- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-TMUB1 antibody [EPR14066] (AB180586)
Immunofluorescent analysis of 4% paraformaldehyde fixed HepG2 cells labeling TMUB1 with ab180586 at 1/500 (green). Dapi staining shown in blue.
- Flow Cyt (Intra)
Supplier Data
Flow Cytometry (Intracellular) - Anti-TMUB1 antibody [EPR14066] (AB180586)
Intracellular flow cytometric analysis of 2% paraformaldehyde fixedHeLa cells labeling TMUB1 with ab180586 at 1/70 (pink). Control shown in green.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-TMUB1 antibody [EPR14066] (AB180586)
Immunohistochemical analysis of paraffin embedded Human liver tissue labeling TMUB1 with ab180586 at 1/100.
Perform heat mediated antigen retrieval with EDTA buffer pH 9 before commencing with IHC staining protocol.
- WB
Lab
Western blot - Anti-TMUB1 antibody [EPR14066] (AB180586)
Lanes 1- 3 : Merged signal (red and green). Green - ab180586 observed at 27 kDa. Red - Anti-GAPDH antibody [6C5] - Loading Control (ab8245) observed at 37 kDa.
ab180586 was shown to react with TMUB1 in wild-type HeLa (Human epithelial line from cervix adenocarcinoma) cells in western blot. Loss of signal was observed when knockout cell line ab265852 (knockout cell lysate ab258237) was used. Wild-type HeLa (Human epithelial cell line from cervix adenocarcinoma) and TMUB1 knockout HeLa (Human epithelial cell line from cervix adenocarcinoma) cell lysates were subjected to SDS-PAGE. Membrane was blocked for 1 hour at room temperature in 0.1% TBST with 3% non-fat dried milk. ab180586 and Anti-GAPDH antibody [6C5] - Loading Control (ab8245) overnight at 4°C at a 1 in 10000 dilution and a 1 in 20000 dilution respectively. Blots were developed with Goat anti-Rabbit IgG H&L (IRDye®800CW) preadsorbed (ab216773) and Goat anti-Mouse IgG H&L (IRDye®680RD) preadsorbed (ab216776) secondary antibodies at 1 in 20000 dilution for 1 hour at room temperature before imaging.
All lanes:
Western blot - Anti-TMUB1 antibody [EPR14066] (ab180586) at 1/10000 dilution
Lane 1:
Wild-type HeLa (Human epithelial cell line from cervix adenocarcinoma) cell lysate at 20 µg
Lane 2:
Western blot - Human TMUB1 knockout HeLa cell lysate (<a href='/ko/products/cell-lysates/human-tmub1-knockout-hela-cell-lysate-ab258237'>ab258237</a>) at 20 µg
Lane 3:
HepG2 (Human liver hepatocellular carcinoma cell line) cell lysate cell lysate at 20 µg
Predicted band size: 26 kDa
Observed band size: 27 kDa
false
- WB
Lab
Western blot - Anti-TMUB1 antibody [EPR14066] (AB180586)
Lanes 1 - 4 : Merged signal (red and green). Green - ab180586 observed at 27 kDa. Red - loading control ab8245 (Mouse anti-GAPDH antibody [6C5]) observed at 37 kDa.
ab180586 was shown to react with TMUB1 in wild-type HeLa cells in Western blot with loss of signal observed in TMUB1 knockout cell line ab278130 (knockout cell lysate ab278185). Wild-type HeLa and tmub1 knockout cell lysates were subjected to SDS-PAGE. Membranes were blocked in fluorescent western blot (TBS-based) blocking solution before incubation with ab180586 and ab8245 (Mouse anti-GAPDH antibody [6C5]) overnight at 4 °C at a 1 in 10000 dilution and a 1 in 20000 dilution respectively. Blots were incubated with Goat anti-Rabbit IgG H&L (IRDye® 800CW) preabsorbed (ab216773) and Goat anti-Mouse IgG H&L (IRDye® 680RD) preabsorbed (ab216776) secondary antibodies at 1 in 20000 dilution for 1 h at room temperature before imaging.
All lanes:
Western blot - Anti-TMUB1 antibody [EPR14066] (ab180586) at 1/10000 dilution
Lane 1:
Wild-type HeLa cell lysate at 20 µg
Lane 2:
TMUB1 knockout HeLa cell lysate at 20 µg
Lane 2:
Western blot - Human TMUB1 knockout HeLa cell line (<a href='/ko/products/cell-lines/human-tmub1-knockout-hela-cell-line-ab278130'>ab278130</a>)
Lane 3:
HepG2 cell lysate at 20 µg
Lane 4:
Human Cerebellum tissue lysate at 20 µg
Predicted band size: 26 kDa
Observed band size: 27 kDa
false
- WB
Supplier Data
Western blot - Anti-TMUB1 antibody [EPR14066] (AB180586)
All lanes:
Western blot - Anti-TMUB1 antibody [EPR14066] (ab180586) at 1/50000 dilution
Lane 1:
Human fetal liver tissue lysate at 20 µg
Lane 2:
Human cerebellum tissue lysate at 20 µg
Lane 3:
HepG2 cell line lysate lysate at 20 µg
Lane 4:
HeLa cell line lysate at 10 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated at 1/1000 dilution
Predicted band size: 26 kDa
Observed band size: 24 kDa,27 kDa
false
관련 conjugated 항체와 다양한 조성의 항체 (1)
-
Anti-TMUB1 antibody [EPR14066] - BSA and Azide free
Reactivity 정보
제품 세부 정보
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.
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대체 명칭 보기
제품이 사용된 논문 (3)
Recent publications for all applications. Explore the 전체 목록 and refine your search
Life science alliance 7: PubMed38782601
2024
Applications
Unspecified application
Species
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Molecular cell 79:768-781.e7 PubMed32738194
2020
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Unspecified application
Species
Unspecified reactive species
Molecular medicine reports 17:4337-4344 PubMed29344642
2018
Applications
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Species
Unspecified reactive species
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Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
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