What is the catalog number for Rabbit anti-NAT13 Antibody?

The catalog number for Rabbit anti-NAT13 Antibody is DL96450A.

What sizes are available for Rabbit anti-NAT13 Antibody?

Rabbit anti-NAT13 Antibody is available in the following size(s): 50 µL, 100 µL.

How many pack sizes does Rabbit anti-NAT13 Antibody come in?

Rabbit anti-NAT13 Antibody is available in 2 different pack sizes.

Is Rabbit anti-NAT13 Antibody in stock?

Rabbit anti-NAT13 Antibody is currently made to order / not held in immediate stock. Contact us for lead time.

Rabbit anti-NAT13 Antibody

Product Specifications

Background

Rabbit polyclonal antibody to NAT13

CAS Number

9007-83-4

Synonyms

MAK3; NAT13; NAT5; N-alpha-acetyltransferase 50; N-acetyltransferase 13; N-acetyltransferase 5; hNAT5; N-acetyltransferase san homolog; hSAN; NatE catalytic subunit

Host

Rabbit

Reactivity

H, M, R

Immunogen

Recombinant full length protein of human NAT13

Clonality

Polyclonal

Applications

WB, IHC, IF/IC

Purification Method

The antibody was purified by immunogen affinity chromatography.

Concentration

1mg/mL

Dilution

WB (1/500 - 1/2000), IH (1/50 - 1/200), IF/IC (1/50 - 1/200)

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 NAT13 expression in SKOV3 (A), MCF7 (B), mouse brain (C) whole cell lysates.

IHC description

Immunohistochemical analysis of NAT13 staining in rat kidney 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 NAT13 staining in A549 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.