SMN Rekombinanter Antikörper
SMN Rekombinant Antikörper für WB, IF/ICC, IP, Cytometric bead array, Sandwich ELISA, Indirect ELISA
Wirt / Isotyp
Kaninchen / IgG
Getestete Reaktivität
human, Maus, Ratte
Anwendung
WB, IF/ICC, IP, Cytometric bead array, Sandwich ELISA, Indirect ELISA
Konjugation
Unkonjugiert
CloneNo.
251620C4
Kat-Nr. : 86668-2-PBS
Synonyme
Geprüfte Anwendungen
Produktinformation
86668-2-PBS bindet in WB, IF/ICC, IP, Cytometric bead array, Sandwich ELISA, Indirect ELISA SMN und zeigt Reaktivität mit human, Maus, Ratten
| Getestete Reaktivität | human, Maus, Ratte |
| Wirt / Isotyp | Kaninchen / IgG |
| Klonalität | Rekombinant |
| Typ | Antikörper |
| Immunogen | SMN fusion protein Eg4812 |
| Vollständiger Name | survival of motor neuron 2, centromeric |
| Berechnetes Molekulargewicht | 30 kDa |
| Beobachtetes Molekulargewicht | 38 kDa |
| GenBank-Zugangsnummer | BC015308 |
| Gene symbol | SMN |
| Gene ID (NCBI) | 6607 |
| Konjugation | Unkonjugiert |
| Form | Liquid |
| Reinigungsmethode | Protein-A-Reinigung |
| Lagerungspuffer | PBS only |
| Lagerungsbedingungen | Store at -80°C. 20ul Größen enthalten 0,1% BSA. |
Hintergrundinformationen
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.















