Noggin Recombinant

Catalog #
90256-2
$375 *
Size: 20 µg
Qty
*US Pricing only. For international pricing, please contact your local distributor.
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Description

Human Noggin, also known as symphalangism 1 (SYM1) or synostoses (multiple) syndrome 1 (SYNS1), GenBank Accession No. NM_005450, a.a. 28-232(end), disulfide-linked homodimer. MW=~28kDa (monomer). Source: human 293 cells. Endotoxin Level: <1 EU/μg. Biological Activity: measured by Noggin’s ability to inhibit BMP-4-induced alkaline phosphatase production by C2C12 mouse myoblast cells. The ED50 is < 20 ng/ml in the presence of 30 ng/ml of human BMP-4. Formulation: Lyophilized from a 0.2 μM filtered, aqueous solution. Reconstitution: Supplied as a lyophilized solid. Reconstitute in sterile water with 0.1% BSA to a final concentration of 0.1 mg/ml. Final formulation will be 50 mM Tris, pH 8.0, 1.2 M NaCl, 2.7 mM KCl, 0.1% BSA.

Synonyms
Noggin, symphalangism 1, SYM1, synostoses (multiple) syndrome 1, SYNS1
Product Info
Storage and Usage
Citations
Species
Human
Host Species/Expression System
FreeStyle 293-F cells
Format
Lyophilized solid
Formulation
Lyophilized from a 0.2 µm filtered 0.1 mg/ml solution of 50 mM Tris, pH 8.0, 1.2 M NaCl, 2.7 mM KCl, 0.1% BSA
MW
28 kDa
Endotoxin Level
< 1EU per µg of Noggin as determined by the LAL method.
Amino Acids
28–232(end)
Biological Activity
Measured by Noggin’s ability to inhibit BMP-4-induced alkaline phosphatase production by C2C12 mouse myoblast cells. The ED50 is <20 ng/ml in the presence of 30 ng/ml of human BMP-4.
Genbank #
NM_005450
UniProt #
Q13253
Tag(s)
none
Background
Noggin is one of a group of proteins that act as secreted antagonists of BMP activity. BMPs are essential for osteogenesis and organogenesis during embryonic development, and also play a role in tissue healing in adults. Noggin inhibits BMP activity by binding to them with high affinity, blocking their ability to bind to their receptor.
References
1. Tao, Y.X., et al. (2010). Indian J. Exp. Biol. 48(5):444-52.
2. Mfopou, J.K., et al. (2010). Gastroenterology. 138(7):2233- 2245.
3. Chaturvedi, G., et al. (2009). Cell Prolif. 42(4):425-33