Rabbit Polyclonal GAPDS antibody. Suitable for WB, IHC-P, ICC/IF and reacts with Mouse, Human samples. Cited in 7 publications. Immunogen corresponding to Recombinant Fragment Protein within Human GAPDHS aa 150-400.
View Alternative Names
GAPD2, GAPDH2, GAPDS, HSD-35, HSD35, GAPDHS, Spermatogenic cell-specific glyceraldehyde 3-phosphate dehydrogenase 2, Spermatogenic glyceraldehyde-3-phosphate dehydrogenase, GAPDH-2
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-GAPDS antibody (AB153802)
Paraffin embedded human gastric cancer tissue stained for GAPDHS using ab153802 at 1/500 dilution in immunohistochemical analysis.
- ICC/IF
Unknown
Immunocytochemistry/ Immunofluorescence - Anti-GAPDS antibody (AB153802)
Immunofluorescent analysis of methanol-fixed MCF7 cells labeling GAPDS with ab153802 at 1/200 dilution. Lower panel co-stained with Hoechst 33342.
- WB
Unknown
Western blot - Anti-GAPDS antibody (AB153802)
10% SDS PAGE
All lanes:
Western blot - Anti-GAPDS antibody (ab153802) at 1/1000 dilution
All lanes:
MCF7 whole cell lysate at 30 µg
Predicted band size: 45 kDa,49 kDa
false
- WB
Supplier Data
Western blot - Anti-GAPDS antibody (AB153802)
10% SDS-PAGE
All lanes:
Western blot - Anti-GAPDS antibody (ab153802) at 1/500 dilution
All lanes:
Mouse testis tissue extract at 50 µg
Predicted band size: 45 kDa
false
- WB
Unknown
Western blot - Anti-GAPDS antibody (AB153802)
10% SDS PAGE
All lanes:
Western blot - Anti-GAPDS antibody (ab153802) at 1/5000 dilution
All lanes:
NIH/3T3 whole cell lysate at 30 µg
Predicted band size: 45 kDa
false
- WB
CiteAb
Western blot - Anti-GAPDS antibody (AB153802)
Western Blotting using Anti-GAPDS antibody, ab153802. Publication image from He, J. et al., 2020, Mol Cancer, 31992303. Legend direct from paper.
circ-MAPK4 behaved as an oncogene in glioma cells. (a) Circ-MAPK4 is also highly expressed in glioma cell lines, especially in U138 and U373, when compared to gial cell line (HA1800). (b) Schematic representation of target sequences of siRNAs which specially silence circ-MAPK4. (c) The silence efficiency of siRNA targeting to circMAPK4 was analyzed by qPCR after transfected for 48 h in either U138 or U373 cells. (d) CCK-8 assays were performed to test survival of U138 and U373 cells after silencing of circ-MAPK4. (e) Colony formation assays were performed to test survival of U138 and U373 cells after silencing of circ-MAPK4. (f) Apoptosis assays were used to detect apoptosis levels of circ-MAPK4 silenced U138 and U373 cells. (g) Western blot assays were performed to analyze the protein expression levels of cleaved form of caspase-9, caspase-7, caspase-3, and PARP1 in circ-MAPK4 silenced U138 and U373 cells. (h) Transwell assays were carried out to test the invasive activity of circ-MAPK4 silenced U138 and U373 cells. The results above were summarized as bar graph. All data are the means ± SEM of three experiments. *P < 0.05; **P < 0.01; ***P < 0.001
false
- WB
CiteAb
Western blot - Anti-GAPDS antibody (AB153802)
Western Blotting using Anti-GAPDS antibody, ab153802. Publication image from He, J. et al., 2020, Mol Cancer, 31992303. Legend direct from paper.
Inhibition of phosphorylation of p38/MAPK reverses cell survival induced by circ-MAPK4. (a) U373 cells transfected with siRNA negative control, circ-MAPK4 siRNA-1 and siRNA-2 were treated with or without p-p38/MAPK inhibitor (SB203580). Inhibition efficiency of p-p38/MAPK inhibitor was accessed by testing phosphorylation and total protein levels of p38/MAPK and ERK using western blot assays. (b, c) CCK-8 and colony formation assays were performed to reveal cell survival of these U373 cells. (d) Apoptosis assays were performed to reveal apoptosis levels of these U373 cells. (e) The western blot assays were used to evaluate effect of p-p38/MAPK inhibitor on protein expression levels of cleaved form of caspase-9, caspase-7, caspase-3, PARP1 in these U373 cells. The data were summarized as bar graph. Data are the means ± SEM of three experiments. *P < 0.05; **P < 0.01; ***P < 0.001
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Reactivity data
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Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
GAPDS plays a critical role in glycolysis serving as an important enzyme that facilitates the conversion of glyceraldehyde-3-phosphate to 13-bisphosphoglycerate. GAPDS can function in complex with other glycolytic enzymes helping generate ATP which is necessary for sperm cell functions. GAPDS expression supports processes essential for male fertility specifically through its involvement in energy supply to sperm flagella.
Pathways
GAPDS is a part of the glycolysis metabolic pathway which is essential for ATP production in sperm. In this pathway it works closely with other glycolytic enzymes like phosphoglycerate kinase and enolase ensuring the continuous flow of energy. GAPDS also indirectly connects to the respiratory chain as glycolytic byproducts feed into mitochondrial oxidative phosphorylation allowing integrated energy metabolism.
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Publications (7)
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Cell cycle (Georgetown, Tex.) 22:347-360 PubMed36281526
2022
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Frontiers in pharmacology 11:547436 PubMed33584252
2021
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Molecular cancer 19:17 PubMed31992303
2020
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Molecular medicine reports 19:2471-2478 PubMed30720094
2019
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International journal of oncology 54:7-16 PubMed30387833
2018
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Oncology reports 38:2843-2851 PubMed29048638
2017
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Molecular cancer 16:151 PubMed28893265
2017
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