Mouse Osteomodulin (OMD) Protein

Este producto es parte de OMD - Osteomodulin
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1079€ (100 µg)

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935106861
info@markelab.com
name
Mouse Osteomodulin (OMD) Protein
category
Proteins and Peptides
provider
Abbexa
reference
abx691970
tested applications
SDS-PAGE

Description

Mouse Osteomodulin Protein is a recombinant protein from Mouse produced in HEK293 Cells. A DNA sequence encoding the mouse OMD (NP_036180.1) (Met 1-Ile 423) precusor was expressed, with a C-terminal polyhistidine tag.

Documents del producto

Instrucciones
Data sheet
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Product specifications

Category
Proteins and Peptides
Immunogen Target
Osteomodulin
Host
HEK293 cells
Origin
Mouse
Observed MW
Molecular Weight: 48.8 kDa
Sequence Fragment: Met1-Ile423
Tag: C-terminal His tag
Validity: The validity for this protein is 12 months.
Expression
Recombinant
Purity
> 96% (SDS-PAGE)
Size 1
100 µg
Form
 
Tested Applications
SDS-PAGE
Buffer
Lyophilized from sterile PBS, pH 7.4.
Availability
Shipped within 5-15 working days.
Storage
Aliquot and store at -20°C or -80°C. Avoid repeated freeze/thaw cycles.
Dry Ice
No
UniProt ID
O35103
NCBI Accession
NP_036180.1
Alias
OSAD,SLRR2C,KSPG osteomodulin,Osteoadherin
Background
Protein OMD
Status
RUO
Note
This product is for research use only.   Not for human consumption, cosmetic, therapeutic or diagnostic use.

Descripción

Osteomodulin (OMD) is a small leucine-rich proteoglycan primarily expressed in the bone and cartilage, where it plays a key role in regulating extracellular matrix (ECM) structure and function OMD is involved in bone mineralization, collagen fibril organization, and cartilage development by interacting with collagen and other ECM components It contributes to skeletal integrity and has a significant impact on the mechanical properties of bone, influencing bone strength and elasticity OMD’s expression is upregulated during bone remodeling, and its role in cartilage integrity makes it crucial for joint health and skeletal repair Dysregulation of OMD expression has been associated with bone diseases such as osteogenesis imperfecta and osteoarthritis, where altered ECM composition leads to skeletal deformities and joint degradation Studies also suggest that OMD influences cell signaling pathways, particularly those related to osteoblast differentiation and function, highlighting its broader role in skeletal development and disease

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