Dymeclin antibody

Principal name

Dymeclin antibody

Alternative names for Dymeclin antibody

DYM, Dyggve-Melchior-Clausen syndrome protein

SwissProt ID

B4F766 (Rat), Q5ZLW3 (Chick), Q6DCP6 (Xenla), Q7RTS9 (Human), Q8CHY3 (Mouse)

Gene ID

54808 (DYM)

Available reactivities

Hu (Human), Ms (Mouse), Rt (Rat)

Available hosts

Mouse, Rabbit

Available applications

Enzyme Immunoassay (E), Western blot / Immunoblot (WB), Paraffin Sections (P)

Background of Dymeclin antibody

Dyggve-Melchior-Clausen syndrome (DMC), a rare autosomal recessive disorder, is characterized by microcephaly, short trunk dwarfism and sometime psychomotor retardation. Cutaneous cells of affected individuals show dilated rough endoplasmic reticulum and enlarged vacuoles. The Dyggve-Melchior-Clausen syndrome protein, also designated dymeclin, may play a role in proteoglycan metabolism and intracellular protein digestion. It is a widely expressed multi-pass membrane protein, detected primarily in chondrocytes and fetal brain tissue. Defects in dymeclin are also the cause of Smith-McCort dysplasis syndrome (SMC), which has characteristics identical to those of Dyggve-Melchior-Clausen syndrome.

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Primary Antibodies

Catalog No. Host Iso. Clone Pres. React. Applications  

Dymeclin antibody

Detection limit for recombinant GST tagged DYM is approximately 1ng/ml as a capture antibody. Mouse IgG1 1C2 Purified Hu E
0.1 mg / €370.00
  Abnova Taiwan Corp.

Proteins & Growth Factors

Catalog No. Species Pres. Purity Source  

Dymeclin

Dymeclin Human > 80 %
Preparation: Recombint protein was captured through anti-DDK affinity column followed by conventiol chromatography steps.
Purity Detail: > 80% as determined by SDS-PAGE and Coomassie blue staining.
HEK293 cells
20 µg / €680.00
  OriGene Technologies, Inc.

Lysates

Catalog No.    

DYM overexpression lysate

DYM overexpression lysate  
0.1 mg / €280.00
  OriGene Technologies, Inc.

3 Item(s)

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