What is the catalog number for Rabbit anti-ATP7B Antibody?

The catalog number for Rabbit anti-ATP7B Antibody is DL93574A.

What sizes are available for Rabbit anti-ATP7B Antibody?

Rabbit anti-ATP7B Antibody is available in the following size(s): 50 µL, 100 µL.

How many pack sizes does Rabbit anti-ATP7B Antibody come in?

Rabbit anti-ATP7B Antibody is available in 2 different pack sizes.

Is Rabbit anti-ATP7B Antibody in stock?

Rabbit anti-ATP7B Antibody is currently made to order / not held in immediate stock. Contact us for lead time.

Rabbit anti-ATP7B Antibody

Product Specifications

Background

Rabbit polyclonal antibody to ATP7B

CAS Number

9007-83-4

Synonyms

PWD; WC1; WND; Copper-transporting ATPase 2; Copper pump 2; Wilson disease-associated protein

Host

Rabbit

Reactivity

Immunogen

KLH-conjugated synthetic peptide encompassing a sequence within the N-term region of human ATP7B. The exact sequence is proprietary.

Clonality

Polyclonal

Applications

WB, IHC, IF/IC

Purification Method

The antibody was purified by immunogen affinity chromatography.

Concentration

1mg/mL

Dilution

WB (1/500 - 1/1000), IH (1/100 - 1/200), IF/IC (1/100 - 1/500)

Buffer

Liquid in 0.42% Potassium phosphate, 0.87% Sodium chloride, pH 7.3, 30% glycerol, and 0.01% sodium azide.

Storage Conditions

Store at -20°C. Avoid repeated freeze / thaw cycles.

WB Description

Western blot analysis of ATP7B expression in HepG2 (A), Human lung (B) whole cell lysates.

IHC description

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.

IF/ICC description

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) .