ZFHX4 rabbit pAb
Ref. EK-ES10485
50µl | 188.00 € | ||
100µl | 316.00 € |
Product Information
disease:A chromosomal aberration involving [ZFHX4] is found in one patient with ptosis. Translocation t(1;8)(p34.3;q21.12).,function:May play a role in neural and muscle differentiation (By similarity). May be involved in transcriptional regulation.,similarity:Belongs to the krueppel C2H2-type zinc-finger protein family.,similarity:Contains 20 C2H2-type zinc fingers.,similarity:Contains 4 homeobox DNA-binding domains.,tissue specificity:Expressed in brain, skeletal muscle and liver. Very low expression in stomach.,
Chemical properties
Technical inquiry about: EK-ES10485 ZFHX4 rabbit pAb
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