This is an aptamer development services to screening aptamers binds to the BSCL2 with an affinity of 1nM~1μM.
To download a Certificate of Analysis, please enter a lot number in the search box below. Note: Certificate of Analysis not available for kit components.
| Target Category | Protein |
| Target | BSCL2 |
| Alternative Names | BSCL2 Lipid Droplet Biogenesis Associated, Seipin; Seipin; Bernardinelli-Seip Congenital Lipodystrophy Type 2 Protein; Berardinelli-Seip Congenital Lipodystrophy 2 (Seipin) ; BSCL2, Seipin Lipid Droplet Biogenesis Associated; Spastic Paraplegia 17 (Silver Syndrome) ; GNG3LG; HMN5C; SPG17; BSCL2; HMN5; PELD |
| Gene ID | 26580 |
| UniProt ID | Q96G97 |
| Target Overview | This gene encodes the multi-pass transmembrane protein protein seipin. This protein localizes to the endoplasmic reticulum and may be important for lipid droplet morphology. Mutations in this gene have been associated with congenital generalized lipodystrophy type 2 or Berardinelli-Seip syndrome, a rare autosomal recessive disease characterized by a near absence of adipose tissue and severe insulin resistance. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. Naturally occurring read-through transcription occurs between this locus and the neighboring locus HNRNPUL2 (heterogeneous nuclear ribonucleoprotein U-like 2). |
| Chemical Modification | N/A |
| Type | DNA |
| Length | 20-80 nt |
| Affinity (Kd) | 1nM~1μM |
| Binding Conditions/Buffer | PBS; buffer system with Serum; other |