KLHL21 Monoclonal Antibody, 100ul Plasma Defects in this gene are

Defects in this gene are also associated with early onset hypertension with severe exacerbation in pregnancy

NGL1 is a specific binding partner for netrin G1 (NTNG1

Two subgroups of the CEA family

a transcription factor which is activated by androgen and has a key role in male sexual differentiation

antiapoptotic

KLHL21 Monoclonal Antibody, 100ul Plasma Defects in this gene areProbable substrate specific adapter of an E3 ubiquitin protein ligase complex which mediates the ubiquitination and subsequent proteasomal degradation of target proteins.,pathway: Protein modification protein ubiquitination.,similarity: Contains 1 BACK (BTB Kelch associated) domain.,similarity: Contains 1 BTB (POZ) domain.,similarity: Contains 6 Kelch repeats.,subunit: Interacts with cul3.,