FBXW4 anticorps

N° du produit ABIN7264203

Détail du produit anti-FBXW4 anticorps

Antigène: FBXW4 (F-Box and WD Repeat Domain Containing 4 (FBXW4))

Reactivité: Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp FBXW4 est non-conjugé

Application: Western Blotting (WB)

Attributs du produit: Polyclonal Antibody

Purification: Affinity purification

Immunogène: Recombinant fusion protein of human FBXW4 (NP_071322.1).

Isotype: IgG

Information d'application

Indications d'application: WB 1:500-1:2000

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: Store at -20°C. Avoid freeze / thaw cycles.

Détails sur FBXW4

Antigène: FBXW4 (F-Box and WD Repeat Domain Containing 4 (FBXW4))

Autre désignation: FBXW4 (FBXW4 Produits)

Synonymes: anticorps dac, anticorps hag, anticorps hagoromo, anticorps wu:fk63g06, anticorps FBXW4, anticorps DAC, anticorps FBW4, anticorps FBWD4, anticorps SHFM3, anticorps SHSF3, anticorps Dac, anticorps Fbw4, anticorps dactylin, anticorps dactylyn, anticorps F-box and WD repeat domain containing 4, anticorps F-box and WD-40 domain protein 4, anticorps fbxw4, anticorps FBXW4, anticorps Fbxw4

Sujet: 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.

Poids moléculaire:

Observed_MW: 46 kDa

Calculated_MW: 46 kDa

ID gène: 6468

UniProt: P57775