MATN1 polyclonal antibody
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More Files
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Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
Immunohistochemical staining (Formalin-fixed paraffin-embedded sections) of human skeletal muscle with MATN1 polyclonal antibody (Cat # PAB30991) shows moderate cytoplasmic positivity in myocytes.
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Specification
Product Description
Rabbit polyclonal antibody raised against partial recombinant human MATN1.
Immunogen
Recombinant protein corresponding to human MATN1.
Sequence
REIASEPVAEHYFYTADFKTINQIGKKLQKKICVEEDPCACESLVKFQAKVEGLLQALTRKLEAVSKRLAILENTVV
Host
Rabbit
Reactivity
Human
Form
Liquid
Purification
Antigen affinity purification
Isotype
IgG
Recommend Usage
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) (1:50-1:200)
The optimal working dilution should be determined by the end user.Storage Buffer
In PBS, pH 7.2 (40% glycerol, 0.02% sodium azide).
Storage Instruction
Store at 4°C. For long term storage store at -20°C.
Aliquot to avoid repeated freezing and thawing.Note
This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Applications
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
Immunohistochemical staining (Formalin-fixed paraffin-embedded sections) of human skeletal muscle with MATN1 polyclonal antibody (Cat # PAB30991) shows moderate cytoplasmic positivity in myocytes. -
Gene Info — MATN1
Entrez GeneID
4146Protein Accession#
P21941Gene Name
MATN1
Gene Alias
CMP, CRTM
Gene Description
matrilin 1, cartilage matrix protein
Omim ID
115437Gene Ontology
HyperlinkGene Summary
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. [provided by RefSeq
Other Designations
OTTHUMP00000003805|cartilage matrix protein
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Interactome
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Disease
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Publication Reference
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Loss of matrilin 1 does not exacerbate the skeletal phenotype in a mouse model of multiple epiphyseal dysplasia caused by a Matn3 V194D mutation.
Bell PA, Piróg KA, Fresquet M, Thornton DJ, Boot-Handford RP, Briggs MD.
Arthritis and Rheumatism 2012 May; 64(5):1529.
Application：IHC, WB-Ce, Mouse, Mouse chondrocytes, Mouse limbs.
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Loss of matrilin 1 does not exacerbate the skeletal phenotype in a mouse model of multiple epiphyseal dysplasia caused by a Matn3 V194D mutation.
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