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MAB21L1 is similar to the MAB-21 cell fate-determining gene found in C. Additionally we are shipping MAB21L1 Proteins (9) and many more products for this protein.
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Despite the absence of conserved non-coding elements, a 4.9-kb mab21l2 promoter is sufficient to recapitulate expression in tissues unique to mab21l1 or mab21l2.
Data revealed that expression of DNA binding inhibitor 3 (show PPP1R11 Antibodies), early B cell factor 2 (show EBF2 Antibodies), Ebf3 (show EBF3 Antibodies), Iroquois related homeobox 1 (show IRX1 Antibodies), Kruppel-like factor 7 , mab-21-like 1 , fatty acid binding protein 7 (show FABP7 Antibodies) and stathmin-like 4 (show STMN4 Antibodies),were enriched in the diencephalon of zebrafish.
We hypothesize that MAB21L1 haploinsufficiency cause a previously undescribed syndrome with scrotal agenesis, ophthalmological anomalies, facial dysmorphism and gross psychomotor delay as remarkable hallmarks.
MEF is involved in PTH (show PTH Antibodies) suppression of osteoblasts through activating the MKK4 (show MAP2K4 Antibodies)/JNK1 (show MAPK8 Antibodies) pathway and subsequently up-regulating Mab21l1 expression.
This gene is similar to the MAB-21 cell fate-determining gene found in C. elegans. It may be involved in eye and cerebellum development, and it has been proposed that expansion of a trinucleotide repeat region in the 5' UTR may play a role in a variety of psychiatric disorders.
protein mab-21-like 1
, cell fate determination protein
, mab-21-like protein 1