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- 抗原 See all DPCD 抗体
- DPCD (Deleted in Primary Ciliary Dyskinesia Homolog (DPCD))
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适用
- 人, 小鼠, 大鼠
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宿主
- 兔
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克隆类型
- 多克隆
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标记
- This DPCD antibody is un-conjugated
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应用范围
- ELISA, Immunohistochemistry (IHC)
- 产品特性
- Polyclonal Antibody
- 纯化方法
- Antigen affinity purification
- 免疫原
- Synthetic peptide of human DPCD
- 亚型
- IgG
- Top Product
- Discover our top product DPCD Primary Antibody
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anti-Deleted in Primary Ciliary Dyskinesia Homolog (DPCD) antibody
DPCD 适用: 人 WB, IHC, IF, IHC (p) 宿主: 小鼠 Monoclonal 8A12 unconjugated
anti-Deleted in Primary Ciliary Dyskinesia Homolog (DPCD) (AA 36-85) antibodyDPCD 适用: 人, 小鼠, 大鼠, 兔, 豚鼠, 马, Bat, Hamster, Pig, 猴 WB 宿主: 兔 Polyclonal unconjugated
anti-Deleted in Primary Ciliary Dyskinesia Homolog (DPCD) (AA 72-121) antibodyDPCD 适用: 人, 小鼠, 大鼠, 兔, 豚鼠, 马, 犬, Bat, Hamster, Pig WB 宿主: 兔 Polyclonal unconjugated
anti-Deleted in Primary Ciliary Dyskinesia Homolog (DPCD) (N-Term) antibodyDPCD 适用: 人, 小鼠 WB 宿主: 兔 Polyclonal unconjugated
anti-Deleted in Primary Ciliary Dyskinesia Homolog (DPCD) (AA 96-136) antibodyDPCD 适用: 人, 小鼠 WB 宿主: 兔 Polyclonal RB27182 unconjugated
anti-Deleted in Primary Ciliary Dyskinesia Homolog (DPCD) (Middle Region) antibodyDPCD 适用: 人, 小鼠, 大鼠, 兔, 豚鼠, 马, 犬, Cow WB 宿主: 兔 Polyclonal unconjugated
anti-Deleted in Primary Ciliary Dyskinesia Homolog (DPCD) (N-Term) antibodyDPCD 适用: 人, 小鼠, 大鼠, 兔, 豚鼠, 马, 犬, Cow WB 宿主: 兔 Polyclonal unconjugated
anti-Deleted in Primary Ciliary Dyskinesia Homolog (DPCD) (AA 99-140), (Middle Region) antibodyDPCD 适用: 人, 小鼠 WB, EIA 宿主: 兔 Polyclonal unconjugated
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- 应用备注
- IHC 1:50-1:100, ELISA 1:5000-1:10000
- 限制
- 仅限研究用
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- 状态
- Liquid
- 浓度
- 1.5 mg/mL
- 缓冲液
- PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4
- 储存液
- Sodium azide
- 注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- 储存条件
- -20 °C
- 储存方法
- Store at -20°C. Avoid freeze / thaw cycles.
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- 抗原
- DPCD (Deleted in Primary Ciliary Dyskinesia Homolog (DPCD))
- 别名
- DPCD (DPCD 产品)
- 背景
- This gene in mouse encodes a protein that may be involved in the generation and maintenance of ciliated cells. In mouse, expression of this gene increases during ciliated cell differentiation, and disruption of this gene has been linked to primary ciliary dyskinesia.
- UniProt
- Q9BVM2
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