Datasheet
$199.00 – $429.00
Description
This gene is a paralog of SMN1 gene, which encodes the survival motor neuron protein, mutations in which are cause of autosomal recessive proximal spinal muscular atrophy. The protein encoded by this gene is a nuclear protein that has been identified as a constituent of the spliceosome complex. This gene is differentially expressed, with abundant levels in skeletal muscle, and may share similar cellular function as the SMN1 gene. [provided by RefSeq, Jul 2008].
Bioinformatics
| Weight | 1 lbs |
|---|---|
| Size | 20ug Purified Ab with BSA and Azide at 200ug/ml, 100ug, 100ug Purified Ab with BSA and Azide at 200ug/ml |
| Application | IHC |
| Symbol | SMNDC1 |
| Isotype | Mouse / IgG |
| Synonyms | SMNR, SPF30, TDRD16C |
| Entrez Gene ID | 10285 |
| UniProt | O75940 |
| Clone | PCRP-SMNDC1-1A8 |
| Supplied As | 200ug/ml of recombinant mAb Purified by Protein A/G. Prepared in 10mM PBS with 0.05% BSA & 0.05% azide. Also available WITHOUT BSA & azide at 1.0mg/ml. |
| Storage and Stability | Antibody with azide – store at 2 to 8°C. Antibody without azide – store at -20 to -80°C. Antibody is stable for 24 months. Non-hazardous. No MSDS required. |
| Categories | Cell Biology, Neurosciences, Transcription Factors |
Additional Information
| Storage and Stability |
Antibody with azide - store at 2 to 8°C. Antibody without azide - store at -20 to -80°C. Antibody is stable for 24 months. Non-hazardous. No MSDS required. |
|---|---|
| Supplied As |
200ug/ml of Ab Purified from Bioreactor Concentrate by Protein A/G. Prepared in 10mM PBS with 0.05% BSA & 0.05% azide. Also available WITHOUT BSA & azide at 1.0mg/ml. |
| Limitations |
This antibody is available for research use only and is not approved for use in diagnosis. |
| Warranty |
There are no warranties, expressed or implied, which extend beyond this description. Company is not liable for any personal injury or economic loss resulting from this product. |
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