Anti-MBOAT7 antibody [EPR30427-503] - BSA and Azide free
- RabMAb
- Recombinant
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Rabbit Recombinant Monoclonal MBOA7 antibody. Carrier free. Suitable for IHC-P, ICC/IF, WB and reacts with Transfected cell lysate - Human, Human samples.
View Alternative Names
BB1, LENG4, OACT7, Membrane-bound acylglycerophosphatidylinositol O-acyltransferase MBOAT7, 1-acylglycerophosphatidylinositol O-acyltransferase, Bladder and breast carcinoma-overexpressed gene 1 protein, Leukocyte receptor cluster member 4, Lysophosphatidylinositol acyltransferase, Lysophospholipid acyltransferase 7, Membrane-bound O-acyltransferase domain-containing protein 7, LPIAT, Lyso-PI acyltransferase, LPLAT 7, O-acyltransferase domain-containing protein 7, h-mboa-7
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-MBOAT7 antibody [EPR30427-503] - BSA and Azide free (AB325504)
This data was developed using ab325494, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Human bladder cancer tissue labeling LENG4 with ab325494 at 1/500 (1.066 µg/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Cytoplasmic staining on human bladder cancer.
The primary antibody was incubated for 30 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument.
Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-MBOAT7 antibody [EPR30427-503] - BSA and Azide free (AB325504)
This data was developed using ab325494, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Panel A : HEK-293T (human embryonic kidney epithelial cell) transfected with a MBOAT7 expression vector containing a his tag Panel B : HEK-293T (human embryonic kidney epithelial cell) transfected with a SPZ1 expression vector containing a his tag Panel C : HEK-293T (human embryonic kidney epithelial cell) transfected with an empty vector containing a myc-His-tag® tissue labeling LENG4 with ab325494 at 1/500 (1.066 µg/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on (A) HEK-293T transfected with a MBOAT7 expression vector containing a his tag, no staining on (B) HEK-293T transfected with a SPZ1 expression vector containing a his tag and (C) HEK-293T cells transfected with empty vector containing a myc-His-tag.
The primary antibody was incubated for 30 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument.
Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-MBOAT7 antibody [EPR30427-503] - BSA and Azide free (AB325504)
This data was developed using ab325494, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Human testis tissue labeling LENG4 with ab325494 at 1/500 (1.066 µg/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Cytoplasmic staining on human testis.
The primary antibody was incubated for 30 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument.
Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-MBOAT7 antibody [EPR30427-503] - BSA and Azide free (AB325504)
This data was developed using ab325494, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Panel A : NIH : OVCAR-3 (human ovary adenocarcinoma epithelial cell) cell pellet Panel B : PC-3 (human prostate adenocarcinoma epithelial cell) cell pellet Panel C : SW620 (human colorectal adenocarcinoma epithelial cell) cell pellet Panel D : THP-1 (human monocytic leukemia monocyte) cell pellet tissue labeling LENG4 with ab325494 at 1/500 (1.066 µg/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on (A) NIH : OVCAR-3 and (B) PC-3, no staining in (C) SW620 and (D) THP-1.
The primary antibody was incubated for 30 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument.
Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-MBOAT7 antibody [EPR30427-503] - BSA and Azide free (AB325504)
This data was developed using ab325494, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Human breast cancer tissue labeling LENG4 with ab325494 at 1/500 (1.066 µg/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Cytoplasmic staining on human breast cancer.
The primary antibody was incubated for 30 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument.
Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
- ICC/IF
Lab
Immunocytochemistry/ Immunofluorescence - Anti-MBOAT7 antibody [EPR30427-503] - BSA and Azide free (AB325504)
This data was developed using ab325494, the same antibody clone in a different buffer formulation.
Immunofluorescent analysis of 100% methanol-fixed, 0.1% TritonX-100 permeabilized HT-1197(human urinary bladder carcinoma cell);THP-1(human monocytic leukemia monocyte) cells labelling LENG4 with ab325494 at 1/500 (1.066 µg/ml) dilution , followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 dilution (Green).
