- Featured Product
- KD/KO Validated
SMN (Human-Specific) Monoklonaler Antikörper
SMN (Human-Specific) Monoklonal Antikörper für WB, IHC, IF/ICC, FC (Intra), IP, Indirect ELISA
Wirt / Isotyp
Maus / IgG2a
Getestete Reaktivität
human
Anwendung
WB, IHC, IF/ICC, FC (Intra), IP, Indirect ELISA
Konjugation
Unkonjugiert
CloneNo.
2C6D9
Kat-Nr. : 60154-1-PBS
Synonyme
Geprüfte Anwendungen
Produktinformation
60154-1-PBS bindet in WB, IHC, IF/ICC, FC (Intra), IP, Indirect ELISA SMN (Human-Specific) und zeigt Reaktivität mit human
Getestete Reaktivität | human |
Wirt / Isotyp | Maus / IgG2a |
Klonalität | Monoklonal |
Typ | Antikörper |
Immunogen | SMN (Human-Specific) fusion protein Ag14333 |
Vollständiger Name | survival of motor neuron 2, centromeric |
Berechnetes Molekulargewicht | 282 aa, 30 kDa |
Beobachtetes Molekulargewicht | 38 kDa |
GenBank-Zugangsnummer | BC000908 |
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
The survival of motor neurons (SMN) genes are the disease genes of spinal muscular atrophy (SMA), a common motor neuron degenerative disease. The level of SMN protein correlates with phenotypic severity of SMA. SMA patients lack a functional SMN1 gene, but they possess an intact SMN2 gene, which though nearly identical to SMN1, is only partially functional, because a large majority of SMN2 transcripts lack exon 7, resulting in production of a truncated, less stable SMN protein. This antibody 60154-1-Ig is specific to human SMN2. It can't recognize mouse and rat SMN.