Background:

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.

Classification:

Primary antibody

Alternative names:

DYM

Species reactivity:

Human, Mouse, Rat

Host:

Rabbit

Isotype:

IgG

Immunogen:

Synthesized peptide derived from human DYM

Concentration:

1 mg/ml

Molecular weight:

73590

Applications:

WB

Storage:

-20°C for 1 year

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