ZFHX4 rabbit pAb

• 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.

• Description :

  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.

• UniProt :

  Q86UP3

• Swiss Prot :

  Q86UP3

• Reactivity :

  Human; Mouse

• Immunogen :

  Synthesized peptide derived from part region of human protein

• Target :

  ZFHX4

• Clonality :

  Polyclonal

• Source :

  Rabbit

• Applications :

  WB; IHC; IF

• Concentration :

  1 mg/ml

• Dilution :

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

• Buffer :

  -20°C/1 year

• Molecular Weight :

  392kD

• Storage Conditions :

  -20°C/1 year

• Observed Molecular Weight :

  392kD

• Fragment :

  IgG

• Subcellular Location :

  Nucleus .

• Gene ID (Human) :

  79776