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Invitrogen™ NUP210L Polyclonal Antibody

Rabbit Polyclonal Antibody
Brand: Invitrogen™ PA5115678
This item is not returnable.
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Description
Antibody detects endogenous levels of total NUP210L.
Nup210L (nuclear pore membrane glycoprotein 210-like) is a 1,888 amino acid single-pass membrane protein that belongs to the NUP210 family. The gene that encodes Nup210L consists of approximately 162,432 bases and maps to human chromosome 1q21.3. Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1.
Specifications
| NUP210L | |
| Polyclonal | |
| Unconjugated | |
| NUP210L | |
| Nuclear pore membrane glycoprotein 210-like; nuclear pore membrane glycoprotein 210-like (LOC91181); Nucleoporin 210 kDa-like; nucleoporin 210 like; nucleoporin 210kDa like; nucleoporin 210kDa-like; nucleoporin 210-like; nucleoporin Nup210-like; NUP210L; RGD1310250 | |
| Rabbit | |
| Affinity Chromatography | |
| RUO | |
| 91181 | |
| -20°C | |
| Liquid |
| Western Blot | |
| 1 mg/mL | |
| PBS with 50% glycerol and 0.02% sodium azide | |
| Q5VU65 | |
| NUP210L | |
| A synthesized peptide derived from human NUP210L(Accession Q5VU65), corresponding to amino acid residues N1016-D1066. | |
| 100 μL | |
| Primary | |
| Human | |
| Antibody | |
| IgG |
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