DCN Antibody
Purified Mouse Monoclonal Antibody
- SPECIFICATION
- CITATIONS
- PROTOCOLS
- BACKGROUND
Application
| WB, E |
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Primary Accession | P07585 |
Reactivity | Human |
Host | Mouse |
Clonality | Monoclonal |
Clone Names | 1G4C5 |
Isotype | IgG1 |
Calculated MW | 39.7kDa |
Description | The protein encoded by this gene is a small cellular or pericellular matrix proteoglycan that is closely related in structure to biglycan protein. The encoded protein and biglycan are thought to be the result of a gene duplication. This protein is a component of connective tissue, binds to type I collagen fibrils, and plays a role in matrix assembly. It contains one attached glycosaminoglycan chain. This protein is capable of suppressing the growth of various tumor cell lines. There are multiple alternatively spliced transcript variants known for this gene. This gene is a candidate gene for Marfan syndrome. |
Immunogen | Purified recombinant fragment of human DCN (AA: 263-324) expressed in E. Coli. |
Formulation | Purified antibody in PBS with 0.05% sodium azide |
Gene ID | 1634 |
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Other Names | Decorin, Bone proteoglycan II, PG-S2, PG40, DCN, SLRR1B |
Dilution | E~~1/10000 WB~~1/500 - 1/2000 |
Storage | Maintain refrigerated at 2-8°C for up to 6 months. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles. |
Precautions | DCN Antibody is for research use only and not for use in diagnostic or therapeutic procedures. |
Name | DCN |
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Synonyms | SLRR1B |
Function | May affect the rate of fibrils formation. |
Cellular Location | Secreted, extracellular space, extracellular matrix. Secreted |
Tissue Location | Detected in placenta (at protein level) (PubMed:32337544). Detected in cerebrospinal fluid, fibroblasts and urine (at protein level) (PubMed:25326458, PubMed:36213313, PubMed:37453717). |
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Provided below are standard protocols that you may find useful for product applications.
Background
DNA (cytosine-5-)-methyltransferase 1 has a role in the establishment and regulation of tissue-specific patterns of methylated cytosine residues. Aberrant methylation patterns are associated with certain human tumors and developmental abnormalities. Two transcript variants encoding different isoforms have been found for this gene. ; ;
References
1. PLoS One. 2012;7(9):e45559. 2. Hum Reprod. 2012 Nov;27(11):3249-58.
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