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- 抗原 See all TMEM67 抗体
- TMEM67 (Transmembrane Protein 67 (TMEM67))
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抗原表位
- AA 780-940
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适用
- 人
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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 TMEM67 antibody is un-conjugated
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应用范围
- Western Blotting (WB)
- 原理
- TMEM67 Rabbit pAb
- 序列
- LSHKCFGYYI HGRSVHGHAD TNMEEMNMNL KREAENLCSQ RGLVPNTDGQ TFEIAISNQM RQHYDRIHET LIRKNGPARL LSSSASTFEQ SIKAYHMMNK FLGSFIDHVH KEMDYFIKDK LLLERILGME FMEPMEKSIF YNDEGYSFSS VLYYGNEATL L
- 交叉反应
- 小鼠, 大鼠
- 产品特性
- Polyclonal Antibodies
- 纯化方法
- Affinity purification
- 免疫原
- Recombinant fusion protein containing a sequence corresponding to amino acids 780-940 of human TMEM67 (NP_714915.3).
- 亚型
- IgG
- Top Product
- Discover our top product TMEM67 Primary Antibody
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anti-Transmembrane Protein 67 (TMEM67) (AA 241-500) antibody
TMEM67 适用: 人 ELISA, IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-Transmembrane Protein 67 (TMEM67) (Internal Region) antibodyTMEM67 适用: 人, 小鼠 WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-Transmembrane Protein 67 (TMEM67) (C-Term) antibodyTMEM67 适用: 人 ELISA, WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-Transmembrane Protein 67 (TMEM67) (Center) antibodyTMEM67 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-Transmembrane Protein 67 (TMEM67) antibodyTMEM67 适用: 小鼠, 大鼠 WB 宿主: 兔 Polyclonal unconjugated
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- 应用备注
- WB,1:200 - 1:2000
- 限制
- 仅限研究用
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- 状态
- Liquid
- 缓冲液
- PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.
- 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
- TMEM67 (Transmembrane Protein 67 (TMEM67))
- 别名
- TMEM67 (TMEM67 产品)
- 别名
- JBTS6 antibody, MECKELIN antibody, MKS3 antibody, NPHP11 antibody, TNEM67 antibody, 5330408M12Rik antibody, B230117O07 antibody, b2b1163.1Clo antibody, b2b1291.1Clo antibody, Wpk antibody, transmembrane protein 67 antibody, TMEM67 antibody, tmem67 antibody, Tmem67 antibody
- 背景
- The protein encoded by this gene localizes to the primary cilium and to the plasma membrane. The gene functions in centriole migration to the apical membrane and formation of the primary cilium. Multiple transcript variants encoding different isoforms have been found for this gene. Defects in this gene are a cause of Meckel syndrome type 3 (MKS3) and Joubert syndrome type 6 (JBTS6).,TMEM67,JBTS6,MECKELIN,MKS3,NPHP11,TNEM67,meckelin,TMEM67
- 分子量
- 103kDa/111kDa
- 基因ID
- 91147
- UniProt
- Q5HYA8
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