ATP7A (42-61, Cytopl. Dom.) Mouse Monoclonal Antibody [Clone ID: S60-4]

CAT#: AM60002PU-N

ATP7A (42-61, Cytopl. Dom.) mouse monoclonal antibody, clone S60-4, Purified



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CNY 5,742.00


货期*
4周

规格
    • 100 ug

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Specifications

Product Data
Clone Name S60-4
Applications IHC, IP, WB
Recommend Dilution Immunohistochemistry: free floating sections, fixed in formaldehyde.
Immunoprecipitation.
Western Blot:
1 μg/ml of this antibody was sufficient for detection of ATP7A / Copper-transporting ATPase1 in 20 μg of rat brain lysate by colorimetric immunoblot analysis using goat anti mouse IgG-HRP as the secondary antibody
Reactivity Human, Mouse, Rat
Host Mouse
Clonality Monoclonal
Immunogen Fusion protein amino acids 42-61 (cytoplasmic, C-terminus) of human ATP7A / Copper- transporting ATPase 1
Specificity This antibody detects ATP7A (aa42-61); ~180kDa.
Formulation PBS pH 7.2, 50% Glycerol
State: Purified
State: Liquid purified IgG fraction
Preservative: 0.09% Sodium azide
Concentration lot specific
Purification Protein G chromatography
Conjugation Unconjugated
Storage Condition Upon receipt, store undiluted (in aliquots) at -20°C.
Avoid repeated freezing and thawing.
Gene Name ATPase copper transporting alpha
Background The copper efflux transporters ATP7A and ATP7B sequester intracellular copper into the vesicular secretory pathway for export from the cell. ATP7A (also known as Copper-transporting ATPase 1) functions as a transmembrane copper-translocating P-type ATPase and plays a vital role in systemic copper absorption in the gut and copper reabsorption in the kidney. Polarized epithelial cells such as Madin-Darby canine kidney cells are a physiologically relevant model for systemic copper absorption and reabsorption in vivo. Although ATP7A is not detectable in most normal tissues, it is expressed in a considerable fraction of many common tumor types. Increased expression of ATP7A renders cells resistant to cisplatin and carboplatin. Mutations in the ATP7A gene result in Menkes disease, which is fatal in early childhood. Mutations in the ATP7B gene lead to the autosomal recessive disorder, Wilson disease, characterized by neurological symptoms and hepatic damage.
Synonyms Copper pump 1, MC1, MNK
Reference Data
*Delivery time may vary from web posted schedule. Occasional delays may occur due to unforeseen complexities in the preparation of your product. International customers may expect an additional 1-2 weeks in shipping.
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