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mutation of Nectin-4 has been correlated with ectodermal dysplasia-syndactyly syndrome
is a protein that in humans is encoded by the KRT20 gene
coli Molecular Weight 27 kDa (Reducing)
the reaction was added to the immediate TY for about 20min
application dilution species WB 1:1000 Hu ICC 1:500 ICC ICFCM 1:500 Hu
SLC25A51 Recombinant Rabbit mAb (S-2070-74) Drug Target Proteins mutation of Nectin-4 has beenProduct Specification Host Rabbit Antigen SLC25A51 Synonyms Mitochondrial nicotinamide adenine dinucleotide transporter SLC25A51; Mitochondrial NAD(+) transporter SLC25A51; Mitochondrial carrier triple repeat protein 1; Solute carrier family 25 member 51; MCART1 Immunogen Synthetic Peptide Location Mitochondrion Accession Q9H1U9 Clone Number S 2070 74 Antibody Type Recombinant mAb Isotype IgG Application WB, IHC P Reactivity Hu, Ms Positive Sample HT
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