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Invitrogen™ SNX29 Polyclonal Antibody
Rabbit Polyclonal Antibody
Brand: Invitrogen™ PA550771
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Description
The antibody detects endogenous levels of total RUNDC2A protein.
SNX29 also known as RUNDC2A, is a 375 amino protein that contains one RUN domain. RUNDC2A is encoded by a gene that maps to human chromosome 16p13.13, which encodes over 900 genes and comprises nearly 3% of the human genome. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, as is Crohn's disease, which is a gastrointestinal inflammatory condition.
Specifications
| SNX29 | |
| Polyclonal | |
| Unconjugated | |
| SNX29 | |
| 4933437K13Rik; A-388D4.1; ENSMUSG00000079738; Gm11170; Gm1737; Gm930; RUN domain containing 2A; RUN domain-containing protein 2A; RUNDC2A; SNX29; SODD; sorting nexin 29; sorting nexin-29 | |
| Rabbit | |
| Antigen Affinity Chromatography | |
| RUO | |
| 92017 | |
| -20°C | |
| Liquid |
| Immunohistochemistry (Paraffin) | |
| 1.1 mg/mL | |
| PBS with 40% glycerol and 0.05% sodium azide; pH 7.4 | |
| Q8TEQ0 | |
| SNX29 | |
| Synthetic peptide corresponding to residues near the C terminal of human sorting nexin 29. | |
| 100 μL | |
| Primary | |
| Human | |
| Antibody | |
| IgG |
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