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C10orf28 (D-14) Anticorpo: sc-138850

 |  Scheda tecnica
  • rabbit polyclonal IgG, 100 µg/ml
  • epitope mapping near the C-terminus of C10orf28 of human origin
  • recommended for detection of C10orf28 of human origin and D19Ertd386e of mouse origin of mouse, rat and human origin by WB, IF and ELISA; non cross-reactive with other C10orf family members ; also reactive with additional species, including equine, canine and bovine
  • blocking peptide, sc-138850 P
 
Altri C10orf28 Anticorpi ...
 
Informazioni ordini
Recommended Support Products:
(click button of application of choice)
WB   IF  
 
Specie Nome del gene Codice del gene Locus cromosoma Isoform (mRNA) Accession # codice accesso proteina Numero d'ordine
Umano C10orf28 27291 10q24.2 NM_014472 Q7Z5L2
n/a
Mouse D19Ertd386e 52013 19 C3 NM_177464 Q8BJM3
N/A
 
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 Informazioni ordini
Nome del prodottoCodice del prodottoUnitàPrezzoQuantitàAggiungiFavorites
C10orf28 (D-14) sc-138850 100 µg/ml $279
C10orf28 (D-14) P sc-138850 P
(peptide)
100 µg/0.5 ml $61

C10orf28 Background Information
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.