ab171870 - Rabbit polyclonal IgG, is suitable for use as an isotype control with this antibody.
1/10 - 1/50. Perform heat mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol.
Expression appears to be maximal in germinal vesicle oocytes, it tails off through metaphase II oocytes and is undetectable following the completion of the oocyte to embryo transition.
Involvement in disease
Defects in KHDC3L are the cause of hydatidiform mole recurrent type 2 (HYDM2) [MIM:614293]. A disorder characterized by excessive trophoblast development that produces a growing mass of tissue inside the uterus at the beginning of a pregnancy. It leads to abnormal pregnancies with no embryo, and cystic degeneration of the chorionic villi.
Belongs to the KHDC1 family. Contains 1 KH domain.
Contains an atypical KH domain with amino acid changes at critical sites, suggesting that it may not bind RNA.