验证数据展示
经过测试的应用
| Positive WB detected in | A431 cells, Y79 cells, rat retina tissue |
| Positive IF/ICC detected in | Y79 cells |
推荐稀释比
| Application | Dilution |
|---|---|
| Western Blot (WB) | WB : 1:500-1:2000 |
| Immunofluorescence (IF)/ICC | IF/ICC : 1:125-1:500 |
| It is recommended that this reagent should be titrated in each testing system to obtain optimal results. | |
| Sample-dependent, Check data in validation data gallery. | |
产品信息
83807-1-RR targets MYO7A in WB, IF/ICC, ELISA applications and shows reactivity with human, rat samples.
| Tested Applications | WB, IF/ICC, ELISA Application Description |
| Tested Reactivity | human, rat |
| Immunogen | Peptide 种属同源性预测 |
| Host / Isotype | Rabbit / IgG |
| Class | Recombinant |
| Type | Antibody |
| Full Name | myosin VIIA |
| Synonyms | MYU7A, MYOVIIA, myosin VIIA, DFNB2, DFNA11 |
| Calculated Molecular Weight | 254 kDa |
| Observed Molecular Weight | 254 kDa |
| GenBank Accession Number | NM_000260 |
| Gene Symbol | MYO7A |
| Gene ID (NCBI) | 4647 |
| RRID | AB_3671394 |
| Conjugate | Unconjugated |
| Form | Liquid |
| Purification Method | Protein A purfication |
| UNIPROT ID | Q13402 |
| Storage Buffer | PBS with 0.02% sodium azide and 50% glycerol pH 7.3. |
| Storage Conditions | Store at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage. |
背景介绍
MYO7A, also named a USH1B, is one of myosins protein which are actin-based motor molecules with ATPase activity. Unconventional myosins serve in intracellular movements. Their highly divergent tails are presumed to bind to membranous compartments, which would be moved relative to actin filaments. In retina, MYO7A might play a role in trafficking of ribbon-synaptic vesicle complexes and renewal of the outer photoreceptors disks. In inner ear, it might maintain the rigidity of stereocilia during the dynamic movements of the bundle. It is involved in hair-cell vesicle trafficking of aminoglycosides, which are known to induce ototoxicity. Defects in MYO7A are the cause of Usher syndrome type 1B (USH1B). Defects in MYO7A are the cause of deafness autosomal recessive type 2 (DFNB2). Defects in MYO7A are the cause of deafness autosomal dominant type 11 (DFNA11). The antibody is specific to MYO7A.
实验方案
| Product Specific Protocols | |
|---|---|
| WB protocol for MYO7A antibody 83807-1-RR | Download protocol |
| IF protocol for MYO7A antibody 83807-1-RR | Download protocol |
| Standard Protocols | |
|---|---|
| Click here to view our Standard Protocols |