MYOZ2 抗体 (AA 1-264)
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北京 101111
Quick Overview for MYOZ2 抗体 (AA 1-264) (ABIN6144299)
抗原
See all MYOZ2 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 1-264
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序列
- MLSHNTMMKQ RKQQATAIMK EVHGNDVDGM DLGKKVSIPR DIMLEELSHL SNRGARLFKM RQRRSDKYTF ENFQYQSRAQ INHSIAMQNG KVDGSNLEGG SQQAPLTPPN TPDPRSPPNP DNIAPGYSGP LKEIPPEKFN TTAVPKYYQS PWEQAISNDP ELLEALYPKL FKPEGKAELP DYRSFNRVAT PFGGFEKASR MVKFKVPDFE LLLLTDPRFM SFVNPLSGRR SFNRTPKGWI SENIPIVITT EPTDDTTVPE SEDL
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交叉反应
- 人, 小鼠, 大鼠
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产品特性
- Polyclonal Antibodies
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免疫原
- Recombinant fusion protein containing a sequence corresponding to amino acids 1-264 of human MYOZ2 (NP_057683.1).
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亚型
- IgG
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anti-Myozenin 2 (MYOZ2) (AA 90-180) antibody
MYOZ2 适用: 人 WB, ELISA, IF, IHC 宿主: 兔 Polyclonal unconjugated
anti-Myozenin 2 (MYOZ2) (AA 1-264) antibodyMYOZ2 适用: 人 WB, ELISA 宿主: 小鼠 Monoclonal 1D4 unconjugated
anti-Myozenin 2 (MYOZ2) antibodyMYOZ2 适用: 人 WB, ELISA 宿主: 兔 Polyclonal unconjugated
anti-Myozenin 2 (MYOZ2) antibodyMYOZ2 适用: 人, 小鼠 WB, ELISA 宿主: 兔 Polyclonal unconjugated
anti-Myozenin 2 (MYOZ2) antibodyMYOZ2 适用: 人, 小鼠 ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-Myozenin 2 (MYOZ2) antibodyMYOZ2 适用: 人, 小鼠, 大鼠 IF 宿主: 兔 Polyclonal unconjugated
anti-Myozenin 2 (MYOZ2) (AA 1-264) antibodyMYOZ2 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
anti-Myozenin 2 (MYOZ2) antibodyMYOZ2 适用: 人 WB, IF, IC 宿主: 兔 Polyclonal unconjugated
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应用备注
- WB,1:500 - 1:2000,IF,1:50 - 1:100
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说明
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HIGH QUALITY
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限制
- 仅限研究用
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状态
- Liquid
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缓冲液
- PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.
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储存液
- Sodium azide
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注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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储存条件
- -20 °C
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储存方法
- Store at -20°C. Avoid freeze / thaw cycles.
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- MYOZ2 (Myozenin 2 (MYOZ2))
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别名
- MYOZ2
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背景
- The protein encoded by this gene belongs to a family of sarcomeric proteins that bind to calcineurin, a phosphatase involved in calcium-dependent signal transduction in diverse cell types. These family members tether calcineurin to alpha-actinin at the z-line of the sarcomere of cardiac and skeletal muscle cells, and thus they are important for calcineurin signaling. Mutations in this gene cause cardiomyopathy familial hypertrophic type 16, a hereditary heart disorder.,MYOZ2,C4orf5,CMH16,CS-1,Signal Transduction,Cell Biology & Developmental Biology,Cytoskeleton,Microfilaments,Actins,Cardiovascular,Heart,Contractility,MYOZ2
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分子量
- 29 kDa
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基因ID
- 51778
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UniProt
- Q9NPC6
抗原
-
