Product Type: | Recombinant Rabbit monoclonal IgG, primary antibodies |
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Species reactivity: | Human, Rat |
Applications: | WB, IF-Cell, FC |
Clonality: | Monoclonal |
Clone number: | PSH0-40 |
Form: | Liquid |
Storage condition: | Store at +4℃ after thawing. Aliquot store at -20℃. Avoid repeated freeze / thaw cycles. |
Storage buffer: | PBS (pH7.4), 0.1% BSA, 40% Glycerol. Preservative: 0.05% Sodium Azide. |
Concentration: | 1ug/ul |
Purification: | Protein A affinity purified. |
Molecular weight: | Predicted band size: 112.6 kDa |
Isotype: | IgG |
Immunogen: | Recombinant protein within human RTN3 aa 1-500 / 1,032. |
Positive control: | HeLa cell lysate, HEK-293 cell lysate, U87-MG cell lysate, A549 cell lysate, SH-SY5Y cell lysate, PC-12 cell lysate, L6 cell lysate, human cerebellum tissue lysate, PC-12, HeLa. |
Subcellular location: | Endoplasmic reticulum membrane, Golgi apparatus membrane. |
Recommended Dilutions:
WB IF-Cell FC |
1:1,000 1:50 1:500-1:1,000 |
Uniprot #: | SwissProt: O95197 Human | Q6RJR6 Rat |
Alternative names: | ASYIP Neuroendocrine specific protein like 2 Neuroendocrine-specific protein-like 2 Neuroendocrine-specific protein-like II NSP like protein II NSP-like protein 2 NSP-like protein II NSPL2 NSPLII Reticulon 3 Reticulon-3 Reticulon3 Rtn3 RTN3_HUMAN |
Fig1:
Western blot analysis of RTN3 on different lysates with Rabbit anti-RTN3 antibody (HA721342) at 1/1,000 dilution. Lane 1: HeLa cell lysate (32 µg/Lane) Lane 2: HEK-293 cell lysate (33 µg/Lane) Lane 3: U87-MG cell lysate (30 µg/Lane) Lane 4: A549 cell lysate (26 µg/Lane) Lane 5: SH-SY5Y cell lysate (18 µg/Lane) Lane 6: PC-12 cell lysate (23 µg/Lane) Lane 7: L6 cell lysate (14 µg/Lane) Lane 8: Human cerebellum tissue lysate (40 µg/Lane) Lysates/proteins at 10 µg/Lane. Predicted band size: 112.6 kDa Observed band size: 100 kDa Exposure time: 3 minutes; 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 (HA721342) at 1/1,000 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1:200,000 dilution was used for 1 hour at room temperature. |
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Fig2:
Immunocytochemistry analysis of PC-12 cells labeling RTN3 with Rabbit anti-RTN3 antibody (HA721342) at 1/50 dilution. Cells were fixed in 4% paraformaldehyde for 10 minutes at 37 ℃, permeabilized with 0.05% Triton X-100 in PBS for 20 minutes, and then blocked with 2% negative goat serum for 30 minutes at room temperature. Cells were then incubated with Rabbit anti-RTN3 antibody (HA721342) at 1/50 dilution in 2% negative goat serum overnight at 4 ℃. Goat Anti-Rabbit IgG H&L (iFluor™ 488, HA1121) was used as the secondary antibody at 1/1,000 dilution. Nuclear DNA was labelled in blue with DAPI. Beta tubulin (M1305-2, red) was stained at 1/100 dilution overnight at +4℃. Goat Anti-Mouse IgG H&L (iFluor™ 594, HA1126) was used as the secondary antibody at 1/1,000 dilution. |
Fig3:
Flow cytometric analysis of HeLa cells labeling RTN3. Cells were fixed and permeabilized. Then stained with the primary antibody (HA721342, 1ug/ml) (red) compared with Rabbit IgG Isotype Control (green). After incubation of the primary antibody at +4℃ for an hour, the cells were stained with a iFluor™ 488 conjugate-Goat anti-Rabbit IgG Secondary antibody (HA1121) at 1/1,000 dilution for 30 minutes at +4℃. Unlabelled sample was used as a control (cells without incubation with primary antibody; black). |