Dymeclin Protein (DYM) (Myc-DYKDDDDK Tag)
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- Target See all Dymeclin (DYM) Proteins
- Dymeclin (DYM)
- Protein Type
- Recombinant
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Origin
- Human
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Source
- HEK-293 Cells
- Purification tag / Conjugate
- This Dymeclin protein is labelled with Myc-DYKDDDDK Tag.
- Application
- Antibody Production (AbP), Standard (STD)
- Characteristics
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- Recombinant human Dymeclin protein expressed in HEK293 cells.
- Produced with end-sequenced ORF clone
- Purity
- > 80 % as determined by SDS-PAGE and Coomassie blue staining
- Top Product
- Discover our top product DYM Protein
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Dymeclin (DYM) (AA 343-430) protein (GST tag)
DYM Origin: Human Host: Wheat germ Recombinant WB, ELISA, AA, AP
Dymeclin (DYM) (AA 2-669) protein (His tag)Crystallography grade DYM Origin: Human Host: Insect Cells Recombinant >95 % as determined by SDS PAGE, Size Exclusion Chromatography and Western Blot. WB, SDS, ELISA, Crys
Dymeclin (DYM) (AA 2-669) protein (His tag)Crystallography grade DYM Origin: Mouse Host: Insect Cells Recombinant >95 % as determined by SDS PAGE, Size Exclusion Chromatography and Western Blot. WB, SDS, ELISA, Crys
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- Application Notes
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Recombinant human proteins can be used for:
Native antigens for optimized antibody production
Positive controls in ELISA and other antibody assays - Comment
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The tag is located at the C-terminal.
- Restrictions
- For Research Use only
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- Concentration
- 50 μg/mL
- Buffer
- 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
- Storage
- -80 °C
- Storage Comment
- Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
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- Target
- Dymeclin (DYM)
- Alternative Name
- Dymeclin (DYM Products)
- Synonyms
- DYM Protein, LOC734107 Protein, dym Protein, DMC Protein, SMC Protein, 1810041M12Rik Protein, 4933427L07Rik Protein, C030019K18Rik Protein, RGD1309111 Protein, dymeclin Protein, dymeclin L homeolog Protein, DYM Protein, dym Protein, Dym Protein, dym.L Protein
- 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.
- Molecular Weight
- 75.8 kDa
- NCBI Accession
- NP_060123
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