BBS12 Polyclonal Antibody
| 规格： | / 20μL / 60μL / 120μL / 200μL |
| 价格： | / ￥420 / ￥1010 / ￥1640 / ￥2365 |
货号：E-AB-53593
宿主: Rabbit
反应性: H
应用: IHC
Overview
| Synonyms | Bardet Biedl syndrome 12 protein,Bardet-Biedl syndrome 12 (human),Bardet-Biedl syndrome 12 protein,Bardet-Biedl syndrome 12 protein homolog,BBS12,BBS12 gene,BBS12,C4orf24,FLJ35630,FLJ41559,Gm1805,Gm407,Gm721,RP23-137F6.2,BBS12抗体 |
| Swissprot | Q6ZW61 |
| Source | Rabbit |
| Reactivity | Human |
| Immunogen | Synthetic peptide of human BBS12 |
| Application | IHC(Detection kit: E-IR-R213) |
| Recommended dilution | IHC,,1:40-1:200 |
| Concentration | 0.9mg/mL |
| Clonality | Polyclonal |
Properties
| Cellular localization | Cell projection, cilium. Located within the basal body of the primary cilium of differentiating preadipocytes. |
| Isotype | IgG |
| Purification | Affinity purification |
| Conjugation | Unconjugated |
| Storage instructions | Store at -20℃. Avoid freeze / thaw cycles. |
| Storage buffer | PBS with 0.05% NaN3 and 40% Glycerol,pH7.4 |
| Background | The protein encoded by this gene is part of a complex that is involved in membrane trafficking. The encoded protein is a molecular chaperone that aids in protein folding upon ATP hydrolysis. This protein also plays a role in adipocyte differentiation. Defects in this gene are a cause of Bardet-Biedl syndrome type 12. Two transcript variants encoding the same protein have been found for this gene. |
