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- 抗原 See all ATP7A 抗体
- ATP7A (ATPase, Cu++ Transporting, alpha Polypeptide (ATP7A))
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适用
- 人, 犬
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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 ATP7A antibody is un-conjugated
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应用范围
- Western Blotting (WB)
- 纯化方法
- Purified
- 免疫原
- ATP7 A antibody was raised using a synthetic peptide corresponding to a region with amino acids MKKQIEAMGFPAFVKKQPKYLKLGAIDVERLKNTPVKSSEGSQQRSPSYQ
- Top Product
- Discover our top product ATP7A Primary Antibody
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anti-ATPase, Cu++ Transporting, alpha Polypeptide (ATP7A) (AA 42-61) antibody (HRP)
ATP7A 适用: 人 WB, IHC, IP, IF, ICC 宿主: 小鼠 Monoclonal S60-4 HRP
anti-ATPase, Cu++ Transporting, alpha Polypeptide (ATP7A) (AA 42-61) antibody (FITC)ATP7A 适用: 人 WB, IHC, IP, IF, ICC 宿主: 小鼠 Monoclonal S60-4 FITC
anti-ATPase, Cu++ Transporting, alpha Polypeptide (ATP7A) (AA 42-61) antibody (Biotin)ATP7A 适用: 人 WB, IHC, IP, IF, ICC 宿主: 小鼠 Monoclonal S60-4 Biotin
anti-ATPase, Cu++ Transporting, alpha Polypeptide (ATP7A) (AA 42-61) antibody (PE)ATP7A 适用: 人 WB, IHC, IP, IF, ICC 宿主: 小鼠 Monoclonal S60-4 PE
anti-ATPase, Cu++ Transporting, alpha Polypeptide (ATP7A) (AA 42-61) antibody (APC)ATP7A 适用: 人 WB, IHC, IP, IF, ICC 宿主: 小鼠 Monoclonal S60-4 APC
anti-ATPase, Cu++ Transporting, alpha Polypeptide (ATP7A) (AA 42-61) antibody (PerCP)ATP7A 适用: 人 WB, IHC, IP, IF, ICC 宿主: 小鼠 Monoclonal S60-4 PerCP
anti-ATPase, Cu++ Transporting, alpha Polypeptide (ATP7A) (AA 42-61) antibody (Atto 488)ATP7A 适用: 人 WB, IHC, IP, IF, ICC 宿主: 小鼠 Monoclonal S60-4 Atto 488
anti-ATPase, Cu++ Transporting, alpha Polypeptide (ATP7A) (AA 42-61) antibody (Atto 594)ATP7A 适用: 人 WB, IHC, IP, IF, ICC 宿主: 小鼠 Monoclonal S60-4 Atto 594
anti-ATPase, Cu++ Transporting, alpha Polypeptide (ATP7A) (AA 42-61) antibody (Atto 390)ATP7A 适用: 人 WB, IHC, IP, IF, ICC 宿主: 小鼠 Monoclonal S60-4 Atto 390
anti-ATPase, Cu++ Transporting, alpha Polypeptide (ATP7A) (AA 242-285) antibodyATP7A 适用: 人, 大鼠, 小鼠 WB, ELISA, IHC (p), IF (p), IF (cc), IHC (fro) 宿主: 兔 Polyclonal unconjugated
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- 应用备注
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WB: 2.5 µg/mL
Optimal conditions should be determined by the investigator. - 限制
- 仅限研究用
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- 状态
- Lyophilized
- 溶解方式
- Lyophilized powder. Add distilled water for a 1 mg/mL concentration of ATP0 antibody in PBS
- 浓度
- Lot specific
- 缓冲液
- PBS
- 注意事项
- Avoid repeated freeze/thaw cycles.
- 储存条件
- 4 °C/-20 °C
- 储存方法
- Store at 2-8 °C for short periods. For longer periods of storage, store at -20 °C.
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- 抗原
- ATP7A (ATPase, Cu++ Transporting, alpha Polypeptide (ATP7A))
- 别名
- ATP7A (ATP7A 产品)
- 别名
- ATP7A antibody, cal antibody, wu:fc43e01 antibody, zgc:153422 antibody, zgc:158633 antibody, DDBDRAFT_0218568 antibody, DDBDRAFT_0235190 antibody, DDB_0218568 antibody, DDB_0235190 antibody, atpase antibody, Atp7a antibody, kal antibody, atp7a antibody, DSMAX antibody, MK antibody, MNK antibody, SMAX3 antibody, Blo antibody, DXHXS1608e antibody, I14 antibody, Mo antibody, blotchy antibody, br antibody, brindled antibody, mottled antibody, Mnk antibody, ATPase copper transporting alpha antibody, ATPase, Cu++ transporting, alpha polypeptide antibody, P-type ATPase antibody, ATP synthase subunit a antibody, copper-transporting ATPase 1 antibody, ATP7A antibody, atp7a antibody, LOC100049514 antibody, Atp7a antibody, LOC412379 antibody
- 背景
- The ATP7A gene encodes the Menkes copper-translocating P-type ATPase, a ubiquitous protein that regulates the absorption of copper in the gastrointestinal tract. Inside cells, this protein has a dual function: it delivers copper to cuproenzymes in the Golgi compartment and effluxes excess copper. The trafficking mechanism and catalytic activity combine to facilitate absorption and intercellular transport of copper. Menkes disease, a systemic copper deficiency disorder, is caused by mutations in the ATP7A gene.
- 分子量
- 30 kDa (MW of target protein)
- 途径
- Transition Metal Ion Homeostasis, Ribonucleoside Biosynthetic Process
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