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SMN1 Rabbit anti-Human, Polyclonal, Bethyl Laboratories
Rabbit Polyclonal Antibody
Supplier: Bethyl Laboratories, Inc A301862AT
Description
The recommended shelf life for this product is 1 year from date of receipt.
The SMN1 gene is part of a 500 kb inverted duplication on chromosome 5q13. This duplicated region contains at least four genes and repetitive elements which make it prone to rearrangements and deletions. The repetitiveness and complexity of the sequence have also caused difficulty in determining the organization of this genomic region. The telomeric and centromeric copies of this gene are nearly identical and encode the same protein - survival motor neuron protein. The SMN complex plays a catalyst role in the assemble of small nuclear ribonucleoproteins, the building blocks of the spliceosome. Mutations in the SMN1 gene are known to cause spinal muscular atrophy 1/2.Specifications
| SMN1 | |
| Polyclonal | |
| Unconjugated | |
| SMN1 | |
| BCD541, SMA, SMA1, SMA2, SMA3, SMA4, SMA@, SMN, SMN2, SMNT, T-BCD541, component of gems 1; gemin 1; gemin-1; survival motor neuron protein | |
| Rabbit | |
| Antigen affinity chromatography | |
| RUO | |
| 6606 | |
| 4° C | |
| Liquid |
| Immunoprecipitation | |
| 1 mg/ml | |
| phosphate, tris citrate with 0.09% sodium azide; pH 7-8 | |
| Q16637 | |
| SMN1 | |
| Between 50 and 100 | |
| 10 μL | |
| Primary | |
| Human | |
| Antibody | |
| IgG |
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