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F166B Rabbit Polyclonal Antibody, 50ul Shakers The molecular defects in complementation

SKU: 45074653283

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F166B Rabbit Polyclonal Antibody, 50ul Shakers The molecular defects in complementation

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Description

The molecular defects in complementation groups B| C| and D all lead to a deficiency in RFX| a nuclear protein complex that binds to the X box of MHC-II promoters

The encoded protein can depolymerize microtubules at the plus end

This gene encodes a member of the inward rectifier-type potassium channel family

Probably inactive as a glycosidase

Transient role during the earliest stages of myocardial cell differentiation and/or primitive chamber formation and may also be important for the earliest stages of skeletal muscle growth and/or differentiation

F166B Rabbit Polyclonal Antibody, 50ul Shakers The molecular defects in complementation

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