PLC Beta2 Polyclonal Antibody, 50ul Drug Development and Evaluation Defects in this gene are

Defects in this gene are the cause of deutanopic colorblindness

Each 10 mL bottle contains 50 Units/μL activity for efficient cap-methylation

and ovalbumin(ov)-serpin subfamily

Loss of function compound heterozygous mutations in this gene were found in a human patient affected by the Walker-Warburg syndrome (WWS) phenotype

which is activated by binding of small GTPases such as CDC42 to an N-terminal regulatory domain

PLC Beta2 Polyclonal Antibody, 50ul Drug Development and Evaluation Defects in this gene arePLCB2 (Phospholipase C Beta 2) is a Protein Coding gene. Diseases associated with PLCB2 include prostate leiomyosarcoma. Among its related pathways are cGMP PKG signaling pathway and African trypanosomiasis. GO annotations related to this gene include calcium ion binding and phosphoric diester hydrolase activity. An important paralog of this gene is PLCB3.