Anti-LLGL1 + LLGL2 antibody [EPR18899]
- RabMAb
- Recombinant
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(3 Publications)
Rabbit Recombinant Monoclonal LLGL1 antibody. Suitable for IHC-P, ICC/IF, IP, WB and reacts with Human samples. Cited in 3 publications.
View Alternative Names
DLG4, HUGL, HUGL1, LLGL1, Lethal(2) giant larvae protein homolog 1, LLGL, Hugl-1, Human homolog to the D-lgl gene protein, LLGL scribble cell polarity complex component 2, HGL, Lethal(2) giant larvae protein homolog 2, LLGL2
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-LLGL1 + LLGL2 antibody [EPR18899] (AB183021)
Immunohistochemical analysis of paraffin-embedded Human kidney tissue labeling LLGL1 with ab183021 at 1/100 dilution followed by Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/500 dilution. Cytoplasm staining on Human kidney is observed. Counter stained with Hematoxylin.
Secondary antibody only control : Used PBS instead of primary antibody secondary antibody is Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/500 dilution.
Perform heat mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-LLGL1 + LLGL2 antibody [EPR18899] (AB183021)
Immunohistochemical analysis of paraffin-embedded Human stomach tissue labeling LLGL1 with ab183021 at 1/100 dilution followed by Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/500 dilution. Cytoplasm staining on Human stomach is observed. Counter stained with Hematoxylin.
Secondary antibody only control : Used PBS instead of primary antibody secondary antibody is Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/500 dilution.
Perform heat mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-LLGL1 + LLGL2 antibody [EPR18899] (AB183021)
Immunofluorescent analysis of 4% paraformaldehyde-fixed 0.1% Triton X-100 permeabilized SW480 (Human colorectal adenocarcinoma cell line) cells labeling LLGL1 with ab183021 at 1/100 dilution followed by Goat anti-rabbit IgG (Alexa Fluor® 488) (ab150077) secondary antibody at 1/1000 dilution (green). Confocal image showing cytoplasmic staining on SW480 cell line. The nuclear counter stain is DAPI (blue). Tubulin is detected with Anti-alpha Tubulin antibody [EPR18899]-Loading Control (ab7291) at 1/1000 dilution and Goat Anti-Mouse IgG (AlexaFluor®594) preadsorbed (ab150120) at 1/1000 dilution (red).
The negative controls are as follows :
-ve control 1 : ab183021 at 1/100 dilution followed by ab150120 at 1/1000 dilution.
-ve control 2 : ab7291 at 1/1000 dilution followed by ab150077 at 1/1000 dilution.
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-LLGL1 + LLGL2 antibody [EPR18899] (AB183021)
Immunofluorescent analysis of 4% paraformaldehyde-fixed 0.1% Triton X-100 permeabilized HepG2 (Human liver hepatocellular carcinoma cell line) cells labeling LLGL1 with ab183021 at 1/100 dilution followed by Goat anti-rabbit IgG (Alexa Fluor® 488) (ab150077) secondary antibody at 1/1000 dilution (green). Confocal image showing cytoplasmic staining on HepG2 cell line. The nuclear counter stain is DAPI (blue). Tubulin is detected with Anti-alpha Tubulin antibody [EPR18899]-Loading Control (ab7291) at 1/1000 dilution and Goat Anti-Mouse IgG (AlexaFluor®594) preadsorbed (ab150120) at 1/1000 dilution (red).
The negative controls are as follows :
-ve control 1 : ab183021 at 1/100 dilution followed by ab150120 at 1/1000 dilution.
-ve control 2 : ab7291 at 1/1000 dilution followed by ab150077 at 1/1000 dilution.
- IP
Supplier Data
Immunoprecipitation - Anti-LLGL1 + LLGL2 antibody [EPR18899] (AB183021)
LLGL1was immunoprecipitated from 1mg of HepG2 (Human liver hepatocellular carcinoma cell line) whole cell lysate with ab183021 at 1/50 dilution. Western blot was performed from the immunoprecipitate using ab183021 at 1/1000 dilution. VeriBlot for IP Detection Reagent (HRP) (ab131366), was used for detection at 1/10000 dilution.
Lane 1 : HepG2 whole cell lysate 10μg (Input).
Lane 2 : ab183021 IP in HepG2 whole cell lysate.
Lane 3 : Rabbit IgG, monoclonal [EPR18899] - Isotype Control (ab172730) instead of ab183021 in HepG2 whole cell lysate.
Blocking and dilution buffer and concentration : 5% NFDM/TBST.
Exposure time : 10 seconds.
