Anti-Acid sphingomyelinase antibody [OTI3H7] - BSA and Azide free (ab273656)
Key features and details
- Mouse monoclonal [OTI3H7] to Acid sphingomyelinase - BSA and Azide free
- Suitable for: WB, IHC-P
- Reacts with: Human
- Isotype: IgG1
Overview
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Product name
Anti-Acid sphingomyelinase antibody [OTI3H7] - BSA and Azide free
See all Acid sphingomyelinase primary antibodies -
Description
Mouse monoclonal [OTI3H7] to Acid sphingomyelinase - BSA and Azide free -
Host species
Mouse -
Tested Applications & Species
See all applications and species dataApplication Species IHC-P HumanWB Human -
Immunogen
Recombinant fragment corresponding to Human Acid sphingomyelinase aa 50-350. NP_000534 Produced in E.coli.
Database link: P17405 -
Positive control
- IHC-P: Human breast adenocarcinoma, lymphoma, colon adenocarcinoma, lung carcinoma, endometrium adenocarcinoma, liver carcinoma, thyroid carcinoma, prostate carcinoma, ovary adenocarcinoma, kidney carcinoma, pancreas, ovary, lymph node, lung, colon, endometrium, liver, prostate, bladder, kidney and tonsil tissue. WB: pCMV6-ENTRY Acid sphingomyelinase cDNA transfected HEK-293T cell lysate.
Properties
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Form
Liquid -
Storage instructions
Shipped at 4°C. Store at +4°C short term (1-2 weeks). Upon delivery aliquot. Store at -20°C long term. Avoid freeze / thaw cycle. -
Storage buffer
pH: 7.3
Constituent: PBS -
Carrier free
Yes -
Concentration information loading...
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Purity
Protein A/G purified -
Purification notes
Purified from TCS. -
Clonality
Monoclonal -
Clone number
OTI3H7 -
Isotype
IgG1 -
Research areas
Images
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Paraffin-embedded human tonsil tissue stained for Acid sphingomyelinase using ab273656 at 1/150 dilution.
Heat-induced epitope retrieval was performed using 1 mM EDTA in 10 mM Tris, pH 8.5, 120°C for 3 mins.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, pH 7.3, 8% trehalose.
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All lanes : Same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide at 1/2000 dilution
Lane 1 : pCMV6-ENTRY control cDNA transfected HEK-293T cell lysate
Lane 2 : pCMV6-ENTRY Acid sphingomyelinase cDNA transfected HEK-293T cell lysate
Lysates/proteins at 5 µg per lane.
Predicted band size: 70 kDaCells were transfected with cDNA for 48 hrs and lysed.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, pH 7.3, 8% trehalose.
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Paraffin-embedded human thyroid carcinoma tissue stained for Acid sphingomyelinase using ab273656 at 1/150 dilution.
Heat-induced epitope retrieval was performed using 1 mM EDTA in 10 mM Tris, pH 8.5, 120°C for 3 mins.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, pH 7.3, 8% trehalose.
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Paraffin-embedded human prostate tissue stained for Acid sphingomyelinase using ab273656 at 1/150 dilution.
Heat-induced epitope retrieval was performed using 1 mM EDTA in 10 mM Tris, pH 8.5, 120°C for 3 mins.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, pH 7.3, 8% trehalose.
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Paraffin-embedded human prostate carcinoma tissue stained for Acid sphingomyelinase using ab273656 at 1/150 dilution.
Heat-induced epitope retrieval was performed using 1 mM EDTA in 10 mM Tris, pH 8.5, 120°C for 3 mins.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, pH 7.3, 8% trehalose.
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Paraffin-embedded human pancreas tissue stained for Acid sphingomyelinase using ab273656 at 1/150 dilution.
Heat-induced epitope retrieval was performed using 1 mM EDTA in 10 mM Tris, pH 8.5, 120°C for 3 mins.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, pH 7.3, 8% trehalose.
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Paraffin-embedded human ovary tissue stained for Acid sphingomyelinase using ab273656 at 1/150 dilution.
Heat-induced epitope retrieval was performed using 1 mM EDTA in 10 mM Tris, pH 8.5, 120°C for 3 mins.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, pH 7.3, 8% trehalose.
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Paraffin-embedded human ovary adenocarcinoma tissue stained for Acid sphingomyelinase using ab273656 at 1/150 dilution.
