CYP7A1 Rabbit Polyclonal Antibody
cat.: HA500207
Product Type: Rabbit polyclonal IgG, primary antibodies
Species reactivity: Human, Rat
Applications: WB, IF-Cell, FC
Clonality: Polyclonal
Form: Liquid
Storage condition: Store at +4℃ after thawing. Aliquot store at -20℃. Avoid repeated freeze / thaw cycles.
Storage buffer: 1*TBS (pH7.4), 0.2% BSA, 50% Glycerol. Preservative: 0.05% Sodium Azide.
Concentration: 1ug/ul
Purification: Immunogen affinity purified.
Molecular weight: Predicted band size: 58 kDa
Isotype: IgG
Immunogen: Recombinant protein within human CYP7A1 aa 50-250.
Positive control: LO2 cell lysate, Huh7 cell lysate, Hepa1-6 cell lysate, rat liver tissue lysate, SiHa, HeLa.
Subcellular location: Endoplasmic reticulum membrane, Microsome membrane.
Recommended Dilutions:
  WB
  IF-Cell
  FC

1:1,000
1:200
1:200-1:500
Uniprot #: SwissProt: P22680 Human | P18125 Rat
Alternative names: Cholesterol 7 alpha hydroxylase Cholesterol 7 alpha monooxygenase Cholesterol 7-alpha-hydroxylase Cholesterol 7-alpha-monooxygenase CP7A CP7A1_HUMAN CYP 7 CYP7 CYP7A1 CYPVII Cytochrome P450 7A1 Cytochrome P450, family 7, subfamily A, polypeptide 1 Cytochrome P450, subfamily VIIA (cholesterol 7 alpha monooxygenase), Cytochrome P450, subfamily VIIA (cholesterol 7 alpha-monooxygenase), polypeptide 1 MGC126826 MGC138389
Images
HA500207_1.jpg Fig1: Western blot analysis of CYP7A1 on different lysates with Rabbit anti-CYP7A1 antibody (HA500207) at 1/1,000 dilution.

Lane 1: LO2 cell lysate
Lane 2: Huh7 cell lysate
Lane 3: Hepa1-6 cell lysate
Lane 4: Rat liver tissue lysate

Lysates/proteins at 20 µg/Lane.

Predicted band size: 58 kDa
Observed band size: 58 kDa

Exposure time: 1 minute 50 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 (HA500207) 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.
HA500207_2.jpg Fig2: Immunocytochemistry analysis of SiHa cells labeling CYP7A1 with Rabbit anti-CYP7A1 antibody (HA500207) at 1/200 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-CYP7A1 antibody (HA500207) at 1/200 dilution in 2% negative goat serum overnight at 4 ℃. Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) 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 1/200 dilution overnight at +4℃. Goat Anti-Mouse IgG H&L (Alexa Fluor® 647) were used as the secondary antibody at 1/1,000 dilution.
HA500207_3.jpg Fig3: Flow cytometric analysis of CYP7A1 was done on HeLa cells. The cells were fixed, permeabilized and stained with the primary antibody (HA500207, 1ug/ml) (red) compared with Rabbit IgG, monoclonal - Isotype Control (green). After incubation of the primary antibody at +4℃ for 1 hour, the cells were stained with a Alexa Fluor®488 conjugate-Goat anti-Rabbit IgG Secondary antibody at 1/1,000 dilution for 30 minutes at +4℃ (dark incubation).Unlabelled sample was used as a control (cells without incubation with primary antibody; black).
Note: All products are “FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE”.