Anti-Scavenging Receptor SR-BI antibody [25/CLA-1]
- BOND RX™ Validated
- Recombinant
- KO Validated
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Mouse Recombinant Monoclonal Scavenging Receptor SR-BI antibody. Suitable for IHC-P, WB and reacts with Human samples.
View Alternative Names
CD36, CD36L1, CLA1, SCARB1, Scavenger receptor class B member 1, SRB1, CD36 and LIMPII analogous 1, CD36 antigen-like 1, SR-BI, CLA-1
- IHC
Supplier Data
Immunohistochemistry - Anti-Scavenging Receptor SR-BI antibody [25/CLA-1] (AB300632)
Immunohistochemical analysis of paraffin-embedded Human hepatocellular tissue labeling Scavenging Receptor SR-BI with ab300632 at 1/1000 (1.01 µg/mL) followed by a LeicaDS9800 (Bond Polymer Refine Detection) was used at Ready to use dilution. Positive staining on human hepatocellular carcinoma. The section was incubated with abxxxxxx for 30mins at room temperature, followed by anti-mouse IgG1 antibody (ab125913) for 8 mins during the LeicaDS9800 kit staining procedure.The immunostaining was performed on a Leica Biosystems BOND® RX instrument Counterstained with Hematoxylin. Secondary antibody only control : Secondary antibody is LeicaDS9800 (Bond Polymer Refine Detection) was used at Ready to use dilution. Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins
- IHC
Supplier Data
Immunohistochemistry - Anti-Scavenging Receptor SR-BI antibody [25/CLA-1] (AB300632)
Immunohistochemical analysis of paraffin-embedded Human cerebrum tissue labeling Scavenging Receptor SR-BI with ab300632 at 1/1000 (1.01 µg/mL) followed by a LeicaDS9800 (Bond Polymer Refine Detection) was used at Ready to use dilution. Positive staining on blood vessels of human cerebrum. The section was incubated with abxxxxxx for 30mins at room temperature, followed by anti-mouse IgG1 antibody (ab125913) for 8 mins during the LeicaDS9800 kit staining procedure.The immunostaining was performed on a Leica Biosystems BOND® RX instrument Counterstained with Hematoxylin. Secondary antibody only control : Secondary antibody is LeicaDS9800 (Bond Polymer Refine Detection) was used at Ready to use dilution. Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins
- IHC
Supplier Data
Immunohistochemistry - Anti-Scavenging Receptor SR-BI antibody [25/CLA-1] (AB300632)
Immunohistochemical analysis of paraffin-embedded Human liver tissue labeling Scavenging Receptor SR-BI with ab300632 at 1/1000 (1.01 µg/mL) followed by a LeicaDS9800 (Bond Polymer Refine Detection) was used at Ready to use dilution. Positive staining on human liver. The section was incubated with abxxxxxx for 30mins at room temperature, followed by anti-mouse IgG1 antibody (ab125913) for 8 mins during the LeicaDS9800 kit staining procedure.The immunostaining was performed on a Leica Biosystems BOND® RX instrument Counterstained with Hematoxylin. Secondary antibody only control : Secondary antibody is LeicaDS9800 (Bond Polymer Refine Detection) was used at Ready to use dilution. Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins
- WB
Lab
Western blot - Anti-Scavenging Receptor SR-BI antibody [25/CLA-1] (AB300632)
False colour image of Western blot : Anti-Scavenging Receptor SR-BI antibody [25/CLA-1] staining at 1/1000 dilution, shown in green; Rabbit Anti-GAPDH antibody [EPR16891] (ab181602) loading control staining at 1/20000 dilution, shown in red. In Western blot, ab300632 was shown to bind specifically to Scavenging Receptor SR-BI. A band was observed at 70 and 75 kDa in wild-type HEK-293T cell lysates with no signal observed at this size in SCARB1 knockout cell line ab282646. To generate this image, wild-type and SCARB1 knockout HEK-293T cell lysates were analysed. First, samples were run on an SDS-PAGE gel then transferred onto a nitrocellulose membrane. Membranes were blocked in 3 % milk in TBS-0.1 % Tween® 20 (TBS-T) before incubation with primary antibodies overnight at 4 °C. Blots were washed four times in TBS-T, incubated with secondary antibodies for 1 h at room temperature, washed again four times then imaged. Secondary antibodies used were Goat anti-Mouse IgG H&L (IRDye® 800CW) preabsorbed (ab216772) and Goat anti-Rabbit IgG H&L (IRDye® 680RD) preabsorbed (ab216777) at 1/20000 dilution.
