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BARH2 Polyclonal Antibody, 20ul sgRNA customized design disease:Defects in SRY are a
BARH2 Polyclonal Antibody, 20ul sgRNA customized design disease:Defects in SRY are a
BARH2 Polyclonal Antibody, 20ul sgRNA customized design disease:Defects in SRY are a
BARH2 Polyclonal Antibody, 20ul sgRNA customized design disease:Defects in SRY are a

BARH2 Polyclonal Antibody, 20ul sgRNA customized design disease:Defects in SRY are a

SKU: 21076538699

4.2
USD97.20 USD139.20

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BARH2 Polyclonal Antibody, 20ul sgRNA customized design disease:Defects in SRY are aPotential regulator of neural basic helix loop helix genes.,Belongs to the BAR homeobox family.,Contains 1 homeobox DNA binding domain.,

Store: juliusking.com · Domain: juliusking.com

Description

disease:Defects in SRY are a cause of gonadal dysgenesis XY female type (GDXY)

as well as to the cell membrane

A translocation involving FOXO4 on chromosome X and the homolog of the Drosophila trithorax gene

This gene encodes a protein that is required for Notch pathway signaling| and for the activity and accumulation of gamma-secretase

Members of the A/B subfamily of carboxypeptidases

BARH2 Polyclonal Antibody, 20ul sgRNA customized design disease:Defects in SRY are aPotential regulator of neural basic helix loop helix genes.,Belongs to the BAR homeobox family.,Contains 1 homeobox DNA binding domain.,

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