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NXNL1


Official Full Name
nucleoredoxin like 1
Organism
Homo sapiens
Gene ID
115861
Background
Retinitis pigmentosa (RP) is a disease that leads to blindness by degeneration of cone photoreceptors. Rods produce factors required for cone viability. The protein encoded by this gene is one of those factors and is similar to a truncated form of thioredoxin. This gene has been proposed to have therapeutic value against RP. [provided by RefSeq, Dec 2015]
Synonyms
RDCVF; TXNL6

Cat.No. Product Name Price
SHH356768 shRNA set against Human NXNL1 (NM_138454.1) Inquiry
SHH356772 shRNA set against Mouse NXNL1 (NM_145598.2) Inquiry
SHW012098 shRNA set against Danio rerio NXNL1 (NM_001110760) Inquiry
Cat.No. Product Name Price
CDFG008087 Human NXNL1 cDNA Clone(NM_138454.1) Inquiry
MiUTR1H-10905 NXNL1 miRNA 3'UTR clone Inquiry
MiUTR1M-12348 NXNL1 miRNA 3'UTR clone Inquiry
CDCB173573 Danio rerio NXNL1 ORF Clone (NM_001110760) Inquiry
CDCR267531 Mouse Nxnl1 ORF Clone(NM_145598.2) Inquiry
CDCR316612 Human NXNL1 ORF Clone(NM_138454.1) Inquiry
CDCS416789 Human NXNL1 ORF Clone (BC014127) Inquiry
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