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Mouse DDR1 Kinase / MCK10 / CD167 Protein (GST Tag) PDF Download

Catalog Size (Price) Quantity In Stock Operation Other Information
50829-M20B1
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Protein Production & Purification Service

Discoidin domain receptor family, member 1 Protein Datasheet

 

DDR1 / CD167a Protein Price Inquiry ( Available Sizes )

DDR1 / CD167a Protein Product Information

Synonym : DDR1, Cak, Eddr1, Mpk6
Protein Construction: A DNA sequence encoding the mouse DDR1 (Q03146-2) (Leu444-Val874) was fused with the N-terminal polyhistidine-tagged GST tag at the N-terminus.
Source: Mouse
Expression Host: Baculovirus-Insect cells

DDR1 / CD167a Protein QC Testing

Purity: > 95 % as determined by SDS-PAGE SDS-PAGE:
SDS-PAGE

DDR1 / CD167a protein

Endotoxin: < 1.0 EU per μg of the protein as determined by the LAL method
Stability: Samples are stable for up to twelve months from date of receipt at -70℃
Predicted N terminal: Met
Molecular Mass:

The recombinant mouse DDR1/GST chimera consists of 668 amino acids and has a calculated molecular mass of 75.8kDa. The recombinant protein migrates as an approximately 68 kDa band in SDS-PAGE under reducing conditions.

Formulation: Lyophilized from sterile 20mM Tris, 500mM NaCl, pH 7.4, 10%glycerol, 2mM DTT.
  1. Normally 5 % - 8 % trehalose and mannitol are added as protectants before lyophilization. Specific concentrations are included in the hardcopy of COA.
  2. Please contact us for any concerns or special requirements.

DDR1 / CD167a Protein Usage Guide

Storage: Store it under sterile conditions at -70℃. It is recommended that the protein be aliquoted for optimal storage. Avoid repeated freeze-thaw cycles.
Reconstitution: A hardcopy of COA with reconstitution instruction is sent along with the products. Please refer to it for detailed information.

DDR1 / CD167a Protein Related Products & Topics

Related Areas:

Enzyme>>Protein Kinase>>Receptor Tyrosine Kinase>>DDR1/MCK10/CD167

Signal Transduction>>Protein Kinase>>Receptor Tyrosine Kinase>>DDR1/MCK10/CD167

Cancer>>Growth Factor & Receptor>>Receptor Tyrosine Kinase>>DDR1/MCK10/CD167

Immunology>>Cluster of Differentiation>>Other>>DDR1/MCK10/CD167

Proteins:

Molecule Species Description //For Detailed Info. and Price------CLICK! Cat. No
DDR1/MCK10/CD167 Human DDR1/MCK10/CD167 Protein, Recombinant 10730-H08H
DDR1/MCK10/CD167 Human DDR1 / CD167a (aa 444-913) Protein, Recombinant, with GST Tag 10730-H20B1
DDR1/MCK10/CD167 Mouse DDR1 / CD167a Protein, Recombinant 50829-M02H
DDR1/MCK10/CD167 Mouse DDR1/MCK10/CD167 Protein, Recombinant 50829-M08H
DDR1/MCK10/CD167 Mouse DDR1 / CD167a Protein, Recombinant, with GST Tag 50829-M020B1

Antibodies:

Molecule Application Description //For Detailed Info. and Price------CLICK! Cat. No
Human
DDR1/MCK10/CD167
WB, ELISA Rabbit Polyclonal Antibody 10730-RP01
Human
DDR1/MCK10/CD167
WB, ELISA DDR1/MCK10/CD167 Antibody, Rabbit Pab (Antigen Affinity Purified) 10730-RP02
Human
DDR1/MCK10/CD167
WB, ELISA DDR1 / CD167a Antibody 10730-MM05
Human
DDR1/MCK10/CD167
WB, ELISA DDR1 / CD167 Antibody 10730-R203

DDR1 / CD167a Protein Description

Mouse epithelial discoidin domain-containing receptor 1, also known as Tyrosine kinase DDR, Discoidin receptor tyrosine kinase, CD167a, and DDR1, is a single-pass type I membrane protein. It belongs to the protein kinase superfamily and Insulin receptor subfamily. DDR1 contains one?F5/8 type C domain and one protein kinase domain. DDR1 is expressed at low levels in most adult tissues and is highest in the brain, lung, placenta and kidney. Lower levels of expression are detected in melanocytes, heart, liver, skeletal muscle and pancreas. DDR1 is abundantly expressed in breast carcinoma cell lines. DDR1 regulates cell adhesion and a broad range of cell behavior. DDR1 plays an important role as a collagen receptor, mediating intimal thickening after vascular injury. DDR1 and DDR2 are tyrosine kinase receptors activated by triple-helical collagens. Aberrant expression and signaling of these receptors have been implicated in several human diseases linked to accelerated matrix degradation and remodeling including tumor invasion, atherosclerosis and liver fibrosis.

References

  1. Hou G. et al., 2001, J Clin Invest. 107 (6): 727-35.
  2. Abdulhussein R. et al., 2004, J Biol Chem. 279 (30): 31462-70.
  3. Mihai C. et al., 2009, J Mol Biol. 385 (2): 432-45.
  4. Wang CZ. et al., 2009, Am J Physiol Cell Physiol. 297 (2): C419-29.
  5. Flynn LA. et al., 2010, J Mol Biol. 395 (3): 533-43.