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Angiotensinogen (serpin Peptidase Inhibitor, Clade A, Member 8) (AGT) Peptide

AGT 适用: 哺乳动物 宿主: 合成 WB, BP, IHC
产品编号 ABIN939371
发货至: 中国
  • 抗原 See all AGT products
    AGT (Angiotensinogen (serpin Peptidase Inhibitor, Clade A, Member 8) (AGT))
    蛋白类型
    Synthetic
    宿主
    哺乳动物
    资源
    • 4
    合成
    应用范围
    Western Blotting (WB), Blocking Peptide (BP), Immunohistochemistry (IHC)
    序列
    IHPFHLVIHN ESTCEQLAKA NAGKPKDPTF IPAPIQAKTS PVDEKALQDQ
    产品特性
    A synthetic peptide for use as a blocking control in assays to test for specificity of AGT antibody,
    Alternative Names: AGT control peptide, AGT antibody Blocking Peptide, Anti-AGT Blocking Peptide, Angiotensinogen Blocking Peptide, Serpin Peptidase Inhibitor Clade A 8 Blocking Peptide, ANHU Blocking Peptide, SERPINA8 Blocking Peptide
  • 应用备注
    Optimal conditions should be determined by the investigator
    限制
    仅限研究用
  • 状态
    Lyophilized
    溶解方式
    Add 100 µL of distilled water for a final peptide concentration is 1 mg/mL.
    缓冲液
    PBS
    注意事项
    Avoid repeated freeze/thaw cycles.
    储存条件
    -20 °C
    储存方法
    Store at -20 °C long term.
  • 抗原
    AGT (Angiotensinogen (serpin Peptidase Inhibitor, Clade A, Member 8) (AGT))
    别名
    ANHU Peptide, SERPINA8 Peptide, AI265500 Peptide, AngI Peptide, AngII Peptide, Aogen Peptide, Serpina8 Peptide, ANRT Peptide, Ang Peptide, PAT Peptide, wu:fb62f06 Peptide, wu:fj87b02 Peptide, zgc:111892 Peptide, AGT Peptide, angt Peptide, ANGT Peptide, angiotensinogen Peptide, angiotensinogen (serpin peptidase inhibitor, clade A, member 8) Peptide, AGT Peptide, Agt Peptide, agt Peptide
    背景
    AGT, pre-angiotensinogen or angiotensinogen precursor, is expressed in the liver and is cleaved by the enzyme renin in response to lowered blood pressure. The resulting product, angiotensin I, is then cleaved by angiotensin converting enzyme (ACE) to generate the physiologically active enzyme angiotensin II. The protein is involved in maintaining blood pressure and in the pathogenesis of essential hypertension and preeclampsia. Mutations in this gene are associated with susceptibility to essential hypertension, and can cause renal tubular dysgenesis, a severe disorder of renal tubular development. Defects in this gene have also been associated with non-familial structural atrial fibrillation, and inflammatory bowel disease.
    分子量
    53 kDa
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