FBXW4 anticorps (C-Term)
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- Antigène Voir toutes FBXW4 Anticorps
- FBXW4 (F-Box and WD Repeat Domain Containing 4 (FBXW4))
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Épitope
- AA 341-370, C-Term
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Reactivité
- Humain
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp FBXW4 est non-conjugé
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Application
- Western Blotting (WB)
- Purification
- This antibody is purified through a protein A column, followed by peptide affinity purification.
- Immunogène
- This FBXW4 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 341-370 amino acids from the C-terminal region of human FBXW4.
- Isotype
- Ig Fraction
- Top Product
- Discover our top product FBXW4 Anticorps primaire
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- Indications d'application
- For WB starting dilution is: 1:1000
- Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 0.42 mg/mL
- Buffer
- Supplied in PBS with 0.09 % (W/V) sodium azide.
- 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
- 4 °C,-20 °C
- Stockage commentaire
- Store at 4°C for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.
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- 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
- 46 kDa
- ID gène
- 6468
- UniProt
- P57775
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