epitope corresponding to amino acids 1-143 representing full length Opalin of mouse origin
Modification Notes
Opalin, also known as HTMP10, oligodendrocytic myelin paranodal and inner loop protein or TMEM10 (transmembrane protein 10), is a 141 amino acid single-pass type I membrane protein that is expressed specifically in oligodendrocytes of brain. The gene encoding Opalin maps to human chromosome 10q24.1.Spanning nearly 135 million base pairs, chromosome 10 makes up approximately 4.5% of total DNA in cells and encodes nearly 1,200 genes. Several protein-coding genes, including those that encode for chemokines, cadherins, excision repair proteins, early growth response factors (Egrs) and fibroblast growth receptors (FGFRs), are located on chromosome 10. Defects in some of the genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman’s syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria.
Key Feature
Clonality
Polyclonal
Isotype
IgG
Host Species
Rabbit
Tested Applications
WBIPIFELISA
recommended for detection of Opalin of mouse, rat and, to a lesser extent, human origin by WB, IP, IF and ELISA:
Species Reactivity
HumanMouseRat
Concentration
1mg/ml
Purification
Affinity purified
Target Information
Alternative Names
epitope corresponding to amino acids 1-143 representing full length Opalin of mouse origin
Tissue Specificity
epitope corresponding to amino acids 1-143 representing full length Opalin of mouse origin