FBXW4 抗体 (AA 171-270)
Quick Overview for FBXW4 抗体 (AA 171-270) (ABIN1386820)
抗原
See all FBXW4 抗体适用
宿主
克隆类型
标记
应用范围
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抗原表位
- AA 171-270
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交叉反应
- 大鼠
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预测反应
- Human,Mouse
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纯化方法
- Purified by Protein A.
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免疫原
- KLH conjugated synthetic peptide derived from human SHFM3
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亚型
- IgG
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anti-F-Box and WD Repeat Domain Containing 4 (FBXW4) (AA 143-412) antibody
FBXW4 适用: 人 WB, ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-F-Box and WD Repeat Domain Containing 4 (FBXW4) (AA 341-370), (C-Term) antibodyFBXW4 适用: 人 WB 宿主: 兔 Polyclonal RB42400 unconjugated
anti-F-Box and WD Repeat Domain Containing 4 (FBXW4) (AA 41-140) antibodyFBXW4 适用: 人 WB, ELISA 宿主: 小鼠 Polyclonal unconjugated
anti-F-Box and WD Repeat Domain Containing 4 (FBXW4) (AA 1-412) antibodyFBXW4 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
anti-F-Box and WD Repeat Domain Containing 4 (FBXW4) (AA 334-383) antibodyFBXW4 适用: 人, 小鼠, 大鼠, Cow, 豚鼠, 马, 兔, 犬, 猴, Bat, Pig WB 宿主: 兔 Polyclonal unconjugated
anti-F-Box and WD Repeat Domain Containing 4 (FBXW4) (C-Term) antibodyFBXW4 适用: 人, 小鼠, 大鼠, Cow, 豚鼠, 马, 兔, 犬 WB 宿主: 兔 Polyclonal unconjugated
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应用备注
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ELISA 1:500-1000
IHC-P 1:200-400 -
限制
- 仅限研究用
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状态
- Liquid
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浓度
- 1 μg/μL
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缓冲液
- 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.
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储存液
- ProClin
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注意事项
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
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储存条件
- 4 °C,-20 °C
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储存方法
- Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
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有效期
- 12 months
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- FBXW4 (F-Box and WD Repeat Domain Containing 4 (FBXW4))
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别名
- SHFM3
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背景
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Synonyms: DAC, Dactylin, F box and WD 40 domain containing protein 4, F box and WD 40 domain protein 4, F box and WD repeat domain containing 4, F box/WD repeat containing protein 4, F box/WD repeat protein 4, F-box and WD-40 domain-containing protein 4, F-box/WD repeat-containing protein 4, FBW 4, FBW4, FBWD 4, FBWD4, FBXW 4, FBXW4, FBXW4_HUMAN, SHFM 3, SHSF 3, SHSF3, Split hand/foot malformation ectrodactyly type.
Background: Probably recognizes and binds to some phosphorylated proteins and promotes their ubiquitination and degradation. Likely to be involved in key signaling pathways crucial for normal limb development. May participate in Wnt signaling.Involvement in disease:Defects in FBXW4 are a cause of split-hand/foot malformation type 3 (SHFM3) . SHFM3 is an autosomal dominant disorder characterized by hypoplasia/aplasia of the central digits with fusion of the remaining digits.
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基因ID
- 6468
抗原
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