TXNL6 Antibody (monoclonal) (M01)
Mouse monoclonal antibody raised against a partial recombinant NXNL1.
- SPECIFICATION
- CITATIONS
- PROTOCOLS
- BACKGROUND
Application
| WB |
---|---|
Primary Accession | Q96CM4 |
Other Accession | NM_138454 |
Reactivity | Human |
Host | mouse |
Clonality | Monoclonal |
Isotype | IgG2b Kappa |
Clone Names | 7H3 |
Calculated MW | 23943 Da |
Gene ID | 115861 |
---|---|
Other Names | Nucleoredoxin-like protein 1, Thioredoxin-like protein 6, NXNL1, TXNL6 |
Target/Specificity | NXNL1 (NP_612463, 81 a.a. ~ 190 a.a) partial recombinant protein with GST tag. MW of the GST tag alone is 26 KDa. |
Dilution | WB~~1:500~1000 |
Format | Clear, colorless solution in phosphate buffered saline, pH 7.2 . |
Storage | Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing. |
Precautions | TXNL6 Antibody (monoclonal) (M01) is for research use only and not for use in diagnostic or therapeutic procedures. |
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Provided below are standard protocols that you may find useful for product applications.
References
The homeobox gene CHX10/VSX2 regulates RdCVF promoter activity in the inner retina. Reichman S, et al. Hum Mol Genet, 2010 Jan 15. PMID 19843539.BBS7 and TTC8 (BBS8) mutations play a minor role in the mutational load of Bardet-Biedl syndrome in a multiethnic population. Bin J, et al. Hum Mutat, 2009 Jul. PMID 19402160.Thioredoxin-like 6 protects retinal cell line from photooxidative damage by upregulating NF-kappaB activity. Wang XW, et al. Free Radic Biol Med, 2008 Aug 1. PMID 18474255.Mapping of transcription start sites of human retina expressed genes. Roni V, et al. BMC Genomics, 2007 Feb 7. PMID 17286855.Disease-associated variants of the rod-derived cone viability factor (RdCVF) in Leber congenital amaurosis. Rod-derived cone viability variants in LCA. Hanein S, et al. Adv Exp Med Biol, 2006. PMID 17249548.
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