ZFHX4 rabbit pAb

Sizes: 50μL, 100μL

Catalogue Numbers: ES10485-50, ES10485-100

Citations, Manuals and MSDS Available upon request.

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.,

Source: Rabbit

Applications: WB; IHC; IF

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

Reactivity: Human; Mouse

Immunogen: Synthesized peptide derived from part region of human protein

Storage and Stability: -20°C/1 year

Clonality: Polyclonal

Isotype: IgG

Concentration: 1 mg/ml

Observed Band (KD): 392kD

Human Gene ID: 79776

Human SWISS Prot NO: Q86UP3

Subcellular Location: Nucleus

Research Use Only