R3HCC1L Polyclonal Antibody

Rs. 16,500.00
SKU E-AB-16455


Synonyms C10orf28,C10orf28 protein,Chromosome 10 open reading frame 28,FLJ25458,FLJ37160,GIDRP86,GIDRP88,Growth inhibition and differentiation related protein 86,Growth inhibition and differentiation-related protein 88,PSORT,Putative mitochondrial space protein 32.1,R3H and coiled-coil domain-containing protein 1-like,R3H domain and coiled coil containing 1 like,R3HCC1L,R3HCL
Swissprot Q7Z5L2
Source Rabbit
Reactivity Human,Mouse
Immunogen Synthetic peptide of human R3HCC1L
Application IHC,ELISA
Recommended dilution IHC 1:50-1:200
Concentration 0.7mg/mL
Clonality Polyclonal


Cellular localization  
Tissue specificity  
Isotype IgG
Purification Affinity purification
Conjugation Unconjugated
Storage instructions Store at -20℃. Avoid freeze / thaw cycles.
Storage buffer PBS with 0.05% sodium azide, 50% glycerol, PH7.3
Background C10orf28 (chromosome 10 open reading frame 28), also known as GIDRP88 (growth inhibition and differentiation-related protein 88) or putative mitochondrial space protein 32.1, is a 792 amino acid protein that exists as three alternatively spliced isoforms. The gene encoding C10orf28 maps to human chromosome 10, which spans nearly 135 million base pairs, 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.


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