ZFHX4 rabbit pAb

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.

79776

Q86UP3

Nucleus.

Rabbit

Human, Mouse

Synthesized peptide derived from part region of human protein

Polyclonal

WB, IHC, IF

1 year

1 mg/mL

WB: 1:500-1000 IHC: 1:200-500

392kD

PBS with 0.02% sodium azide and 50% glycerol pH 7.4. Store at -20°C. Avoid repeated freeze-thaw cycles.