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The protein encoded by KHDC3L belongs to the KHDC1 family, members of which contain an atypical KH domain that may not bind RNA like canonical KH domains. Additionally we are shipping and many more products for this protein.
Showing 10 out of 34 products:
Human Polyclonal KHDC3L Primary Antibody for FACS, IHC (p) - ABIN655185
Pierre, Gautier, Callebaut, Bontoux, Jeanpierre, Pontarotti, Monget: Atypical structure and phylogenomic evolution of the new eutherian oocyte- and embryo-expressed KHDC1/DPPA5/ECAT1/OOEP gene family. in Genomics 2007
Show all 4 references for ABIN655185
Human Polyclonal KHDC3L Primary Antibody for EIA, FACS - ABIN952017
Mitsui, Tokuzawa, Itoh, Segawa, Murakami, Takahashi, Maruyama, Maeda, Yamanaka: The homeoprotein Nanog is required for maintenance of pluripotency in mouse epiblast and ES cells. in Cell 2003
Show all 2 references for ABIN952017
No disease-causing mutations were identified in NLRP2 (show NLRP2 Antibodies), NLRP7 (show NLRP7 Antibodies) and KHDC3L in cohorts of unexplained infertility and recurrent pregnancy loss.
NLRP7 (show NLRP7 Antibodies) and KHDC3L localize to the cytoskeleton and are predominant at the cortical region in growing oocytes.
The absence of mutations in women with Androgenetic complete hydatidiform moles supports a role for NLRP7 (show NLRP7 Antibodies) or KHDC3L in Biparental hydatidiform moles only.
Investigation of the association between molar pregnancy and recurrent miscarriages regarding changes in the NLRP7 (show NLRP7 Antibodies) and C6orf221/KHDC3L genes.
Similarities between two recurrent hydatidiform moles (RHM) causative genes, KHDC3L and NLRP7 (show NLRP7 Antibodies), in their subcellular localization, parental contribution to the HM tissues caused by them, and the presence of several founder mutations.
these findings suggest that neither mutations nor variants in NLRP7 (show NLRP7 Antibodies) and C6orf221 are major factors contributing to the risk of these types of pregnancy complications.
Data indicate there was no KHDC3L mutation found in recurrent and sporadic hydatidiform moles Chinese patients.
Both NLRP7 (show NLRP7 Antibodies) and KHDC3L are involved in setting or maintaining the appropriate imprint within the ovum in women with familial recurrent hydatidiform mole.
Observations suggest that although NLRP7 (show NLRP7 Antibodies) and C6orf221 mutations are related to diploid biparental FRHMs, neither of these genes, nor NLRP2 (show NLRP2 Antibodies), are related to diploid HMs (show CTSC Antibodies) with biparental contributions to the molar genome.
Mutations causing familial biparental hydatidiform mole implicate c6orf221 as a possible regulator of genomic imprinting in the human oocyte.
The protein encoded by this gene belongs to the KHDC1 family, members of which contain an atypical KH domain that may not bind RNA like canonical KH domains. This gene is specifically expressed in the oocytes, and recent studies suggest that it may function as a regulator of genomic imprinting in the oocyte. Mutations in this gene are associated with recurrent biparental complete hydatidiform mole.
ES cell-associated transcript 1 protein
, KHDC3-like protein
, ES cell associated transcript 1
, KH domain-containing protein 3
, protein Filia