All lanes:
Western blot - Anti-Scavenging Receptor SR-BI antibody [25/CLA-1] (ab300632) at 1/1000 dilution
Lane 1:
Wild-type HEK-293T cell lysate at 20 µg
Lane 2:
Western blot - Human SCARB1 knockout HEK-293T cell lysate (<a href='/en-us/products/cell-lysates/human-scarb1-knockout-hek-293t-cell-lysate-ab283046'>ab283046</a>)
Lane 2:
Western blot - Human SCARB1 knockout HEK-293T cell line (<a href='/en-us/products/cell-lines/human-scarb1-knockout-hek-293t-cell-line-ab282646'>ab282646</a>)
Lane 2:
SCARB1 knockout HEK-293T cell lysate at 20 µg
Lane 3:
Human Liver cell lysate at 20 µg
Secondary
Lanes 1 - 3:
Western blot - Goat Anti-Rabbit IgG H&L (IRDye® 680RD) preadsorbed (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-irdye-680rd-preadsorbed-ab216777'>ab216777</a>) at 1/20000 dilution
Lanes 1 - 3:
Western blot - Goat anti-Mouse IgG H&L (IRDye® 800CW) preadsorbed (<a href='/en-us/products/secondary-antibodies/goat-mouse-igg-h-l-irdye-800cw-preadsorbed-ab216772'>ab216772</a>) at 1/20000 dilution
Predicted band size: 60 kDa
Observed band size: 70 kDa,75 kDa
false
- WB
Supplier Data
Western blot - Anti-Scavenging Receptor SR-BI antibody [25/CLA-1] (AB300632)
All lanes:
Western blot - Anti-Scavenging Receptor SR-BI antibody [25/CLA-1] (ab300632) at 1/1000 dilution
Lane 1:
LNCaP (human prostate carcinoma epithelial cell), whole cell lysate at 10 µg
Lane 2:
PC-3 (human prostate adenocarcinoma epithelial cell), whole cell lysate at 10 µg
Lane 3:
Human liver tissue lysate at 10 µg
Secondary
All lanes:
Peroxidase-Conjugated Goat anti-Mouse IgG (H+L) at 1/10000 dilution
false
- WB
Supplier Data
Western blot - Anti-Scavenging Receptor SR-BI antibody [25/CLA-1] (AB300632)
All lanes:
Western blot - Anti-Scavenging Receptor SR-BI antibody [25/CLA-1] (ab300632) at 1/1000 dilution
Lane 1:
Wild type HAP1, whole cell lysate at 20 µg
Lane 2:
SCARB1 knockout HAP1, whole cell lysate at 20 µg
Lane 3:
HepG2 (human hepatocellar carcinoma epithelial cell), whole cell lysate 20 at 20 µg
Lane 4:
HeLa (human cervix adenocarcinoma epithelial cell), whole cell lysate at 20 µg
Secondary
Lanes 1 - 4:
Western blot - Goat anti-Mouse IgG H&L (IRDye® 800CW) preadsorbed (<a href='/en-us/products/secondary-antibodies/goat-mouse-igg-h-l-irdye-800cw-preadsorbed-ab216772'>ab216772</a>) at 1/10000 dilution
Lanes 1 - 4:
Western blot - Goat Anti-Rabbit IgG H&L (IRDye® 680RD) preadsorbed (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-irdye-680rd-preadsorbed-ab216777'>ab216777</a>) at 1/10000 dilution
false
Related conjugates and formulations (1)
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Anti-Scavenging Receptor SR-BI antibody [25/CLA-1] (BSA and Azide free)
Reactivity data
Product details
What are the advantages of a recombinant monoclonal antibody?
This product is a recombinant monoclonal antibody, which offers several advantages including:
- - High batch-to-batch consistency and reproducibility
- - Improved sensitivity and specificity
- - Long-term security of supply
- - Animal-free batch production
For more information, read more on recombinant antibodies.
Want a custom formulation?
This antibody clone is manufactured by Abcam. If you require a custom buffer formulation or conjugation for your experiments, please contact orders@abcam.com
Properties and storage information
Form
Purification technique
Storage buffer
Shipped at conditions
Appropriate short-term storage duration
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Aliquoting information
Storage information
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
SR-BI contributes to lipid metabolism by influencing the dynamics of cholesterol and lipid circulation within the body. It forms part of the larger HDL receptor complex which facilitates the selective uptake of lipids without internalizing the entire lipoprotein. Through this mechanism SR-BI assists cells in acquiring necessary components for membrane synthesis and hormone production.
Pathways
SR-BI integrates into the cholesterol biosynthesis pathway and the reverse cholesterol transport pathway. In these pathways SR-BI works closely with proteins like ATP-binding cassette transporter A1 (ABCA1) and lecithin-cholesterol acyltransferase (LCAT). These interactions promote the efflux and transport of cholesterol therefore playing a vital role in lipid regulation and metabolic processes.
Product protocols
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Target data
Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
For licensing inquiries, please contact partnerships@abcam.com