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ATP7B, Polyclonal Antibody

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ATP7B, Polyclonal Antibody


ATP7B, Polyclonal Antibody  的詳細(xì)介紹
Product Name

ATP7B, Polyclonal Antibody

Full Product Name

Anti-ATP7B Antibody

Product Synonym Names
PWD; WC1; WND; Copper-transporting ATPase 2; Copper pump 2; Wilson disease-associated protein
Product Gene Name

anti-ATP7B antibody

[Similar Products]
Antibody/Peptide Pairs
ATP7B peptide (MBS8243519) is used for blocking the activity of ATP7B antibody (MBS8242766)
Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
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OMIM
277900
3D Structure
ModBase 3D Structure for P35670
Clonality
Polyclonal
Host
Rabbit
Species Reactivity
Human
Specificity
Recognizes endogenous levels of ATP7B protein.
Purity/Purification
The antibody was purified by immunogen affinity chromatography.
Form/Format
Liquid in 0.42% Potassium Phosphate, 0.87% Sodium Chloride, pH 7.3, 30% Glycerol, and 0.01% Sodium Azide.
Immunogen
KLH-conjugated synthetic peptide encompassing a sequence within the N-term region of human ATP7B. The exact sequence is proprietary.
Preparation and Storage
Shipped and store at 4 degree C for one year. Do not freeze.
Other Notes
Small volumes of anti-ATP7B antibody vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.
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Related Product Information for
anti-ATP7B antibody
Rabbit polyclonal antibody to ATP7B
Applications Tested/Suitable for anti-ATP7B antibody
Western Blot (WB), Immunohistochemistry (IHC), Immunofluorescence (IF), Immunocytochemistry (ICC)
Application Notes for anti-ATP7B antibody
Western Blot: (1/500 - 1/1000); Immunohistochemistry: (1/100 - 1/200); Immunofluorescence/Immunocytochemistry: (1/100 - 1/500)

Western Blot (WB) of anti-ATP7B antibody
Western blot analysis of ATP7B expression in HepG2 (A), Human lung (B) whole cell lysates.
anti-ATP7B antibody Western Blot (WB) (WB) image
Immunohistochemistry (IHC) of anti-ATP7B antibody
Immunohistochemical analysis of ATP7B staining in human breast cancer formalin fixed paraffin embedded tissue section. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0). The section was then incubated with the antibody at room temperature and detected using an HRP conjugated compact polymer system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX.
anti-ATP7B antibody Immunohistochemistry (IHC) (IHC) image
Immunofluorescence (IF) of anti-ATP7B antibody
Immunofluorescent analysis of ATP7B staining in HepG2 cells. Formalin-fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 5-10 minutes and blocked with 3% BSA-PBS for 30 minutes at room temperature. Cells were probed with the primary antibody in 3% BSA-PBS and incubated overnight at 4 °C in a humidified chamber. Cells were washed with PBST and incubated with a DyLight 594-conjugated secondary antibody (red) in PBS at room temperature in the dark. DAPI was used to stain the cell nuclei (blue).
anti-ATP7B antibody Immunofluorescence (IF) image
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NCBI/Uniprot data below describe general gene information for ATP7B. It may not necessarily be applicable to this product.
NCBI GI #
239938919
NCBI GeneID
540
NCBI Accession #
P35670.4 [Other Products]
UniProt Primary Accession #
P35670 [Other Products]
UniProt Secondary Accession #
Q16318; Q16319; Q4U3V3; Q59FJ9; Q5T7X7[Other Products]
UniProt Related Accession #
P35670[Other Products]
Molecular Weight
155,125 Da
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NCBI Official Full Name
Copper-transporting ATPase 2
NCBI Official Synonym Full Names
ATPase copper transporting beta
NCBI Official Symbol
ATP7B??[Similar Products]
NCBI Official Synonym Symbols
WD; PWD; WC1; WND
??[Similar Products]
NCBI Protein Information
copper-transporting ATPase 2
UniProt Protein Name
Copper-transporting ATPase 2
UniProt Synonym Protein Names
Copper pump 2; Wilson disease-associated protein
UniProt Gene Name
ATP7B??[Similar Products]
UniProt Synonym Gene Names
PWD; WC1; WND??[Similar Products]
UniProt Entry Name
ATP7B_HUMAN
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NCBI Summary for ATP7B
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-s. 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). [provided by RefSeq, Jul 2008]
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UniProt Comments for ATP7B
ATP7B: Involved in the export of copper out of the cells, such as the efflux of hepatic copper into the bile. Monomer. Interacts with COMMD1/MURR1. Most abundant in liver and kidney and also found in brain. Isoform 2 is expressed in brain but not in liver. The cleaved form WND/140 kDa is found in liver cell lines and other tissues. Belongs to the cation transport ATPase (P-type) (TC 3.A.3) family. Type IB subfamily. 4 isoforms of the human protein are produced by alternative splicing.

Protein type: Hydrolase; Membrane protein, multi-pass; Transporter; Membrane protein, integral; Vesicle; EC 3.6.3.54; Transporter, ion channel

Chromosomal Location of Human Ortholog: 13q14.3

Cellular Component: basolateral plasma membrane; cytoplasmic membrane-bound vesicle; Golgi membrane; integral to plasma membrane; late endosome; membrane; mitochondrion; perinuclear region of cytoplasm; tight junction; trans-Golgi network

Molecular Function: ATP binding; copper ion binding; copper-exporting ATPase activity; protein binding; zinc ion binding

Biological Process: cellular copper ion homeostasis; cellular zinc ion homeostasis; circadian rhythm; copper ion export; copper ion import; copper ion transport; intracellular copper ion transport; lactation; metabolic process; response to cAMP; response to copper ion; response to zinc ion; sequestering of calcium ion; transmembrane transport

Disease: Wilson Disease
Research Articles on ATP7B
1. Wilson disease causing p.T788I, p.V1036I and p.R1038G-fsX83 mutations lead to functional deficiency in ATP7B protein.
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Precautions
All of MyBioSource's Products are for scientific laboratory research purposes and are not for diagnostic, therapeutics, prophylactic or in vivo use. Through your purchase, you expressly represent and warrant to MyBioSource that you will properly test and use any Products purchased from MyBioSource in accordance with industry standards. MyBioSource and its authorized distributors reserve the right to refuse to process any order where we reasonably believe that the intended use will fall outside of our acceptable guidelines.
Disclaimer
While every efforts were made to ensure the accuracy of the information provided in this datasheet, MyBioSource will not be liable for any omissions or errors contained herein. MyBioSource reserves the right to make changes to this datasheet at any time without prior notice.

It is the responsibility of the customer to report product performance issues to MyBioSource within 30 days of receipt of the product. Please visit our Terms & Conditions page for more information.
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