ATP7B Polyclonal Antibody, DyLight™ 488, Invitrogen™
Manufacturer: Thermo Scientific
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | PIPA522769-Each-of-1 | In Stock | ₹ 46,591.50 |
PIPA522769 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 46,591.50
GST (18%): ₹ 8,386.47
Total Price: ₹ 54,977.97
Antigen
ATP7B
Classification
Polyclonal
Conjugate
DyLight 488
Gene
Atp7b
Gene Alias
Atp7a; ATP7B; ATPase copper transporting beta; ATPase, Cu(2+)- transporting, beta polypeptide; ATPase, Cu++ transporting, beta polypeptide; ATPase, Cu++ transporting, beta polypeptide (same as Wilson disease); copper pump 2; Copper-transporting ATPase 2; Hts; PINA; PINA gene, promoter; pineal night-specific ATPase; PWD; RP11-327P2.1; RP11-327P2.3; toxic milk; tx; WC1; WD; Wilson disease-associated protein; wilson disease-associated protein homolog; Wilson protein; Wnd; WND/140 kDa
Host Species
Rabbit
Purification Method
Antigen affinity chromatography
Regulatory Status
RUO
Gene ID (Entrez)
24218, 540
Content And Storage
4° C, store in dark
Form
Liquid
Applications
Immunocytochemistry, Western Blot
Concentration
0.93 mg/mL
Formulation
50mM sodium borate with 0.05% sodium azide
Gene Accession No.
P35670, Q64535
Gene Symbols
Atp7b
Immunogen
A synthetic peptide made to an internal sequence nearer the C-terminus of human ATP7b.
Quantity
100 μL
Primary or Secondary
Primary
Target Species
Human, Rat
Product Type
Antibody
Isotype
IgG
Related Products
Description
- This antibody does not react with mouse samples
- This gene is a member of the P-type cation transport ATPase family and encodes a protein with several membrane-spanning domains, an ATPase consensus sequence, a hinge domain, a phosphorylation site, and at least 2 putative copper-binding sites
- This protein functions as a monomer, exporting copper out of the cells, such as the efflux of hepatic copper into the bile
- Alternate transcriptional splice variants, encoding different isoforms with distinct cellular localizations, have been characterized
- Mutations in this gene have been associated with Wilson disease (WD).