Dysferlin 抗体
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北京 101111
Quick Overview for Dysferlin 抗体 (ABIN7266868)
抗原
See all Dysferlin (DYSF) 抗体适用
宿主
克隆类型
标记
应用范围
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原理
- Dysferlin (Romeo) Rabbit mAb
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交叉反应
- 人, 小鼠
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产品特性
- Monoclonal Antibodies
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纯化方法
- Affinity purification
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免疫原
- A synthesized peptide derived from human Dysferlin (Romeo)
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亚型
- IgG
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anti-Dysferlin (DYSF) (AA 105-278) antibody
DYSF 适用: 人 ELISA, IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-Dysferlin (DYSF) (C-Term) antibodyDYSF 适用: 人, 小鼠, 大鼠 WB, ELISA, IHC, IF, ICC 宿主: 兔 Polyclonal unconjugated
anti-Dysferlin (DYSF) antibodyDYSF 适用: 人 WB, ELISA 宿主: 兔 Polyclonal unconjugated
anti-Dysferlin (DYSF) (AA 1584-1633) antibodyDYSF 适用: 人, 小鼠, 豚鼠, 兔, 猴 WB 宿主: 兔 Polyclonal unconjugated
anti-Dysferlin (DYSF) (AA 215-264) antibodyDYSF 适用: 人, Cow, 犬, 豚鼠, 兔, Pig, 猴 WB 宿主: 兔 Polyclonal unconjugated
anti-Dysferlin (DYSF) (AA 1999-2016) antibodyDYSF 适用: 人 IHC, IHC (p), IHC (fro) 宿主: 小鼠 Monoclonal Ham1-7B6 unconjugated
anti-Dysferlin (DYSF) (AA 1-479) antibodyDYSF 适用: 人 WB, IHC, ICC, IP 宿主: 兔 Polyclonal unconjugated
anti-Dysferlin (DYSF) (C-Term) antibodyDYSF 适用: 人, 小鼠, 大鼠, Cow, 犬, Pig WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-Dysferlin (DYSF) (Middle Region) antibodyDYSF 适用: 人, 小鼠, 大鼠, Cow, 犬, 豚鼠, 兔, 马, 斑马鱼 WB 宿主: 兔 Polyclonal unconjugated
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应用备注
- WB,1:500 - 1:2000,IHC,1:50 - 1:200
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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,0.05 % BSA,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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- Dysferlin (DYSF)
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别名
- DYSF
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背景
- The protein encoded by this gene belongs to the ferlin family and is a skeletal muscle protein found associated with the sarcolemma. It is involved in muscle contraction and contains C2 domains that play a role in calcium-mediated membrane fusion events, suggesting that it may be involved in membrane regeneration and repair. In addition, the protein encoded by this gene binds caveolin-3, a skeletal muscle membrane protein which is important in the formation of caveolae. Specific mutations in this gene have been shown to cause autosomal recessive limb girdle muscular dystrophy type 2B (LGMD2B) as well as Miyoshi myopathy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2008],FER1L1, LGMD2B, MMD1,Cell Biology & Developmental Biology,DYSF
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分子量
- 280kDa
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基因ID
- 8291
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UniProt
- O75923
抗原
-
