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Read our guarantee »Products:Cardiovascular >> Lipids / Lipoproteins >> Lipid Metabolism >> Cholesterol Metabolism
Anti-SREBP2 antibody
See all SREBP2 products (4) ...
Rabbit polyclonal to SREBP2
Under basal conditions SREBP is bound to ER membranes as a glycosylated precursor protein. Upon cholesterol depletion, the protein is cleaved to its active forms (50-68 kDa) and translocated into the nucleus to stimulate transcription of genes involved in the uptake and synthesis of cholesterol. ab30682 detects both precursor and active forms of SREBP2 in tissues and cells such as liver, brown fat, testis, HepG2 cells, and human fibroblast. The apparent molecular weight on SDS-PAGE may be higher than the calculated molecular weight (about 126 kDa) due to glycosylation of the protein.
IHC-Fr, WB, ICCmore details
Reacts with
Mouse, Rat, Chicken, Human
Predicted to work with
Pig, Xenopus laevis, Chinese Hamster
Synthetic peptide: SPLLDDAKVKDEPDS, corresponding to amino acids 455 - 469 of Human SREBP2
SPLLDDAKVK DEPDS
Rat testis supernatant.
Liquid
Shipped at 4°C. Upon delivery aliquot and store at -20°C. Avoid freeze / thaw cycles.
Preservative: 0.02% Sodium Azide
Constituents: 50% Glycerol, 0.1% BSA, Tris buffered saline. pH 7.4
Concentration information loading...
Immunogen affinity purified
Polyclonal
IgG
Cancer >> Cancer Metabolism >> Metabolic signaling pathway >> Metabolism of lipids and lipoproteins
Epigenetics and Nuclear Signaling >> Transcription >> Transcription Factors
Epigenetics and Nuclear Signaling >> Transcription >> Domain Families >> HLH / Leucine Zipper >> HLH / Leucine Zipper
Cardiovascular >> Lipids / Lipoproteins >> Lipid Metabolism >> Cholesterol Metabolism
Our Abpromise guarantee covers the use of ab30682 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
IHC-Fr: 1/100
WB: Use a concentration of 4 µg/mlDetects a band of approximately 126 kDa (predicted molecular weight: 126 kDa).(Block with 0.5% non-fat dry milk in TBS pH 7.4 for 1-2 hours at room temperature or over night at 4 °C.)
ICC: Use a concentration of 4 µg/ml
Transcriptional activator required for lipid homeostasis. Regulates transcription of the LDL receptor gene as well as the cholesterol and to a lesser degree the fatty acid synthesis pathway (By similarity). Binds the sterol regulatory element 1 (SRE-1) (5'-ATCACCCCAC-3') found in the flanking region of the LDRL and HMG-CoA synthase genes.
Ubiquitously expressed in adult and fetal tissues.
Belongs to the SREBP family.
Contains 1 basic helix-loop-helix (bHLH) domain.
At low cholesterol the SCAP/SREBP complex is recruited into COPII vesicles for export from the ER. In the Golgi complex SREBPs are cleaved sequentially by site-1 and site-2 protease. The first cleavage by site-1 protease occurs within the luminal loop, the second cleavage by site-2 protease occurs within the first transmembrane domain and releases the transcription factor from the Golgi membrane. Apoptosis triggers cleavage by the cysteine proteases caspase-3 and caspase-7.
Nucleus and Endoplasmic reticulum membrane. Golgi apparatus membrane. Cytoplasmic vesicle > COPII-coated vesicle membrane. Moves from the endoplasmic reticulum to the Golgi in the absence of sterols.
Target information above from: UniProt accessionQ12772
The UniProt Consortium
The Universal Protein Resource (UniProt) in 2010
Nucleic Acids Res. 38:D142-D148 (2010).
Western blot - SREBP2 antibody (ab30682)

All lanes : Anti-SREBP2 antibody (ab30682) at 2.5 µg/ml
Lane 1 : Human fibroblast cell lysate
Lane 2 : Rat brown fat homogenate
Lane 3 : Rat testis supernatant
Lysates/proteins at 60 µg per lane.
Predicted band size : 126 kDa
Observed bands 126 kDa, 55kDa (cleaved form)
Immunocytochemistry/ Immunofluorescence - SREBP2 antibody (ab30682)

ICC/IF image of ab30682 stained HeLa cells. The cells were 4% PFA fixed (10 min) and then incubated in 1%BSA / 10% normal goat serum / 0.3M glycine in 0.1% PBS-Tween for 1h to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody (ab30682, 1µg/ml) overnight at +4°C. The secondary antibody (green) was Alexa Fluor® 488 goat anti-rabbit IgG (H+L) used at a 1/1000 dilution for 1h. Alexa Fluor® 594 WGA was used to label plasma membranes (red) at a 1/200 dilution for 1h. DAPI was used to stain the cell nuclei (blue) at a concentration of 1.43µM.
This product has been referenced in:
See all 9 publications for this product
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All lanes : Anti-SREBP2 antibody (ab30682) at 2.5 µg/ml
Lane 1 : Human fibroblast cell lysate
Lane 2 : Rat brown fat homogenate
Lane 3 : Rat testis supernatant
Lysates/proteins at 60 µg per lane.
Predicted band size : 126 kDa
Observed bands 126 kDa, 55kDa (cleaved form)

ICC/IF image of ab30682 stained HeLa cells. The cells were 4% PFA fixed (10 min) and then incubated in 1%BSA / 10% normal goat serum / 0.3M glycine in 0.1% PBS-Tween for 1h to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody (ab30682, 1µg/ml) overnight at +4°C. The secondary antibody (green) was Alexa Fluor® 488 goat anti-rabbit IgG (H+L) used at a 1/1000 dilution for 1h. Alexa Fluor® 594 WGA was used to label plasma membranes (red) at a 1/200 dilution for 1h. DAPI was used to stain the cell nuclei (blue) at a concentration of 1.43µM.
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