MYOZ3
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Official Full Name
myozenin 3 -
Overview
Sclerostin is a protein that in humans is encoded by the SOST gene. Sclerostin is a secreted glycoprotein with a C-terminal cysteine knot-like (CTCK) domain and sequence similarity to the DAN (differential screening-selected gene aberrative in neuroblastoma) family of bone morphogenetic protein (BMP) antagonists. Sclerostin is produced by the osteocyte and has anti-anabolic effects on bone formation. -
Synonyms
CS3;CS-3;FRP3;FRZB;myozenin 3;FATZ-related protein 3;calsarcin-3;myozenin-3
Recombinant Proteins
- Human
- Rhesus Macaque
- Rhesus macaque
- Chicken
- Zebrafish
- HEK293
- E.coli
- Mammalian Cells
- Human Cells
- In Vitro Cell Free System
- His
- GST
- Avi
- Fc
- Non
Involved Pathway
MYOZ3 involved in several pathways and played different roles in them. We selected most pathways MYOZ3 participated on our site, such as , which may be useful for your reference. Also, other proteins which involved in the same pathway with MYOZ3 were listed below. Creative BioMart supplied nearly all the proteins listed, you can search them on our site.
| Pathway Name | Pathway Related Protein |
|---|
Protein Function
MYOZ3 has several biochemical functions, for example, . Some of the functions are cooperated with other proteins, some of the functions could acted by MYOZ3 itself. We selected most functions MYOZ3 had, and list some proteins which have the same functions with MYOZ3. You can find most of the proteins on our site.
| Function | Related Protein |
|---|
Interacting Protein
MYOZ3 has direct interactions with proteins and molecules. Those interactions were detected by several methods such as yeast two hybrid, co-IP, pull-down and so on. We selected proteins and molecules interacted with MYOZ3 here. Most of them are supplied by our site. Hope this information will be useful for your research of MYOZ3.
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References
- Gueugneau, M; Coudy-Gandilhon, C; et al. Proteomics of muscle chronological ageing in post-menopausal women. BMC GENOMICS 15:-(2014).
- Titheradge, H; Togneri, F; et al. Axenfeld-Rieger syndrome: Further clinical and array delineation of four unrelated patients with a 4q25 microdeletion. AMERICAN JOURNAL OF MEDICAL GENETICS PART A 164:1695-1701(2014).
