ATP7A 抗体 (Middle Region)
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- 抗原 See all ATP7A 抗体
- ATP7A (ATPase, Cu++ Transporting, alpha Polypeptide (ATP7A))
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抗原表位
- Middle Region
- 适用
- 人, 大鼠, 小鼠, 犬, Cow, 马, 豚鼠, 兔, 绵羊, Saccharomyces cerevisiae, 斑马鱼
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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)
- 序列
- MGSAAMAASS VSVVLSSLFL KLYRKPTYES YELPARSQIG QKSPSEISVH
- 预测反应
- Cow: 100%, Dog: 100%, Guinea Pig: 100%, Horse: 93%, Human: 100%, Mouse: 100%, Rabbit: 100%, Rat: 100%, Sheep: 100%, Yeast: 93%, Zebrafish: 92%
- 产品特性
- This is a rabbit polyclonal antibody against ATP7A. It was validated on Western Blot.
- 纯化方法
- Affinity Purified
- 免疫原
- The immunogen is a synthetic peptide directed towards the middle region of Human ATP7A
- 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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- 限制
- 仅限研究用
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- 状态
- Liquid
- 浓度
- 1 mg/mL
- 缓冲液
- Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
- 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 repeat freeze-thaw cycles.
- 储存条件
- -20 °C
- 储存方法
- For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
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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
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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.
Protein Interaction Partner: ACIN1, UBC, COMMD1, CLU, ATOX1, PDZD11, CP, GLRX,
Protein Size: 503 - 分子量
- 55 kDa
- 基因ID
- 538
- 途径
- Transition Metal Ion Homeostasis, Ribonucleoside Biosynthetic Process
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