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ATP7B Antibody, Clone L62/29

Mouse Anti-Human ATP7B (Copper Transporting ATPase 2) Monoclonal IgG1

Product Specifications

Background

ATP7B is a copper-transporting P-type ATPase critical for maintaining systemic and neuronal copper balance. Working in tandem with ATP7A, ATP7B facilitates the sequestration of intracellular copper into the vesicular secretory pathway, enabling its export and preventing toxic accumulation. This function is essential for copper detoxification, particularly in the liver, where ATP7B mediates biliary copper excretion. ATP7B operates by using ATP hydrolysis to transport copper ions across cellular membranes. Three isoforms of the ATP7B gene have been identified: isoform A is expressed in the liver, kidney, and brain; isoform B is brain-specific; and the WND/140 kDa isoform localizes to mitochondria, suggesting a role in mitochondrial copper regulation and oxidative stress response. Mutations in ATP7B cause Wilson disease, a rare autosomal recessive disorder characterized by copper accumulation in the liver and brain. Neurological manifestations include tremors, dystonia, psychiatric disturbances, and cognitive decline—highlighting the protein’s importance in neural function and copper detoxification. In neuroscience, ATP7B is increasingly recognized for its role in protecting neurons from copper-induced oxidative damage, a contributing factor in neurodegenerative diseases such as Alzheimer’s and Parkinson’s. Dysregulation of ATP7B may exacerbate mitochondrial dysfunction and protein aggregation, linking copper imbalance to broader neurodegenerative mechanisms. As a key regulator of copper metabolism, ATP7B represents a promising target for therapeutic strategies aimed at restoring metal homeostasis in neurodegenerative disease.

CAS Number

9007-83-4

Specifications

Detects ~160kDa in rat brain membrane preparations.

Product Name Alternative

ATP7B, ATPase Cu++ transporting beta polypeptide, ATPase Cu (2+) transporting beta polypeptide, Copper pump 2, Copper transporting ATPase 2, PWD, Toxic milk, tx, WC1, WD, Wilson disease associated protein, WND, WND/140 kDa

Synonyms

Copper Transporting ATPase 2 Antibody, Clone L62/29

UNSPSC

12352203

UN Code

Non-hazardous

Hazard Statement

Non-hazardous

Gene ID

540

Swiss Prot

B7ZLR4

Accession Number

NP_000044.2

Cellular Locus

Cytoplasm | Mitochondrion | Golgi Apparatus | Trans-Golgi Network Membrane

Host

Mouse

Species Reactivity

Human,Mouse,Rat

Immunogen

Synthetic peptide amino acids 3-21 (cytoplasmic N-terminus) of human Copper-transporting ATPase2

Target

ATP7B

Clonality

Monoclonal

Isotype

IgG1

Clone

L62/29 (Formerly sold as S62-29)

Conjugation

Unconjugated

Type

Monoclonal

Applications

WB | IHC | ICC/IF | IP

Validated Applications

WB,IHC,ICC/IF,IP

Field of Research

Neuroscience | Ion Channels | Cell Signaling

Purification

Protein G Purified

Limit Of Detection

1 µg/ml of SMC-399 was sufficient for detection of Copper-transporting ATPase2 in 20 µg of rat brain lysate by colorimetric immunoblot analysis using Goat IgG:HRP as the secondary antibody.

Concentration

1 mg/ml

Dilution

WB (1:1000), ICC/IF (1:100) ; optimal dilutions for assays should be determined by the user.

Weight

0.1

Buffer

PBS pH7.4, 50% glycerol, 0.09% sodium azide *Storage buffer changes when conjugated

Precautions

Not for use in humans. Not for use in diagnostics or therapeutics. For in vitro research use only.

References & Citations

1. Tanzi R.E., et al. (1993) Nature Genetics. 5: 344-350. 2. Ghr/nlm.gov/gene/ATP7B

Shipping Conditions

Blue Ice or 4ºC

Storage Conditions

-20ºC

Specificity

Detects ~160kDa in rat brain membrane preparations.

Background Reference 01

1. Tanzi R.E., et al. (1993) Nature Genetics. 5: 344-350. 2. Ghr/nlm.gov/gene/ATP7B

Species

Human | Mouse | Rat

Location

Cytoplasm | Mitochondrion | Golgi Apparatus | Trans-Golgi Network Membrane

Isotype

IgG1

Immunogen Species

Human

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