ZIC2 antibody can be used for detection of ZIC2 by ELISA at 1:62500. ZIC2 antibody can be used for detection of ZIC2 by western blot at 0.25 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.
Beschränkungen
Nur für Forschungszwecke einsetzbar
Format
Lyophilized
Rekonstitution
Add 50 ?L of distilled water. Final antibody concentration is 1 mg/mL.
Konzentration
1 mg/mL
Buffer
Antibody is lyophilized in PBS buffer with 2 % sucrose.
Handhabung
As with any antibody avoid repeat freeze-thaw cycles.
Lagerung
4 °C/-20 °C
Informationen zur Lagerung
For short periods of storage (days) store at 4 °C. For longer periods of storage, store ZIC2 antibody at -20 °C.
HPE5 antikoerper, Ku antikoerper, cb851 antikoerper, fb26a03 antikoerper, wu:fb26a03 antikoerper, zic2 antikoerper, zic2.1 antikoerper, hpe5 antikoerper, hm:zeh0655 antikoerper, id:ibd5017 antikoerper, zic2.2 antikoerper, zic2l antikoerper, Zic family member 2 antikoerper, zinc finger protein of the cerebellum 2 antikoerper, zic family member 2 (odd-paired homolog, Drosophila), a antikoerper, Zic family member 2 L homeolog antikoerper, zic family member 2 (odd-paired homolog, Drosophila) b antikoerper, ZIC2 antikoerper, Zic2 antikoerper, zic2a antikoerper, zic2.L antikoerper, zic2b antikoerper
Hintergrund
ZIC2 is a member of the ZIC family of C2H2-type zinc finger proteins. This protein functions as a transcriptional repressor and may regulate tissue specific expression of dopamine receptor D1. Mutations in this gene cause holoprosencephaly type 5. Holoprosencephaly is the most common structural anomaly of the human brain. A polyhistidine tract polymorphism in this gene may be associated with increased risk of neural tube defects.This gene encodes a member of the ZIC family of C2H2-type zinc finger proteins. This protein functions as a transcriptional repressor and may regulate tissue specific expression of dopamine receptor D1. Mutations in this gene cause holoprosencephaly type 5. Holoprosencephaly is the most common structural anomaly of the human brain. A polyhistidine tract polymorphism in this gene may be associated with increased risk of neural tube defects. This gene is closely linked to a gene encoding zinc finger protein of the cerebellum 5, a related family member on chromosome 13.