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SHFM3 Rabbit anti-Human, Polyclonal, Bioss
SDP

Catalog No. 501988522
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100 μL
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50-198-8522 100 μL
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Catalog No. 50-198-8522 Supplier Bioss Supplier No. BS8390R
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Rabbit Polyclonal Antibody

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.

Specifications

Antigen SHFM3
Applications Immunofluorescence, Immunohistochemistry (Paraffin)
Classification Polyclonal
Concentration 1 μg/mL
Conjugate Unconjugated
Formulation PBS with 1% BSA, 50% glycerol and 0.09% sodium azide; pH
Gene FBXW4
Gene Accession No. P57775
Gene Alias BOS_23470; DAC; dactylaplasia; Dactylin; dactylyn; 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 protein Fbw4; F-box/WD repeat protein 4; F-box/WD repeat-containing protein 4; FBW4; FBWD4; FBXW4; Protein hagoromo; SHFM3; SHSF3
Gene Symbols FBXW4
Host Species Rabbit
Immunogen KLH conjugated synthetic peptide derived from human SHFM3.
Purification Method Protein A
Quantity 100 μL
Regulatory Status RUO
Primary or Secondary Primary
Gene ID (Entrez) 6468
Target Species Human
Content And Storage -20°C
Product Type Antibody
Form Liquid
Isotype IgG
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