Confocal image showing cytoplasmic staining in HT-1197 cell line (shown in green). The counterstain was observed in magenta. Nuclear DNA was labelled with DAPI (shown in blue). Low expression : THP-1. Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).
Anti-KDEL mouse monoclonal antibody was used to counterstain tubulin at 1/1000 dilution (Magenta). The Nuclear counterstain was DAPI (Blue).
Secondary antibody only control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 dilution.
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-MBOAT7 antibody [EPR30427-503] - BSA and Azide free (AB325504)
This data was developed using ab325494, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Human liver tissue labeling LENG4 with ab325494 at 1/500 (1.066 µg/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Low expression : Nearly no staining in human liver.
The primary antibody was incubated for 30 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument.
Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-MBOAT7 antibody [EPR30427-503] - BSA and Azide free (AB325504)
This data was developed using ab325494, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Human kidney tissue labeling LENG4 with ab325494 at 1/500 (1.066 µg/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Low expression : Nearly no staining in human kidney.
The primary antibody was incubated for 30 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument.
Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
- WB
Lab
Western blot - Anti-MBOAT7 antibody [EPR30427-503] - BSA and Azide free (AB325504)
This data was developed using ab325494, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
Low expression : lymph node, liver
Samples are non-boiled as boiling may cause protein aggregation.
In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) (1 : 200000) (36KDa).
All lanes:
Western blot - Anti-MBOAT7 antibody [EPR30427-503] (<a href='/en-us/products/primary-antibodies/mboat7-antibody-epr30427-503-ab325494'>ab325494</a>) at 1/1000 dilution
Lane 1:
Human adrenal gland tissue lysate at 20 µg
Lane 2:
Human testis tissue lysate at 20 µg
Lane 3:
Human lymph node tissue lysate at 20 µg
Lane 4:
Human liver tissue lysate at 20 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG (HRP) with minimal cross-reactivity with human IgG at 1/2000 dilution
Observed band size: 40 kDa,36 kDa
false
Exposure time: 180s
- WB
Lab
Western blot - Anti-MBOAT7 antibody [EPR30427-503] - BSA and Azide free (AB325504)
This data was developed using ab325494, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
Low expression : THP-1, SW620
Samples are non-boiled as boiling may cause protein aggregation.
In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) (1 : 200000) (36KDa).
All lanes:
Western blot - Anti-MBOAT7 antibody [EPR30427-503] (<a href='/en-us/products/primary-antibodies/mboat7-antibody-epr30427-503-ab325494'>ab325494</a>) at 1/1000 dilution
Lane 1:
A-172 (human brain glioblastoma cell ) whole cell lysate at 40 µg
Lane 2:
HT-1197 (human urinary bladder carcinoma cell ) whole cell lysate at 40 µg
Lane 3:
NIH:OVCAR-3 (human ovary adenocarcinoma epithelial cell) whole cell lysate at 40 µg
Lane 4:
PC-3 (human prostate adenocarcinoma epithelial cell) whole cell lysate at 40 µg
Lane 5:
THP-1 (human monocytic leukemia monocyte) whole cell lysate at 40 µg
Lane 6:
SW620 (human colorectal adenocarcinoma epithelial cell) whole cell lysate at 40 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
Observed band size: 40 kDa,36 kDa
false
Exposure time: 180s
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.
Conjugation ready
Our carrier-free antibodies are typically supplied in a PBS-only formulation, purified and free of BSA, sodium azide and glycerol. This conjugation-ready format is designed for use with fluorochromes, metal isotopes, oligonucleotides, and enzymes, which makes them ideal for antibody labelling, functional and cell-based assays, flow-based assays (e.g. mass cytometry) and Multiplex Imaging applications.
Use our conjugation kits for antibody conjugates that are ready-to-use in as little as 20 minutes with 1 minute hands-on-time and 100% antibody recovery: available for fluorescent dyes, HRP, biotin and gold.
Compatibility
This product is compatible with the Maxpar® Antibody Labeling Kit from Fluidigm, without the need for antibody preparation. Maxpar® is a trademark of Fluidigm Canada Inc.
Properties and storage information
Form
Purification technique
Storage buffer
Shipped at conditions
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Storage information
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