Recombinant Human DYM Protein, His-tagged

• Cat.No.: DYM-679H
• Product Overview: Recombinant Human DYM(Ser546~Asp669) fused with His tag at N-terminal was expressed in E. coli.

Specification

• Description: This gene encodes a protein which regulates Golgi-associated secretory pathways that are essential to endochondral bone formation during early development. This gene is also believed to play a role in early brain development. This gene is widely expressed in embryos and is particularly abundant in chodrocytes and brain tissues. It encodes a peripheral membrane protein which shuttles between the cytosol and Golgi complex. Mutations in this gene are associated with two types of recessive osteochondrodysplasia: Dyggve-Melchior-Clausen (DMC) dysplasia and Smith-McCort (SMC) dysplasia.
• Source: E. coli
• Species: Human
• Tag: His
• Form: PBS, pH7.4, containing 0.01% SKL, 1mM DTT, 5% Trehalose and Proclin300.
• Molecular Mass: 16.2kDa
• Protein length: Ser546~Asp669
• Endotoxin: <1.0EU per 1ug (determined by the LAL method)
• Purity: > 95%
• Applications: Positive Control; Immunogen; SDS-PAGE; WB.
  If bio-activity of the protein is needed, please check active protein
• Stability: The thermal stability is described by the loss rate. The loss rate was determined by accelerated thermal degradation test, that is, incubate the protein at 37 centigrade for 48h, and no obvious degradation and precipitation were observed. The loss rate is less than 5% within the expiration date under appropriate storage condition.
• Storage: Avoid repeated freeze/thaw cycles. Store at 2-8 centigrade for one month. Aliquot and store at -80 centigrade for 12 months.
• Reconstitution: Reconstitute in PBS or others

Gene Information

• Gene Name: DYM dymeclin [ Homo sapiens ]
• Official Symbol: DYM
• Synonyms: DYM; dymeclin; DMC; FLJ20071; SMC; dyggve-Melchior-Clausen syndrome protein; FLJ90130
• Gene ID: 54808
• mRNA Refseq: NM_017653
• Protein Refseq: NP_060123
• MIM: 607461
• UniProt ID: Q7RTS9