ZFHX4 Polyclonal Antibody
Product Specifications
Background
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.
Gene ID
79776
Swiss Prot
Q86UP3
Cross Reactivity
Human; Mouse
Clonality
Polyclonal
Source
Rabbit
Applications
IHC-p; IF (paraffin section)
Dilution
IHC-p 1:50-300
Buffer
Liquid in PBS containing 50% glycerol, and 0.02% sodium azide.
Molecular Weight
392
Storage Conditions
-20°C/1 year
Protein Weight
392
Available Sizes
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