ZNF703 Polyclonal Antibody
| 规格： | / 20μL / 60μL / 120μL / 200μL |
| 价格： | / ￥420 / ￥1010 / ￥1640 / ￥2365 |
货号：E-AB-19556
宿主: Rabbit
反应性: H,M
应用: IHC
Overview
| Synonyms | FLJ14299,ZEPPO1,Zinc finger elbow-related proline domain protein 1,Zinc finger protein 703,ZN703,ZNF503L,znf703,ZPO1,ZNF703抗体 |
| Swissprot | Q9H7S9 |
| Source | Rabbit |
| Reactivity | Human, Mouse |
| Immunogen | Synthetic peptide of human ZNF703 |
| Application | IHC(Detection kit: E-IR-R213) |
| Recommended dilution | IHC,,1:30-1:150 |
| Concentration | 1.2mg/mL |
| Clonality | Polyclonal |
Properties
| Cellular localization | Nucleus. |
| 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 | ZNF703 (zinc finger protein 703) is a 590 amino acid nuclear protein that contains one C2H2-type zinc finger and is thought to play a role in transcriptional regulation. Multiple isoforms of ZNF703 exist due to alternative splicing events. The gene encoding ZNF703 maps to human chromosome 8, which consists of nearly 146 million base pairs, houses more than 800 genes and is associated with a variety of diseases and malignancies. Schizophrenia, bipolar disorder, Trisomy 8, Pfeiffer syndrome, congenital hypothyroidism, Waardenburg syndrome and some leukemias and lymphomas are thought to occur as a result of defects in specific genes that map to chromosome 8. |
