MKS1 Polyclonal Antibody
| 规格： | / 20μL / 60μL / 120μL / 200μL |
| 价格： | / ￥420 / ￥1010 / ￥1640 / ￥2365 |
货号：E-AB-19009
宿主: Rabbit
反应性: H,M,R
应用: WB,IHC
Overview
| Synonyms | B8d3,BBS13,Dysencephalia splanchnocystica,FABB proteome like protein,FLJ20345,Gruber syndrome,Meckel gruber syndrome,Meckel gruber syndrome type 1,Meckel syndrome,Meckel syndrome type 1,Meckel syndrome type 1 protein,Meckel syndrome type 1 protein homolog,MES,MKS 1,MKS,Mks1,MKS1,POC12,POC12 centriolar protein homolog,MKS1抗体 |
| Swissprot | Q9NXB0 |
| Source | Rabbit |
| Reactivity | Human,Mouse,Rat |
| Immunogen | Fusion protein of human MKS1 |
| Application | WB(Detection kit: E-IR-R304),IHC(Detection kit: E-IR-R213) |
| Recommended dilution | WB,,1:500-1:2000;IHC,,1:30-1:150; |
| Concentration | 0.9mg/mL |
| Clonality | Polyclonal |
Properties
| Cellular localization | Cytoplasm>cytoskeleton>cilium basal body. Cytoplasm>cytoskeleton>microtubule organizing center>centrosome. Localizes at the transition zone, a region between the basal body and the ciliary axoneme. |
| 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 localizes to the basal body and is required for formation of the primary cilium in ciliated epithelial cells. Mutations in this gene result in Meckel syndrome type 1 and in Bardet-Biedl syndrome type 13. Multiple transcript variants encoding different isoforms have been found for this gene. |
