GDF5 抗体 (AbBy Fluor® 750)
Quick Overview for GDF5 抗体 (AbBy Fluor® 750) (ABIN4999838)
抗原
See all GDF5 抗体适用
宿主
克隆类型
标记
应用范围
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交叉反应
- 人, 小鼠
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预测反应
- Rat,Dog,Cow,Pig,Horse,Rabbit
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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 CDMP1/GDF5
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亚型
- IgG
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anti-Growth Differentiation Factor 5 (GDF5) (AA 358-495) antibody
GDF5 适用: 小鼠 WB, IHC, IP, ICC 宿主: 兔 Polyclonal unconjugated
anti-Growth Differentiation Factor 5 (GDF5) (AA 202-501) antibodyGDF5 适用: 人 WB, IHC, ELISA, IF 宿主: 兔 Polyclonal unconjugated
anti-Growth Differentiation Factor 5 (GDF5) (AA 382-501) antibodyGDF5 适用: 人 WB, IHC, IP, ICC 宿主: 兔 Polyclonal unconjugated
anti-Growth Differentiation Factor 5 (GDF5) (Internal Region) antibodyGDF5 适用: 人, 小鼠, 大鼠 WB, ELISA, IHC (p) 宿主: 兔 Polyclonal unconjugated
anti-Growth Differentiation Factor 5 (GDF5) (AA 28-127) antibodyGDF5 适用: 人 WB, ELISA 宿主: 小鼠 Monoclonal 1F4 unconjugated
anti-Growth Differentiation Factor 5 (GDF5) (AA 86-501) antibodyGDF5 适用: 人 WB, IHC, IP, ICC 宿主: 兔 Polyclonal unconjugated
anti-Growth Differentiation Factor 5 (GDF5) antibodyGDF5 适用: 人, 小鼠, 大鼠 WB, IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-Growth Differentiation Factor 5 (GDF5) (AA 376-495) antibodyGDF5 适用: 小鼠 IHC, ELISA 宿主: 兔 Polyclonal unconjugated
anti-Growth Differentiation Factor 5 (GDF5) (AA 13-41), (N-Term) antibodyGDF5 适用: 人 WB, IHC (p) 宿主: 兔 Polyclonal RB01877 unconjugated
anti-Growth Differentiation Factor 5 (GDF5) (AA 350-450) antibodyGDF5 适用: 人 WB, IHC 宿主: 兔 Polyclonal unconjugated
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应用备注
- IF(IHC-P) 1:50-200
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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
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
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储存条件
- -20 °C
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储存方法
- Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
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有效期
- 12 months
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- GDF5 (Growth Differentiation Factor 5 (GDF5))
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别名
- CDMP1
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背景
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Synonyms: Cartilage derived morphogenetic protein 1, Cartilage-derived morphogenetic protein 1, CDMP-1, CDMP1, GDF-5, Gdf 5, GDF5_HUMAN, Growth dferentiation factor 5, Growth/dferentiation factor 5, LAP4, Radotermin.
Background: Defects in GDF5 are the cause of acromesomelic chondrodysplasia Grebe type (AMDG) . Acromesomelic chondrodysplasias are rare hereditary skeletal disorders characterized by short stature, very short limbs, and hand/foot malformations. The severity of limb abnormalities increases from proximal to distal with profoundly affected hands and feet showing brachydactyly and/or rudimentary fingers (knob-like fingers). AMDG is an autosomal recessive form characterized by normal axial skeletons and missing or fused skeletal elements within the hands and feet.Defects in GDF5 are the cause of acromesomelic chondrodysplasia Hunter-Thompson type (AMDH). AMDH is an autosomal recessive form of dwarfism. Patients have limb abnormalities, with the middle and distal segments being most affected and the lower limbs more affected than the upper. AMDH is characterized by normal axial skeletons and missing or fused skeletal elements within the hands and feet.Defects in GDF5 are the cause of brachydactyly type C (BDC). BDC is an autosomal dominant disorder characterized by an abnormal shortness of the fingers and toes.
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基因ID
- 8200
抗原
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