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Dymeclin Proteins

(Dymeclin (DYM))

This gene encodes a protein which is necessary for normal skeletal development and brain function. Mutations in this gene are associated with two types of recessive osteochondrodysplasia, Dyggve-Melchior-Clausen (DMC) dysplasia and Smith-McCort (SMC) dysplasia, which involve both skeletal defects and mental retardation. [provided by RefSeq, Jul 2008].

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5 results

Dymeclin Protein (DYM) (His tag)

DYM Origin: Human Host: Escherichia coli (E. coli) Recombinant SDS, WB, ELISA

Catalog No. ABIN7576695

Dymeclin Protein (DYM) (AA 546-669) (His tag)

DYM Origin: Human Host: Escherichia coli (E. coli) Recombinant > 95 % SDS, WB, Imm, PC

Catalog No. ABIN7396361

Dymeclin Protein (DYM) (Myc-DYKDDDDK Tag)

DYM Origin: Human Host: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD

Validation with Western Blot

1 image

Catalog No. ABIN2719847

Dymeclin Protein (DYM) (AA 2-674) (His tag)

DYM Origin: Rat Host: Yeast Recombinant > 90 % ELISA

Catalog No. ABIN7584172

Dymeclin Protein (DYM)

DYM Origin: Human Host: Escherichia coli (E. coli) Recombinant > 95 % SDS, WB, ELISA, IP

Catalog No. ABIN6303931

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