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E-AB-16455

R3HCC1L Polyclonal Antibody

Größe

£106.20

War £118.00

SKU:
E-AB-16455
Zusätzliche Namen:
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
Anwendung:
IHC
Konzentration:
0.7 mg/ml
Aufreinigung:
Affinity Purified
Lagerbedingungen:
-20[o]C Avoid freeze/thaw cycles.
Hersteller:
Elabscience
Host:
Rabbit
Reaktivitäten:
Human, Mouse
Buffer:
Phosphate buffered solution, pH 7.4, containing 0.05% stabilizer and 50% glycerol.
Immunogen:
Synthetic peptide of human R3HCC1L
Uniprot:
Q7Z5L2
Synonyme:
C10orf28;coiled-coil domain-containing protein R3HCC1L;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
Weitere Details:
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.
Versandbedingungen:
Blue Ice