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Recombinant Human Jagged 1/JAG1 Protein (Fc Tag)– MSE Supplies LLC

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Recombinant Human Jagged 1/JAG1 Protein (Fc Tag)

SKU: PKSH033359-50

  • £39200
  • Save £4400



Recombinant Human Jagged 1/JAG1 Protein (Fc Tag)

 

SKU # PKSH033359
Expression Host HEK293 Cells

 

 

Description

Synonyms AGS, AHD, AWS, HJ1, JAG1 and CD339, JAGL1, Jagged 1, Jagged-1, Protein jagged-1 I
Species Human
Expression Host HEK293 Cells
Sequence Gln34-Ser1046
Accession P78504
Calculated Molecular Weight 137.6 kDa
Observed Molecular Weight 140-200 kDa
Tag C-Fc
Bio-activity Not validated for activity
  

 

Properties

Purity > 90 % as determined by reducing SDS-PAGE.
Endotoxin < 1.0 EU per μg of the protein as determined by the LAL method.
Storage Generally, lyophilized proteins are stable for up to 12 months when stored at -20 to -80℃. Reconstituted protein solution can be stored at 4-8℃ for 2-7 days. Aliquots of reconstituted samples are stable at < -20℃ for 3 months.
Shipping This product is provided as lyophilized powder which is shipped with ice packs.
Formulation Lyophilized from a 0.2 μm filtered solution of PBS, pH 7.4.
Normally 5% - 8% trehalose, mannitol and 0.01% Tween 80 are added as protectants before lyophilization.
Please refer to the specific buffer information in the printed manual.
Reconstitution Please refer to the printed manual for detailed information.



Background

Protein jagged-1 I, also known as Jagged-1, JAGL1, HJ1, JAG1 and CD339, is a single-pass type I membrane protein. JAG1 contains one DSL domain and sixteen EGF-like domain. JAG1 acts as a ligand for multiple Notch receptors and is involved in the mediation of Notch signaling. JAG1 may participate in early and late stages of mammalian cardiovascular development, JAG1 inhibits myoblast differentiation and enhances fibroblast growth factor-induced angiogenesis. Defects in JAG1 are the cause of Alagille syndrome type 1, which is autosomal dominant multisystem disorder defined clinically by hepatic bile duct paucity and cholestasis in association with cardiac, skeletal, and ophthalmologic manifestations.