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MATN1 Antibody (C-term)
Affinity Purified Rabbit Polyclonal Antibody (Pab)
- SPECIFICATION
- CITATIONS
- PROTOCOLS
- BACKGROUND
Application 
| IHC-P, WB, E |
|---|---|
| Primary Accession | P21941 |
| Other Accession | NP_002370.1 |
| Reactivity | Human |
| Host | Rabbit |
| Clonality | Polyclonal |
| Isotype | Rabbit IgG |
| Calculated MW | 53701 Da |
| Antigen Region | 376-405 aa |
| Gene ID | 4146 |
|---|---|
| Other Names | Cartilage matrix protein, Matrilin-1, MATN1, CMP, CRTM |
| Target/Specificity | This MATN1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 376-405 amino acids from the C-terminal region of human MATN1. |
| Dilution | WB~~1:1000 IHC-P~~1:10~50 |
| Format | Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein A column, followed by peptide affinity purification. |
| Storage | Maintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles. |
| Precautions | MATN1 Antibody (C-term) is for research use only and not for use in diagnostic or therapeutic procedures. |
| Name | MATN1 |
|---|---|
| Synonyms | CMP, CRTM |
| Function | Cartilage matrix protein is a major component of the extracellular matrix of non-articular cartilage. It binds to collagen. |
| Cellular Location | Secreted, extracellular space, extracellular matrix |
Thousands of laboratories across the world have published research that depended on the performance of antibodies from Abcepta to advance their research. Check out links to articles that cite our products in major peer-reviewed journals, organized by research category.
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Provided below are standard protocols that you may find useful for product applications.
Background
This gene encodes a member of von Willebrand factor A domain containing protein family. This family of proteins are thought to be involved in the formation of filamentous networks in the extracellular matrices of various tissues. Mutations of this gene have been associated with variety of inherited chondrodysplasias.
References
Jang, J.Y., et al. J. Dent. Res. 89(11):1203-1207(2010)
Fresquet, M., et al. J. Biol. Chem. 285(44):34048-34061(2010)
Wheeler, H.E., et al. PLoS Genet. 5 (10), E1000685 (2009) :
Chen, Z.J., et al. Zhonghua Wai Ke Za Zhi 47(17):1332-1335(2009)
Caporaso, N., et al. PLoS ONE 4 (2), E4653 (2009) :
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