TMEM248 Rabbit Polyclonal Antibody
cat.: ER1803-48
Product Type: Rabbit polyclonal IgG, primary antibodies
Species reactivity: Human, Rat, Mouse
Applications: WB, IF-Cell, FC
Clonality: Polyclonal
Form: Liquid
Storage condition: Shipped at 4℃. Store at +4℃ short term (1-2 weeks). It is recommended to aliquot into single-use upon delivery. Store at -20℃ long term.
Storage buffer: 1*PBS (pH7.4), 0.2% BSA, 50% Glycerol. Preservative: 0.05% Sodium Azide.
Concentration: 1ug/ul
Purification: Immunogen affinity purified.
Molecular weight: Predicted band size: 35 kDa
Isotype: IgG
Immunogen: Synthetic peptide within Human TMEM248 aa 265-314 / 314.
Positive control: K-562 cell lysate, SK-Br-3 cell lysate, A-172 cell lysate, HeLa cell lysate, PC-12 cell lysate, HUVEC, SH-SY-5Y, SiHa.
Subcellular location: Membrane.
Recommended Dilutions:
  WB
  IF-Cell
  FC

1:1,000-1:5,000
1:50-1:200
1:50-1:100
Uniprot #: SwissProt: Q9NWD8 Human | Q3TBN1 Mouse | Q6AY76 Rat
Alternative names: Transmembrane protein 248 TMEM248 C7orf42
Images
ER1803-48_1.jpg Fig1: Western blot analysis of TMEM248 on different lysates with Rabbit anti-TMEM248 antibody (ER1803-48) at 1/1,000 dilution.

Lane 1: K-562 cell lysate
Lane 2: SK-Br-3 cell lysate
Lane 3: A-172 cell lysate

Lysates/proteins at 10 µg/Lane.

Predicted band size: 35 kDa
Observed band size: 30 kDa

Exposure time: 1 minute 16 seconds; 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 (ER1803-48) 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.
ER1803-48_2.jpg Fig2: Western blot analysis of TMEM248 on different lysates with Rabbit anti-TMEM248 antibody (ER1803-48) at 1/5,000 dilution.

Lane 1: K-562 cell lysate (no heat)
Lane 2: HeLa cell lysate (hot lysis)
Lane 3: PC-12 cell lysate

Notice: no heat means the lysate is not boiled.

Lysates/proteins at 20 µg/Lane.

Predicted band size: 35 kDa
Observed band size: 30 kDa

Exposure time: 1 minute 16 seconds; 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 (ER1803-48) at 1/5,000 dilution was used in primary antibody dilution (K1803) at 4℃ overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1/50,000 dilution was used for 1 hour at room temperature.
ER1803-48_3.jpg Fig3: ICC staining Tmem248 in HUVEC cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.
ER1803-48_4.jpg Fig4: ICC staining Tmem248 in SH-SY-5Y cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.
ER1803-48_5.jpg Fig5: ICC staining Tmem248 in SiHa cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.
ER1803-48_6.jpg Fig6: Flow cytometric analysis of SH-SY-5Y cells with Tmem248 antibody at 1/100 dilution (red) compared with an unlabelled control (cells without incubation with primary antibody; green). Alexa Fluor 488-conjugated goat anti-rabbit IgG was used as the secondary antibody.
Note: All products are “FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE”.