SNX29 Antibody (PACO20573)
- SKU:
- PACO20573
- Product Type:
- Antibody
- Reactivity:
- Human
- Reactivity:
- Mouse
- Host Species:
- Rabbit
- Isotype:
- IgG
- Applications:
- ELISA
- Applications:
- IHC
- Antibody Type:
- Polyclonal Antibody
- Conjugation:
- Unconjugated
Description
| Antibody Name: | SNX29 Antibody (PACO20573) |
| Antibody SKU: | PACO20573 |
| Size: | 50ul |
| Host Species: | Rabbit |
| Tested Applications: | ELISA, IHC |
| Recommended Dilutions: | ELISA:1:1000-1:2000, IHC:1:25-1:100 |
| Species Reactivity: | Human, Mouse |
| Immunogen: | Synthetic peptide of human SNX29 |
| Form: | Liquid |
| Storage Buffer: | -20°C, pH7.4 PBS, 0.05% NaN3, 40% Glycerol |
| Purification Method: | Antigen affinity purification |
| Clonality: | Polyclonal |
| Isotype: | IgG |
| Conjugate: | Non-conjugated |
 | The image on the left is immunohistochemistry of paraffin-embedded Human colon cancer tissue using PACO20573(SNX29 Antibody) at dilution 1/30, on the right is treated with synthetic peptide. (Original magnification: x200). |
 | The image on the left is immunohistochemistry of paraffin-embedded Human liver cancer tissue using PACO20573(SNX29 Antibody) at dilution 1/30, on the right is treated with synthetic peptide. (Original magnification: x200). |
| Background: | 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. |
| Synonyms: | sorting nexin 29 |
| UniProt Protein Function: | SNX29: Belongs to the sorting nexin family. 2 isoforms of the human protein are produced by alternative splicing.Protein type: VesicleChromosomal Location of Human Ortholog: 16p13.13-p13.12 |
| UniProt Protein Details: | |
| NCBI Summary: | |
| UniProt Code: | Q8TEQ0 |
| NCBI GenInfo Identifier: | 353526314 |
| NCBI Gene ID: | 92017 |
| NCBI Accession: | Q8TEQ0.3 |
| UniProt Secondary Accession: | Q8TEQ0,Q8N2X2, Q9HA26, B5MDW2 |
| UniProt Related Accession: | Q8TEQ0 |
| Molecular Weight: | 89,144 Da |
| NCBI Full Name: | Sorting nexin-29 |
| NCBI Synonym Full Names: | sorting nexin 29 |
| NCBI Official Symbol: | SNX29 |
| NCBI Official Synonym Symbols: | RUNDC2A; A-388D4.1 |
| NCBI Protein Information: | sorting nexin-29 |
| UniProt Protein Name: | Sorting nexin-29 |
| UniProt Synonym Protein Names: | RUN domain-containing protein 2A |
| Protein Family: | Sorting nexin |
| UniProt Gene Name: | SNX29 |
| UniProt Entry Name: | SNX29_HUMAN |
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