Recombinant Human Noggin Protein Summary
| Description |
A recombinant protein with a C-Terminal His-tag and corresponding to the amino acids 28-232 of Human Noggin Source:Baculovirus Amino Acid Sequence: QHYLHIRPAP SDNLPLVDLI EHPDPIFDPK EKDLNETLLR SLLGGHYDPG FMATSPPEDR PGGGGGAAGG AEDLAELDQL LRQRPSGAMP
SEIKGLEFSE GLAQGKKQRL SKKLRRKLQM WLWSQTFCPV LYAWNDLGSR FWPRYVKVGS CFSKRSCSVP EGMVCKPSKS VHLTVLRWRC
QRRGGQRCGW IPIQYPIISE CKCSCHHHHH H |
| Source |
Baculovirus |
| Protein/Peptide Type |
Recombinant Protein |
| Gene |
NOG |
| Purity |
>90%, by SDS-PAGE |
| Endotoxin Note |
< 1.0 EU per 1 microgram of protein (determined by LAL method) |
Applications/Dilutions
| Dilutions |
|
| Theoretical MW |
23.8 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. |
Packaging, Storage & Formulations
| Storage |
Store at 4C short term. Aliquot and store at -20C long term. Avoid freeze-thaw cycles. |
| Buffer |
PBS (pH 7.4), 10% glycerol |
| Preservative |
No Preservative |
| Concentration |
0.25 mg/ml |
| Purity |
>90%, by SDS-PAGE |
Alternate Names for Recombinant Human Noggin Protein
Background
Noggin is involved in numerous developmental processes, such as neural tube fusion and joint formation. The morphogenesis of organs is initiated by a downgrowth from a layer of epithelial stem cells. This process is achieved through the receipt of signals from 1) a WNT protein (WNT3A) to stabilize beta-catenin; and 2) Noggin, which is a bone morphogenetic protein inhibitor. Noggin mutations in unrelated families with proximal symphalangism (SYM1) and multiple synostoses syndrome (SYNS1) have been identified, which have multiple joint fusion as their principal defect.
Limitations
This product is for research use only and is not approved for use in humans or in clinical diagnosis. Peptides and proteins are
guaranteed for 3 months from date of receipt.
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