SHFM3 Overexpression Lysate (Denatured)


FBXW4 transfected lysate.
Lane 1: FBXW4 transfected lysate (45.43 KDa) Lane 2: Non-transfected lysate.

Product Details

Reactivity HuSpecies Glossary
Applications WB
The exact concentration of the protein of interest cannot be determined for overexpression lysates. Please contact technical support for more information.

Order Details

SHFM3 Overexpression Lysate (Denatured) Summary

F-box and WD repeat domain containing 4

Packaging, Storage & Formulations

Store at -80C. Avoid freeze-thaw cycles.
50mM Tris-HCl, 2%SDS, 10% glycerol, 2% 2-mercaptoethanol, pH 6.8.


  • Western Blot
Application Notes
This transient overexpression cell lysate is useful for western blot and was tested with Anti-FBXW4 antibody H00006468-B01 by Western Blots.

Lysate Details for SHFM3

Protein State

Reactivity Notes



This product is produced by and distributed for Abnova, a company based in Taiwan.

Alternate Names for SHFM3 Overexpression Lysate (Denatured)

  • DAC
  • Dactylin
  • F-box and WD repeat domain containing 4
  • F-box and WD-40 domain protein 4
  • F-box and WD-40 domain-containing protein 4
  • F-box/WD repeat protein 4
  • F-box/WD repeat-containing protein 4
  • Fbw4
  • FBW4split hand/foot malformation (ectrodactyly) type 3
  • FBWD4
  • SHFM3
  • SHSF3


This gene is a member of the F-box/WD-40 gene family, which recruit specific target proteins through their WD-40 protein-protein binding domains for ubiquitin mediated degradation. In mouse, a highly similar protein is thought to be responsible for maintaining the apical ectodermal ridge of developing limb buds; disruption of the mouse gene results in the absence of central digits, underdeveloped or absent metacarpal/metatarsal bones and syndactyly. This phenotype is remarkably similar to split hand-split foot malformation in humans, a clinically heterogeneous condition with a variety of modes of transmission. An autosomal recessive form has been mapped to the chromosomal region where this gene is located, and complex rearrangements involving duplications of this gene and others have been associated with the condition. A pseudogene of this locus has been mapped to one of the introns of the BCR gene on chromosome 22. [provided by RefSeq]


This product is for research use only and is not approved for use in humans or in clinical diagnosis. Lysates are guaranteed for 6 months from date of receipt.

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Video Protocols

WB Video Protocol

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Contact Information

Product PDFs


Gene Symbol FBXW4

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