| ELK.No | ES12844 |
| Product name | T132E rabbit pAb |
| Reactivity | Human; Mouse |
| Applications | WB |
| Other name | |
| Size | 50μL |
| Unit price ($) | 148 |
| Human gene ID | 124842 |
| Human Swiss-Prot | Q6IEE7 |
| Source | Rabbit |
| Isotype | IgG |
| Target | T132E |
| Fields | |
| Gene name | TMEM132E |
| Protein name | T132E |
| Human gene link | View Human Gene |
| Human Swiss link | View Human Swiss-Prot |
| Mouse gene ID | 270893 |
| Mouse gene link | View Mouse Gene |
| Mouse Swiss-Prot | Q6IEE6 |
| Mouse Swiss link | View Mouse Swiss-Prot |
| Rat gene ID | |
| Rat gene link | |
| Rat Swiss-Prot | |
| Rat Swiss link | |
| Immunogen | Synthesized peptide derived from human T132E AA range: 486-536 |
| Specificity | This antibody detects endogenous levels of T132E at Human/Mouse |
| Formulation | Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide. |
| Clonality | Polyclonal |
| Dilution | WB 1:500-2000 |
| Purification | The antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen. |
| Concentration | 1 mg/ml |
| Storage stability | -20°C/1 year |
| Molecular Weight (Da) | 108kD |
| Observed band (KD) | |
| Background | |
| Function | disease:TMEM132E gene is identified as one gene located in a region involved in a heterozygous deletion of approximately 4.7 Mb; this deletion, involving the NF1 gene and contiguous genes lying in its flanking regions, is observed in one patient with NF1 and 17q11.2 microdeletion syndrome [MIM:162200]. The NF1 microdeletion syndrome is often characterized by a more severe phenotype than that observed in the majority of NF1 patients. Indeed, patients with NF1 microdeletion often show variable facial dysmorphism, mental retardation, developmental delay, and an excessive number of neurofibromas.,similarity:Belongs to the TMEM132 family., |
| Subcellular location | Membrane ; Single-pass type I membrane protein . |
| Expression |

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