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Cynomolgus EphB6 / EPHB6 Protein

Sino Biological Inc. liefert Cynomolgus EphB6 / EPHB6 Protein mit höherer Qualität und günstiger Kosten im Vergleich mit anderen globalen Lieferanten.

Weitere Informationen über Cynomolgus EphB6 / EPHB6 Protein lesen Sie bitte: http://www.sinobiological.com/EphB6-EPHB6-Protein-g-10012.html

Produkt-Information von EphB6 / EPHB6 Protein

Synonym EPHB6
Protein Construction

A DNA sequence encoding the cynomolgus EPHB6 (Met1-Ser591) was expressed, fused with the Fc region of human IgG1 at the C-terminus.

Source Cynomolgus
Expression Host Human Cells

QC Testing von EphB6 / EPHB6 Protein

Purity > 85 % as determined by SDS-PAGE SDS-PAGE:
SDS-PAGE

EphB6 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 Leu 32
Molecular Mass

The recombinant cynomolgus EPHB6 is a disulfide-linked homodimer. The reduced monomer comprises 801 amino acids and has a calculated molecular mass of 86.9 KDa.The apparent molecular mass of the protein is approximately 97 KDa respectively in SDS-PAGE.

Formulation Lyophilized from sterile PBS, pH7.4.
  1. Normally 5 % - 8 % trehalose and mannitol are added as protectants before lyophilization. Specific concentrations are included in the hardcopy of COA.

Usage Guide von EphB6 / EPHB6 Protein

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.

Verwandte Produkte & Themen von EphB6 / EPHB6 Protein

Related Areas:

Enzyme>>Protein Kinase>>Receptor Tyrosine Kinase>>EphB6

Neuroscience>>Axon Guidance>>Ephrin & Eph Receptor>>EphB6

Signal Transduction>>Protein Kinase>>Receptor Tyrosine Kinase>>EphB6

Cancer>>Growth Factor & Receptor>>Ephrin & Eph Receptor>>EphB6

Cancer>>Growth Factor & Receptor>>Receptor Tyrosine Kinase>>EphB6

Immunology>>Adaptive Immunity>>Costimulation & Costimulatory Molecule>>EphB6

Proteins:
Molecule Species Description //For Detailed Info. and Price------CLICK! Cat. No
EphB6 Human EphB6/Fc Protein, Recombinant 10197-H02H
EphB6 Human EphB6 Protein, Recombinant 10197-H08H
EphB6 Human EphB6 Protein, Recombinant 10197-HCCH
EphB6 Cynomolgus EphB6 / EPHB6 Protein, Recombinant 90045-C02H
Antibodies:
Molecule Application Description //For Detailed Info. and Price------CLICK! Cat. No
Human
EphB6
FCM EphB6 Antibody ( FITC ) 10197-MM05-F
Human
EphB6
WB, ELISA EphB6 Antibody, Mouse MAb 10197-MM07
Human
EphB6
WB, ELISA EphB6 Antibody, Rabbit PAb 10197-RP01
Human
EphB6
WB, ELISA EphB6 Antibody, Rabbit PAb (Antigen Affinity Purified) 10197-RP02

Beschreibung von EphB6 / EPHB6 Protein

Ephrins are divided into the ephrin-A (EFNA) class and the ephrin-B (EFNB) class based on their structures and sequence relationships. Ephrin receptors make up the largest subgroup of the receptor tyrosine kinase (RTK) family, and EphB6 binding to ephrin-B ligands is a unique member in that its kinase domain contains several alterations in conserved amino acids and is catalytically inactive. It is indicated that activated by an Src family kinase, EphB6 can act as both positive and negative regulators in the process of cell adhesion and migration,The large family of Ephrin receptors and their ligands , the ephrins , mediate numerous developmental processes, particularly the establishment of regional pattern in the nervous system. Furthermore, the Eph receptors have been suggested to play important roles in tumor formation, prognosis, and possible gene-therapeutic approaches, and the reduction of EphB6 gene expression is associated with the progression of metastatic diseases.

References

  1. Flanagan JG. et al., 1998, Annu Rev Neurosci. 21: 309-45.
  2. Matsuoka H. et al., 2005, J Biol Chem. 280: 29355-63.
  3. Holder N. et al., 1999, Development. 126: 2033-44.
  4. Cheng N. et al., 2002, Cytokine Growth Factor Rev. 13: 75-85.
  5. Hafner C. et al., 2003, Int J Oncol. 23: 1553-9.
  6. Fox BP. et al., 2006, Biochem Biophys Res Commun.340: 268-76.
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