Involved in nuclear membrane organization. Predicted to be located in nuclear inner membrane. Predicted to be integral component of membrane. Predicted to be active in nuclear envelope. Together with EMD, contributes to nuclear envelope stiffness in germ cells. Required for female fertility (By similarity).
Background References
1. Hodzic D et al. he inner nuclear membrane protein NEMP1 supports nuclear envelope openings and enucleation of erythroblasts. PLoS Biol. 2022 Oct
2. Liu Y et al. NEMP1 Promotes Tamoxifen Resistance in Breast Cancer Cells. Biochem Genet. 2019 Dec
Western blot analysis of NEMP1 on different lysates with Rabbit anti-NEMP1 antibody (HA722738) at 1/1,000 dilution.
Lane 1: Mouse spleen tissue lysate (no heat) Lane 2: Mouse skin tissue lysate (hot lysis) Lane 3: Mouse placenta tissue lysate (70℃ heat) Lane 4: Rat spleen tissue lysate (no heat) Lane 5: Rat skin tissue lysate (hot lysis)
Notice: no heat means the lysate is not boiled.
Lysates/proteins at 40 µg/Lane.
Predicted band size: 50 kDa Observed band size: 50 kDa
Exposure time: 2 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 (HA722738) 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.
☑ Cell treatment (CT)
Immunocytochemistry analysis of HeLa transfected with or without mouse NEMP1 cells labeling NEMP1 with Rabbit anti-NEMP1 antibody (HA722738) at 1/100 dilution.
Cells were fixed in 4% paraformaldehyde for 20 minutes at room temperature, permeabilized with 0.1% Triton X-100 in PBS for 5 minutes at room temperature, then blocked with 1% BSA in 10% negative goat serum for 1 hour at room temperature. Cells were then incubated with Rabbit anti-NEMP1 antibody (HA722738) at 1/100 dilution in 1% BSA in PBST overnight at 4 ℃. Goat Anti-Rabbit IgG H&L (iFluor™ 488, HA1121) was used as the secondary antibody at 1/1,000 dilution. PBS instead of the primary antibody was used as the secondary antibody only control. 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.
Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"