All lanes:
Immunoprecipitation - Anti-LLGL1 + LLGL2 antibody [EPR18899] (ab183021)
Predicted band size: 113 kDa
false
- WB
Lab
Western blot - Anti-LLGL1 + LLGL2 antibody [EPR18899] (AB183021)
Blocking buffer : 5% NFDM/TBST
Dilution buffer : 5% NFDM/TBST
All lanes:
Western blot - Anti-LLGL1 + LLGL2 antibody [EPR18899] (ab183021) at 1/5000 dilution
Lane 1:
HepG2 cell lysate at 10 µg
Lane 2:
A431 cell lysate at 10 µg
Lane 3:
SW480 cell lysate at 10 µg
Lane 4:
A459 cell lysate at 10 µg
Lane 5:
Caco-2 cell lysate at 10 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
Predicted band size: 113 kDa
Observed band size: 115 kDa
false
- WB
Supplier Data
Western blot - Anti-LLGL1 + LLGL2 antibody [EPR18899] (AB183021)
Blocking buffer : 5% NFDM/TBST.
We recommend to use 1% SDS Hot lysis method to get desired WB results.
All lanes:
Western blot - Anti-LLGL1 + LLGL2 antibody [EPR18899] (ab183021) at 1/2000 dilution
Lane 1:
A431 (Human epidermoid carcinoma epithelial cell) whole cell lysate prepared in RIPA lysis method at 15 µg
Lane 2:
A431 (Human epidermoid carcinoma epithelial cell) whole cell lysate prepared in 1% SDS Hot lysis method at 15 µg
Lane 3:
SW480 (Human colorectal adenocarcinoma epithelial cell) whole cell lysate prepared in RIPA lysis method at 15 µg
Lane 4:
SW480 (Human colorectal adenocarcinoma epithelial cell) whole cell lysate prepared in 1% SDS Hot lysis method at 15 µg
Lane 5:
Caco-2 (Human colorectal adenocarcinoma epithelial cell) whole cell lysate prepared in RIPA lysis method at 15 µg
Lane 6:
Caco-2 (Human colorectal adenocarcinoma epithelial cell) whole cell lysate prepared in 1% SDS Hot lysis method at 15 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/20000 dilution
Predicted band size: 113 kDa
Observed band size: 115 kDa
false
Exposure time: 20s
- WB
Supplier Data
Western blot - Anti-LLGL1 + LLGL2 antibody [EPR18899] (AB183021)
Blocking/dilution buffer : 5% NFDM/TBST.
Exposure time Lane 1/2 : 3 minutes; Lane 3 : 15 seconds.
All lanes:
Western blot - Anti-LLGL1 + LLGL2 antibody [EPR18899] (ab183021) at 1/2000 dilution
Lane 1:
Human fetal liver lysate at 10 µg
Lane 2:
Human fetal heart lysate at 10 µg
Lane 3:
Human fetal kidney lysate at 10 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG Peroxidase Conjugate, specific to the non-reduced form of IgG at 1/10000 dilution
Predicted band size: 113 kDa
Observed band size: 115 kDa
false
- WB
Supplier Data
Western blot - Anti-LLGL1 + LLGL2 antibody [EPR18899] (AB183021)
Blocking buffer : 5% NFDM/TBST.
All lanes:
Western blot - Anti-LLGL1 + LLGL2 antibody [EPR18899] (ab183021) at 1/10000 dilution
Lane 1:
His tagged human LLGL1 full length recombinant protein at 0.01 µg
Lane 2:
Flag tagged human LLGL2 full length recombinant protein at 0.01 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/20000 dilution
Predicted band size: 113 kDa
Observed band size: 120 kDa
false
Exposure time: 40s
Related conjugates and formulations (1)
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Anti-LLGL1 + LLGL2 antibody [EPR18899] - BSA and Azide free
Reactivity data
Product details
Patented technology
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
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.
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
In epithelial cells and neural progenitors LLGL1 and LLGL2 are essential for maintaining cell polarity contributing to the structural stability and function of tissues. Both proteins are part of the Scribble complex a multi-protein assembly that regulates cell polarity and adhesion. By ensuring proper orientation and polarization of cells they are involved in tissue homeostasis and developmental processes.
Pathways
Cell polarity and division control involves the LLGL1 and LLGL2 proteins. They are key components of the PAR (Partitioning-defective) pathway interplaying with proteins like aPKC and PAR-6 essential for spatial cellular orientation. Additionally they play a role in the Hippo signaling pathway which is important for organ size regulation and cell proliferation working alongside proteins such as YAP/TAZ.
Product protocols
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Target data
Additional targets
Publications (3)
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Theranostics 15:9580-9600 PubMed41041054
2025
Applications
Unspecified application
Species
Unspecified reactive species
Molecular therapy. Nucleic acids 35:102363 PubMed39558906
2024
Applications
Unspecified application
Species
Unspecified reactive species
The Journal of biological chemistry 297:101354 PubMed34717957
2021
Applications
Unspecified application
Species
Unspecified reactive species
Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
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