Products for Research Use Only

ATP7B Antibody (C-term)

CAT: 0013-GTR18327415Size: 400 µLDry Ice: NoHazardous: No
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CAT#:0013-GTR18327415Size:400 µL
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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Description
Purified Rabbit Polyclonal Antibody (Pab)
Product Name Alternative
Copper-transporting ATPase 2, Copper pump 2, Wilson disease-associated protein, WND/140 kDa, ATP7B, PWD, WC1, WND
UniProt
P35670
Reactivity
Human, Mouse
Immunogen
This ATP7B antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 1361-1391 amino acids from the C-terminal region of human ATP7B. Antigen Region: 1361-1391 aa.
Target
ATP7B
Clonality
Polyclonal
Conjugation
Unconjugated
Field of Research
Cancer Biology
Dilution
WB - 1:2000, IF - 1:10-50, IHC-P - 1:10-50, FC - 1:10-50
Form
Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein A column, followed by peptide affinity purification.
Molecular Weight
157263 Da
Storage Conditions
Maintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles
Notes
For research use only.
Tested Applications
FC, IF, IHC-P, WB
NCBI Accession Number
NP_001230111.1, NP_000044.2
Host or Source
Rabbit
Isotype
Rabbit IgG

UniProtKB · P35670

Copper-transporting ATPase 2

ATP7B_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
P35670
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
ATP7B
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
—
EC number
7.2.2.8
Processing
—
Secondary accessions
Q16318, Q16319, Q4U3V3, Q59FJ9, Q5T7X7
Protein keywords

Technical term

3D-structureProteomics identificationReference proteome

Coding sequence diversity

Alternative splicingRibosomal frameshifting

Ligand

ATP-bindingCopperMagnesiumMetal-bindingNucleotide-binding

Biological process

Copper transportIon transportTransport

Cellular component

CytoplasmEndosomeGolgi apparatusMembraneMitochondrion

Disease

Disease variant

PTM

Phosphoprotein

Domain

RepeatTransmembraneTransmembrane helix

Molecular function

Translocase