbit
Clonality Polyclonal
Target Name KMT3A / SETD2
Antigen Species Human
Immunogen KLH-conjugated synthetic peptide corresponding to aa. 21-50 (N-terminus) of Human KMT3A / SETD2 (NP_054878.5).
Conjugation Un-conjugated
Alternate Names HIF-1; SET domain-containing protein 2; SET2; Huntingtin-interacting protein B; Huntingtin yeast partner B; KMT3A; Huntingtin-interacting protein 1; hSET2; EC 2.1.1.43; HBP231; Lysine N-methyltransferase 3A; HIP-1; p231HBP; HSPC069; Histone-lysine N-methyltransferase SETD2; HYPB

Application Instructions

Application Suggestion
Tested Application Dilution
IHC-PAssay-dependent
Application Note * The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist.

Properties

Form Liquid
Purification Purification with Protein G.
Buffer PBS and 0.09% (W/V) Sodium azide
Preservative 0.09% (W/V) Sodium azide
Storage Instruction For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C or below. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use.
Note For laboratory research only, not for drug, diagnostic or other use.

Bioinformation

Database Links

GeneID: 29072 Human SETD2

Swiss-port # Q9BYW2 Human Histone-lysine N-methyltransferase SETD2

Gene Symbol SETD2
Gene Full Name SET domain containing 2
Background 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, Aug 2008]
Function Histone methyltransferase that specifically trimethylates 'Lys-36' of histone H3 (H3K36me3) using dimethylated 'Lys-36' (H3K36me2) as substrate. Represents the main enzyme generating H3K36me3, a specific tag for epigenetic transcriptional activation. Plays a role in chromatin structure modulation during elongation by coordinating recruitment of the FACT complex and by interacting with hyperphosphorylated POLR2A. Acts as a key regulator of DNA mismatch repair in G1 and early S phase by generating H3K36me3, a mark required to recruit MSH6 subunit of the MutS alpha complex: early recruitment of the MutS alpha complex to chromatin to be replicated allows a quick identification of mismatch DNA to initiate the mismatch repair reaction. H3K36me3 also plays an essential role in the maintenance of a heterochromatic state, by recruiting DNA methyltransferase DNMT3A. H3K36me3 is also enhanced in intron-containing genes, suggesting that SETD2 recruitment is enhanced by splicing and that splicing is coupled to recruitment of elongating RNA polymerase. Required during angiogenesis. Recruited to the promoters of adenovirus 12 E1A gene in case of infection, possibly leading to regulate its expression. [UniProt]
Cellular Localization Nucleus. Chromosome
Research Area Gene Regulation antibody
Calculated MW 288 kDa
PTM May be automethylated.