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ATP7A 抗体
ATP7A
适用: 人, 大鼠
IHC
宿主: 兔
Polyclonal
unconjugated
ATP7A抗体详情
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抗原
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ATP7A
(ATPase, Cu++ Transporting, alpha Polypeptide (ATP7A))
适用
All reactivities for ATP7A 抗体
人, 大鼠
宿主
All hosts for ATP7A 抗体
兔
克隆类型
All clonalities for ATP7A 抗体
多克隆
标记
All conjugates for ATP7A 抗体
This ATP7A antibody is un-conjugated
应用范围
All applications for ATP7A 抗体
Immunohistochemistry (IHC)
产品特性
Polyclonal Antibody
纯化方法
Affinity purification
免疫原
Recombinant fusion protein of human ATP7A (NP_000043.4).
亚型
IgG
Top Product
Discover our top product ATP7A Primary Antibody
Alternatives
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使用细节
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应用备注
IHC 1:50-1:100
限制
仅限研究用
贮存及处理
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状态
Liquid
浓度
1 mg/mL
缓冲液
PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
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
-20 °C
储存方法
Store at -20°C. Avoid freeze / thaw cycles.
ATP7A目标详情
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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
This gene encodes a transmembrane protein that functions in copper transport across membranes. This protein is localized to the trans Golgi network, where it is predicted to supply copper to copper-dependent enzymes in the secretory pathway. It relocalizes to the plasma membrane under conditions of elevated extracellular copper, and functions in the efflux of copper from cells. Mutations in this gene are associated with Menkes disease, X-linked distal spinal muscular atrophy, and occipital horn syndrome. Alternatively-spliced transcript variants have been observed.
基因ID
538
UniProt
Q04656
途径
Transition Metal Ion Homeostasis , Ribonucleoside Biosynthetic Process
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