Neuronatin Recombinant Rabbit Monoclonal Antibody [JE35-00]
cat.: HA722326
Product Type: Recombinant Rabbit monoclonal IgG, primary antibodies
Species reactivity: Human, Mouse, Rat
Applications: WB, IHC-P
Clonality: Monoclonal
Clone number: JE35-00
Form: Liquid
Storage condition: Store at +4℃ after thawing. Aliquot store at -20℃. Avoid repeated freeze / thaw cycles.
Storage buffer: 1*TBS (pH7.4), 0.05% BSA, 40% Glycerol. Preservative: 0.05% Sodium Azide.
Concentration: 1ug/ul
Purification: Protein A affinity purified.
Molecular weight: Predicted band size: 9 kDa
Isotype: IgG
Immunogen: Synthetic peptide within Human Neuronatin aa 32-81 / 81.
Positive control: SH-SY5Y cell lysate, E14.0 mouse brain tissue lysate, mouse embryo tissue lysate, rat embryo tissue lysate, human brain tissue.
Subcellular location: Cytoplasm.
Recommended Dilutions:
  WB
  IHC-P

1:1,000
1:200
Uniprot #: SwissProt: Q16517 Human | Q61979 Mouse | Q62649 Rat
Alternative names: Neuronatin NNAT NNAT_HUMAN Peg 5 Peg5
Images
HA722326_1.jpg Fig1: Western blot analysis of Neuronatin on different lysates with Rabbit anti-Neuronatin antibody (HA722326) at 1/1,000 dilution.

Lane 1: SH-SY5Y cell lysate
Lane 2: SK-Br-3 cell lysate (negative)
Lane 3: E14.0 mouse brain tissue lysate
Lane 4: Mouse embryo tissue lysate
Lane 5: Rat embryo tissue lysate

Lysates/proteins at 20 µg/Lane.

Predicted band size: 9 kDa
Observed band size: 12 kDa

Exposure time: 3 minutes; ECL: K1801;

4-20% SDS-PAGE gel.

Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (HA722326) at 1/1,000 dilution was used in 5% NFDM/TBST at 4℃ overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1/50,000 dilution was used for 1 hour at room temperature.
HA722326_2.jpg Fig2: Immunohistochemical analysis of paraffin-embedded human brain tissue with Rabbit anti-Neuronatin antibody (HA722326) at 1/200 dilution.

The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (HA722326) at 1/200 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.
Note: All products are “FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE”.