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- 抗原 See all SEPN1 抗体
- SEPN1 (Selenoprotein N, 1 (SEPN1))
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抗原表位
- AA 417-445, C-Term
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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 SEPN1 antibody is un-conjugated
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应用范围
- Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- 纯化方法
- This antibody is purified through a protein A column, followed by peptide affinity purification.
- 免疫原
- This SEPN1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 417-445 amino acids from the C-terminal region of human SEPN1.
- 克隆位点
- RB31326
- 亚型
- Ig Fraction
- Top Product
- Discover our top product SEPN1 Primary Antibody
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anti-Selenoprotein N, 1 (SEPN1) (C-Term) antibody
SEPN1 适用: 人, Cow, 豚鼠, 马, 大鼠, Pig, 斑马鱼, 猴, 犬 WB, IHC, IHC (p) 宿主: 兔 Polyclonal unconjugated
anti-Selenoprotein N, 1 (SEPN1) (C-Term) antibodySEPN1 适用: 人, 小鼠, Cow, Pig, 斑马鱼 WB 宿主: 兔 Polyclonal unconjugated
anti-Selenoprotein N, 1 (SEPN1) (C-Term) antibodySEPN1 适用: 人, 小鼠, Cow, 豚鼠, 马, 大鼠, 斑马鱼 WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-Selenoprotein N, 1 (SEPN1) (C-Term) antibodySEPN1 适用: 人, Cow, 豚鼠, 马, 猴, Bat WB 宿主: 兔 Polyclonal unconjugated
anti-Selenoprotein N, 1 (SEPN1) (AA 416-445), (C-Term) antibodySEPN1 适用: 人 WB, IHC (p), EIA 宿主: 兔 Polyclonal unconjugated
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- 应用备注
- WB: 1:1000. IHC-P: 1:10~50
- 限制
- 仅限研究用
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- 状态
- Liquid
- 缓冲液
- Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.
- 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
- 4 °C,-20 °C
- 储存方法
- SEPN1 Antibody (C-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, place the at -20 °C.
- 有效期
- 6 months
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- 抗原
- SEPN1 (Selenoprotein N, 1 (SEPN1))
- 别名
- SEPN1 (SEPN1 产品)
- 背景
- This gene encodes a selenoprotein, which contains a selenocysteine (Sec) residue at its active site. The selenocysteine is encoded by the UGA codon that normally signals translation termination. The 3' UTR of selenoprotein genes have a common stem-loop structure, the sec insertion sequence (SECIS), that is necessary for the recognition of UGA as a Sec codon rather than as a stop signal. Mutations in this gene cause the classical phenotype of multiminicore disease and congenital muscular dystrophy with spinal rigidity and restrictive respiratory syndrome. Two alternatively spliced transcript variants encoding distinct isoforms have been found for this gene.
- 分子量
- 65813
- 基因ID
- 57190
- NCBI登录号
- NP_065184, NP_996809
- UniProt
- Q9NZV5
- 途径
- Skeletal Muscle Fiber Development
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