Description
Description
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
Sequence: QTSDQATLLLYTLLHQNSNIRTYMLARTDMENLVLPILEILYHVEERNSHHVYMALIILLILTEDDGFNRSIHEVILKNITWYSERVL
Specifications
| Antigen | dymeclin |
| Classification | Monoclonal |
| Conjugate | Unconjugated |
| Formulation | PBS with no preservative; pH 7.4 |
| Gene Accession No. | NM_017653 |
| Gene Symbols | DYM |
| Immunogen | DYM (NP_060123, 343 a.a. ∼ 430 a.a) partial recombinant protein with GST tag. MW of the GST tag alone is 26 KDa. |
| Quantity | 100 μg |
| Whole Molecule | Yes |
| Gene ID (Entrez) | 54808 |
| Content And Storage | Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing. |
| Isotype | IgG1 κ |
| Applications | ELISA |
| Clone | 1C2 |
| Description | Mouse monoclonal antibody raised against a partial recombinant DYM. |
| Gene | DYM |
| Gene Alias | DMC/FLJ20071/FLJ90130/SMC |
| Host Species | Mouse |
| Purification Method | Affinity Purified |
| Regulatory Status | RUO |
| Primary or Secondary | Primary |
| Target Species | Human |
| Product Type | Antibody |
