Immobilized Recombinant Mouse Jagged 1 Fc Chimera (Catalog # 10969-JG) enhances BMP-2 (355-BM) induced alkaline phosphatase activity in C3H10T1/2 mouse embryonic fibroblast cells. The ED50 for this effect is 1.00-6.00 ...read more
2 μg/lane of Recombinant Mouse Jagged 1 Fc Chimera Protein (Catalog # 10969-JG) was resolved with SDS-PAGE under reducing (R) and non-reducing (NR) conditions and visualized by Coomassie® Blue staining, showing ...read more
Recombinant Mouse Jagged 1 Fc Chimera Protein, CF Summary
Details of Functionality
Measured by the ability of the immobilized protein to enhance BMP-2 induced alkaline phosphatase activity in C3H10T1/2 mouse embryonic fibroblast cells. Nobta, M. et al. (2005) J. Biol. Chem. 280:15842. The ED50 for this effect is 1.00-6.00 μg/mL.
Source
Mouse myeloma cell line, NS0-derived mouse Jagged 1 protein
>90%, by SDS-PAGE visualized with Silver Staining and quantitative densitometry by Coomassie® Blue Staining.
Endotoxin Note
<0.10 EU per 1 μg of the protein by the LAL method.
Applications/Dilutions
Dilutions
Bioactivity
Theoretical MW
61 kDa. Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors.
SDS-PAGE
70-78 kDa, reducing conditions.
Publications
Read Publication using 10969-JG in the following applications:
Use a manual defrost freezer and avoid repeated freeze-thaw cycles.
12 months from date of receipt, -20 to -70 °C as supplied.
1 month, 2 to 8 °C under sterile conditions after reconstitution.
3 months, -20 to -70 °C under sterile conditions after reconstitution.
Buffer
Lyophilized from a 0.2 μm filtered solution in PBS.
Purity
>90%, by SDS-PAGE visualized with Silver Staining and quantitative densitometry by Coomassie® Blue Staining.
Reconstitution Instructions
Reconstitute at 500 μg/mL in PBS.
Notes
This product is produced by and ships from R&D Systems, Inc., a Bio-Techne brand.
Alternate Names for Recombinant Mouse Jagged 1 Fc Chimera Protein, CF
AGS
AHDMGC104644
Alagille syndrome
AWS
CD339 antigen
CD339
HJ1
JAG1
Jagged 1
Jagged1
JAGL1
protein jagged-1
Background
Jagged 1 is a 180 kDa type I transmembrane glycoprotein and member of the
Delta-Serrate-Lag-2 (DSL) family of ligands that activate LIN12/Notch proteins
(1). Mouse Jagged 1 is synthesized as a precursor protein that contains a 33 amino acid (aa)
signal sequence, a 1034 aa extracellular region, a 26 aa transmembrane (TM)
segment and a 125 aa cytoplasmic domain. The large extracellular region
has a DSL (Delta, Serrate, Lag-2 consensus sequence) domain followed by
16 EGF-like repeats (2). Mouse Jagged 1 shows 98% and 99% aa identity to
human and rat Jagged 1 extracellular domains respectively. The
extracellular region of Jagged 1 binds to multiple Notch receptors on the cell
surface as well as in solid phase binding studies. The DSL motif is necessary
for binding to Notch receptors and the EGF repeats modulate the affinity of the
interaction with Notch receptors (3). Notch signaling is implicated in many
developmental processes in a variety of cell types. Jagged-Notch signaling
specifies cell fate, regulates pattern formation, defines boundaries between
different cell types, and modulates cell proliferation and differentiation.
Some specific areas where Jagged is involved include hematopoiesis, myogenesis,
neurogenesis and development of the vasculature (4). For instance, soluble
non-transmembrane forms of Jagged1 influence behavior in fibroblast cells
leading to characteristics exhibited by endothelial cells during angiogenesis (5).
Soluble Jagged 1 is also capable of maintaining the survival and enhancing the
expansion of human stem cells that are capable of reconstituting hematopoietic
lineages in vivo (6). Furthermore, Jagged 1 is implicated in human
disease: Alagille syndrome, an autosomal dominant disorder characterized by
defects in liver, heart, eye, skeletal, craniofacial tissues, and kidney, is
caused by mutations in Jagged 1 (7). Depending on cell types and how soluble
forms of the ligand are presented, ligand binding can result in activation or
inhibition of Notch signaling (8).
Ascano, J. M. et al. (2003) J. Biol. Chem. 278:8771.
Lindsell, C.E. et al. (1995) Cell 80:909.
Shimizu, K. et al. (1999) J. Biol. Chem. 274:32961.
Lewis, J. (1998) Stem Cell & Dev. Biol. 9:583.
Small, D. et al. (2001) J. Biol. Chem. 276:32022.
Karanu, F. et al. (2000) J. Exp. Med. 192:1365.
Joutel, A. and E. Tounier-Lasserve (1998) Stem Cell & Dev. Biol. 9:619.
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