Heat-induced epitope retrieval was performed using 1 mM EDTA in 10 mM Tris, pH 8.5, 120°C for 3 mins.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, pH 7.3, 8% trehalose.
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Paraffin-embedded human lymphoma tissue stained for Acid sphingomyelinase using ab273656 at 1/150 dilution.
Heat-induced epitope retrieval was performed using 1 mM EDTA in 10 mM Tris, pH 8.5, 120°C for 3 mins.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, pH 7.3, 8% trehalose.
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Paraffin-embedded human lymph node tissue stained for Acid sphingomyelinase using ab273656 at 1/150 dilution.
Heat-induced epitope retrieval was performed using 1 mM EDTA in 10 mM Tris, pH 8.5, 120°C for 3 mins.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, pH 7.3, 8% trehalose.
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Paraffin-embedded human lung tissue stained for Acid sphingomyelinase using ab273656 at 1/150 dilution.
Heat-induced epitope retrieval was performed using 1 mM EDTA in 10 mM Tris, pH 8.5, 120°C for 3 mins.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, pH 7.3, 8% trehalose.
-
Paraffin-embedded human lung carcinoma tissue stained for Acid sphingomyelinase using ab273656 at 1/150 dilution.
Heat-induced epitope retrieval was performed using 1 mM EDTA in 10 mM Tris, pH 8.5, 120°C for 3 mins.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, pH 7.3, 8% trehalose.
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Paraffin-embedded human liver tissue stained for Acid sphingomyelinase using ab273656 at 1/150 dilution.
Heat-induced epitope retrieval was performed using 1 mM EDTA in 10 mM Tris, pH 8.5, 120°C for 3 mins.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, pH 7.3, 8% trehalose.
-
Paraffin-embedded human liver carcinoma tissue stained for Acid sphingomyelinase using ab273656 at 1/150 dilution.
Heat-induced epitope retrieval was performed using 1 mM EDTA in 10 mM Tris, pH 8.5, 120°C for 3 mins.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, pH 7.3, 8% trehalose.
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Paraffin-embedded human kidney tissue stained for Acid sphingomyelinase using ab273656 at 1/150 dilution.
Heat-induced epitope retrieval was performed using 1 mM EDTA in 10 mM Tris, pH 8.5, 120°C for 3 mins.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, pH 7.3, 8% trehalose.
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Paraffin-embedded human kidney carcinoma tissue stained for Acid sphingomyelinase aab273656 at 1/150 diution.
Heat-induced epitope retrieval was performed using 1 mM EDTA in 10 mM Tris, pH 8.5, 120°C for 3 mins.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, pH 7.3, 8% trehalose.
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Paraffin-embedded human endometrium tissue stained for Acid sphingomyelinase using ab273656 at 1/150 dilution.
Heat-induced epitope retrieval was performed using 1 mM EDTA in 10 mM Tris, pH 8.5, 120°C for 3 mins.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, pH 7.3, 8% trehalose.
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Paraffin-embedded human endometrium adenocarcinoma tissue stained for Acid sphingomyelinase using ab273656 at 1/150 dilution.
Heat-induced epitope retrieval was performed using 1 mM EDTA in 10 mM Tris, pH 8.5, 120°C for 3 mins.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, pH 7.3, 8% trehalose.
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Paraffin-embedded human colon tissue stained for Acid sphingomyelinase using ab273656 at 1/150 dilution.
Heat-induced epitope retrieval was performed using 1 mM EDTA in 10 mM Tris, pH 8.5, 120°C for 3 mins.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, pH 7.3, 8% trehalose.
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Paraffin-embedded human colon adenocarcinoma tissue stained for Acid sphingomyelinase using ab273656 at 1/150 dilution.
Heat-induced epitope retrieval was performed using 1 mM EDTA in 10 mM Tris, pH 8.5, 120°C for 3 mins.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, pH 7.3, 8% trehalose.
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Paraffin-embedded human breast adenocarcinoma tissue stained for Acid sphingomyelinase using ab273656 at 1/150 dilution.
Heat-induced epitope retrieval was performed using 1 mM EDTA in 10 mM Tris, pH 8.5, 120°C for 3 mins.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, pH 7.3, 8% trehalose.
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Paraffin-embedded human bladder tissue stained for Acid sphingomyelinase using ab273656 at 1/150 dilution.
Heat-induced epitope retrieval was performed using 1 mM EDTA in 10 mM Tris, pH 8.5, 120°C for 3 mins.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, pH 7.3, 8% trehalose.