Rabbit Polyclonal SHMT2/SHMT antibody. C-terminal. Suitable for WB, IHC-P, ICC/IF and reacts with Mouse, Human, Rat samples. Cited in 10 publications. Immunogen corresponding to Recombinant Fragment Protein within Human Serine hydroxymethyltransferase, mitochondrial aa 250 to C-terminus.
View Alternative Names
SHMT, Glycine hydroxymethyltransferase, Serine methylase, SHMT2
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-SHMT2/SHMT antibody - C-terminal (AB180786)
Immunofluorescence staining of U-2 OS cells stained for SHMT2/SHMT with ab180786 at 1/100 dilution. Nuclei are labeled with DAPI (Blue).
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-SHMT2/SHMT antibody - C-terminal (AB180786)
Paraffin-embedded human liver cancer tissue stained for SHMT2/SHMT using ab180786 at 1/100 dilution in immunohistochemical analysis.
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-SHMT2/SHMT antibody - C-terminal (AB180786)
Immunofluorescence staining of L929 cells stained for SHMT2/SHMT with ab180786 at 1/100 dilution. Nuclei are labeled with DAPI (Blue).
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-SHMT2/SHMT antibody - C-terminal (AB180786)
Paraffin-embedded rat spleen tissue stained for SHMT2/SHMT using ab180786 at 1/100 dilution in immunohistochemical analysis.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-SHMT2/SHMT antibody - C-terminal (AB180786)
Paraffin-embedded mouse spleen tissue stained for SHMT2/SHMT using ab180786 at 1/100 dilution in immunohistochemical analysis.
- WB
Supplier Data
Western blot - Anti-SHMT2/SHMT antibody - C-terminal (AB180786)
Blocking buffer : 3% nonfat dry milk in TBST.
All lanes:
Western blot - Anti-SHMT2/SHMT antibody - C-terminal (ab180786) at 1/1000 dilution
Lane 1:
HeLa cell lysate at 25 µg
Lane 2:
OVCAR3 cell lysate at 25 µg
Lane 3:
22Rv1 cell lysate at 25 µg
Lane 4:
Mouse liver tissue lysate at 25 µg
Lane 5:
Mouse kidney tissue lysate at 25 µg
Secondary
All lanes:
HRP Goat Anti-Rabbit IgG (H+L)
Predicted band size: 56 kDa
true
- WB
Lab
Western blot - Anti-SHMT2/SHMT antibody - C-terminal (AB180786)
Western blot : Rabbit Polyclonal to SHMT2/SHMT ab180786 staining at 1/1000 dilution, shown in green; Mouse anti GAPDH (ab8245) loading control staining at 1/20,000 dilution, shown in magenta. A band was observed at 55 kDa in Wild-type A549 cell lysates with no signal observed at this size in SHMT2 knockout A549 cell line. To generate this image, samples were run on an SDS-PAGE gel then transferred onto a nitrocellulose membrane. Membranes were blocked in 3pc 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-Rabbit 800CW & Goat anti-Mouse 680RD at 1/20,000 dilution.
All lanes:
Western blot - Anti-SHMT2/SHMT antibody - C-terminal (ab180786) at 1/1000 dilution
Lane 1:
Wild-type A549 at 20 µg
Lane 2:
Western blot - Human SHMT2 knockout A549 cell line (<a href='/en-us/products/cell-lines/human-shmt2-knockout-a549-cell-line-ab301223'>ab301223</a>) at 20 µg
Lane 3:
HeLa
Secondary
Lanes 1 - 3:
Goat anti-Rabbit 800CW at 1/20000 dilution
Lanes 1 - 3:
Goat anti-Mouse 680RD at 1/20000 dilution
Predicted band size: 56 kDa
Observed band size: 55 kDa,37 kDa
false
Reactivity data
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
The enzyme facilitates essential reactions in mitochondrial nucleotide synthesis. SHMT2 operates within a tetrameric complex that provides one-carbon units for cellular biosynthetic processes. The activity of SHMT2 links mitochondrial serine utilization directly to the folate cycle which is essential for the synthesis of purines and thymidylate. The efficient production of these nucleotides is important for rapidly dividing cells supporting their proliferation and maintenance.
Pathways
SHMT2 takes part in the folate and methionine metabolism pathways. It interacts with proteins like methylenetetrahydrofolate dehydrogenase and thymidylate synthase which are essential for one-carbon metabolism. These interactions integrate SHMT2 activity into a larger network that balances the supply of nucleotides according to the cellular demand impacting vital pathways like DNA replication and repair.
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Target data
Publications (10)
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Science advances 11:eadq1575 PubMed40184463
2025
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Cell death & disease 14:525 PubMed37582769
2023
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Unspecified reactive species
Cancer cell international 20:587 PubMed33372599
2020
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Cancer management and research 12:11169-11181 PubMed33173349
2020
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Unspecified reactive species
Nan fang yi ke da xue xue bao = Journal of Southern Medical University 40:506-512 PubMed32895129
2020
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Unspecified reactive species
Cancers 12: PubMed32106628
2020
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Nature genetics 51:990-998 PubMed31133746
2019
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American journal of cancer research 9:250-269 PubMed30906627
2019
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Unspecified reactive species
OncoTargets and therapy 10:3781-3788 PubMed28794642
2017
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Unspecified application
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Unspecified reactive species
OncoTargets and therapy 8:1069-74 PubMed25999742
2015
Applications
IHC-P
Species
Human
Product promise
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