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Recombinant Human SMYD3/ZMYND1 Protein (GST Tag)– MSE Supplies LLC

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Recombinant Human SMYD3/ZMYND1 Protein (GST Tag)

SKU: PKSH031202-50

  • £54300
  • Save £6100



Recombinant Human SMYD3/ZMYND1 Protein (GST Tag)

 

SKU # PKSH031202
Expression Host Baculovirus-Insect Cells

 

 

Description

Synonyms KMT3E, ZMYND1, ZNFN3A1, bA74P14.1
Species Human
Expression Host Baculovirus-Insect Cells
Sequence Lys 35-Ser 369
Accession NP_073580.1
Calculated Molecular Weight 65.6 kDa
Observed Molecular Weight 58 kDa
Tag N-GST
Bio-activity Not validated for activity
  

 

Properties

Purity > 88 % as determined by reducing SDS-PAGE.
Endotoxin < 1.0 EU per μg of the protein as determined by the LAL method.
Storage Generally, lyophilized proteins are stable for up to 12 months when stored at -20 to -80℃. Reconstituted protein solution can be stored at 4-8℃ for 2-7 days. Aliquots of reconstituted samples are stable at < -20℃ for 3 months.
Shipping This product is provided as lyophilized powder which is shipped with ice packs.
Formulation Lyophilized from sterile 20mM Tris, 150mM NaCl, 0.5mM DTT, 0.5mM GSH, pH 8.0
Normally 5% - 8% trehalose, mannitol and 0.01% Tween 80 are added as protectants before lyophilization.
Please refer to the specific buffer information in the printed manual.
Reconstitution Please refer to the printed manual for detailed information.


Background

SET and MYND domain-containing protein 3, also known as Zinc finger MYND domain-containing protein 1, SMYD3, and ZMYND, is a member of the histone-lysine methyltransferase family. SMYD3 contains oneMYND-type zinc finger and oneSET domain. SMYD3 is a histone H3 lysine-4-specific methyltransferase. It is expressed in skeletal muscles and testis. It is overexpressed in a majority of colorectal carcinoma (CRC) and hepatocellular carcinoma (HCC). SMYD3 plays an important role in transcriptional regulation in human carcinogenesis. It activates the transcription of a set of downstream genes. Of these downstream genes, there are several oncogenes and genes associated with cell adhesion (including those of N-Myc, CrkL, Wnt10b, L-selectin, CD31 and galectin-4), which have been shown to have effects on cell viability, adhesion, migration and metastasis. Increased SMYD3 expression is essential for the proliferation of breast cancer cells. SMYD3 may be a promising new target of therapeutic intervention for the treatment of cancers or other pathological processes associated with cell adhesion and migration.