Immobilized Recombinant Rat Jagged 1 (Catalog # 9907-JG) enhances Recombinant Human/Mouse/Rat BMP-2 Recombinant Human BMP‑2 (Catalog # 355-BM) alkaline phosphatase inducing activity in C3H10T1/2 mouse embryonic ...read more
2 μg/lane of Recombinant Rat Jagged 1 was resolved with SDS-PAGE under reducing (R) and non-reducing (NR) conditions and visualized by Coomassie® blue staining, showing bands at 134-160 kDa.
Recombinant Rat Jagged 1 His Tagged 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 0.4-2.4 μg/mL.
Source
Mouse myeloma cell line, NS0-derived rat Jagged 1 protein Ser32-Asp1067, with substitutions GGARN56-60AE and DR63-64TLVRPY and a C-terminal 6-His tag
>95%, 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
114 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
134-160 kDa, reducing conditions
Publications
Read Publication using 9907-JG in the following applications:
12 months from date of receipt, ≤ -20 °C as supplied.
1 month, 2 to 8 °C under sterile conditions after reconstitution.
3 months, ≤ -20 °C under sterile conditions after reconstitution.
Buffer
Lyophilized from a 0.2 μm filtered solution in PBS with Trehalose.
Purity
>95%, 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 Rat Jagged 1 His Tagged 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). 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 126 aa cytoplasmic domain. The large extracellular region
has a DSL (Delta, Serrate, Lag-2 consensus sequence) domain followed by
16 EGF-like repeats (2). Rat Jagged 1 shows 98% and 99% aa identity to
human and mouse Jagged 1 extracellular domains respectively. Relative to the
extracellular region of rat Jagged 2, the aa identity is 58%. The
extracellular region of Rat 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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