SMN-Exon7 Monoclonal antibody
SMN-Exon7 Monoclonal Antibody for IF/ICC, WB,ELISA
Host / Isotype
Mouse / IgG1
Reactivity
human
Applications
IF/ICC, WB,ELISA
Conjugate
Unconjugated
CloneNo.
3A8G11
验证数据展示
经过测试的应用
| Positive WB detected in | HEK-293 cells, HeLa cells, HepG2 cells |
| Positive IF detected in | HepG2 cells |
Planning an IF experiment? We recommend our CoraLite® Plus 488 and CoraLite®594 conjugated versions of this antibody.
推荐稀释比
| Application | Dilution |
|---|---|
| Western Blot (WB) | WB : 1:500-1:2000 |
| Immunofluorescence (IF) | IF : 1:50-1:500 |
| 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. | |
发表文章中的应用
| WB | See 1 publications below |
产品信息
The immunogen of 60255-1-Ig is SMN-Exon7 Fusion Protein expressed in E. coli.
| Tested Applications | IF/ICC, WB,ELISA |
| Cited Applications | WB |
| Tested Reactivity | human |
| Immunogen | SMN-Exon7 fusion protein Ag16615 种属同源性预测 |
| Host / Isotype | Mouse / IgG1 |
| Class | Monoclonal |
| Type | Antibody |
| Full Name | survival of motor neuron 1, telomeric |
| Synonyms | Component of gems 1, Gemin 1, SMN, SMN1, SMN2, SMNC, SMN-Exon7, SMNT, Survival motor neuron protein, T BCD541 |
| Calculated Molecular Weight | 294 aa, 32 kDa |
| Observed Molecular Weight | 40 kDa |
| GenBank Accession Number | BC062723 |
| Gene Symbol | SMN1 |
| Gene ID (NCBI) | 6606 |
| RRID | AB_2881376 |
| Conjugate | Unconjugated |
| Form | Liquid |
| Purification Method | Protein A purification |
| UNIPROT ID | Q16637 |
| 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
Spinal muscular atrophy (SMA) is an autosomal recessive neurodegenerative disease characterized by loss of anterior horn cells in the spinal cord and concomitant symmetrical muscle weakness and atrophy (PMID: 16364894 ). SMA is caused by deletion or mutations of the survival motor neuron (SMN1) gene. SMA patients lack a functional SMN1 gene, but they possess an intact SMN2 gene, which though nearly identical to SMN1, is only partially functional (PMID: 17355180). A large majority of SMN2 transcripts lack exon 7, resulting in production of a truncated, less stable SMN protein (PMID: 10369862). The level of SMN protein correlates with phenotypic severity of SMA. This antibody, 60255-1-Ig, raised against the C-terminal region (275-294aa) encoded by the exon 7.
实验方案
| Product Specific Protocols | |
|---|---|
| WB protocol for SMN-Exon7 antibody 60255-1-Ig | Download protocol |
| IF protocol for SMN-Exon7 antibody 60255-1-Ig | Download protocol |
| Standard Protocols | |
|---|---|
| Click here to view our Standard Protocols |
发表文章
| Species | Application | Title |
|---|---|---|
