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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 416-445, 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)), Enzyme Immunoassay (EIA)
- 特异性
- Recognizes SEPN1 (C-term).
- 纯化方法
- Protein A column followed by peptide Affinity purification
- 免疫原
- KLH conjugated synthetic peptide between 416-445 amino acids from the C-terminal region of Human SEPN1 Genename: SEPN1
- 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 417-445), (C-Term) antibodySEPN1 适用: 人 WB, IHC (p) 宿主: 兔 Polyclonal RB31326 unconjugated
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- 应用备注
- Optimal working dilution should be determined by the investigator.
- 限制
- 仅限研究用
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- 状态
- Liquid
- 浓度
- 0.25 mg/mL
- 缓冲液
- PBS with 0.09 % (W/V) Sodium Azide as preservative
- 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.
- 注意事项
- Avoid repeated freezing and thawing.
- 储存条件
- 4 °C/-20 °C
- 储存方法
- Store the antibody undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
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- 抗原
- SEPN1 (Selenoprotein N, 1 (SEPN1))
- 别名
- Selenoprotein N (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.Synonyms: SELN
- 基因ID
- 57190
- NCBI登录号
- NP_065184
- 途径
- Skeletal Muscle Fiber Development
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