Dgcr2, Rabbit, Polyclonal Antibody, Abnova, Rabbit Polyclonal Antibody Raised Against Recombinant Dgcr2, Each

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Deletions of the 22q11.2 Have been associated with a wide range of developmental defects (notably digeorge syndrome, velocardiofacial syndrome, conotruncal anomaly face syndrome and isolated conotruncal cardiac defects) classified under the acronym catch 22. The dgcr2 gene encodes a novel putative adhesion receptor protein, which could play a role in neural crest cells migration, a process which has been proposed to be altered in digeorge syndrome. [Provided by refseqsequence: rfsrkcptgwhhyegtascyrvylsgenywdaaqtcqrlngslatfstdqelrfvlaqewdqpersfgwkdqrklwvgyqyvitgrnrslegrwevafkgssevflppdpifasamsendnvfcaqlqcfhfptlrhhdlhswhaescyekssflckrsqtcvdikdnvvdegfyftpk