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Mouse Anti-MTHFD1L (AA 801-900) Recombinant Antibody (CBXF-1011) (CBMAB-F0309-CQ)


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Summary

Host Animal
Mouse
Specificity
Human
Clone
CBXF-1011
Antibody Isotype
IgG2a
Application
ELISA, WB

Basic Information

Specificity
Human
Antibody Isotype
IgG2a
Application Notes
The COA includes recommended starting dilutions, optimal dilutions should be determined by the end user.

Formulations & Storage [For reference only, actual COA shall prevail!]

Format
Liquid
Buffer
PBS, pH 7.2
Preservative
0.09% sodium azide
Storage
Store at +4°C short term (1-2 weeks). Aliquot and store at -20°C long term. Avoid repeated freeze/thaw cycles.
Epitope
AA 801-900

Target

Full Name
Methylenetetrahydrofolate Dehydrogenase (NADP+ Dependent) 1 Like
Introduction
The protein encoded by this gene is involved in the synthesis of tetrahydrofolate (THF) in the mitochondrion. THF is important in the de novo synthesis of purines and thymidylate and in the regeneration of methionine from homocysteine. Several transcript variants encoding different isoforms have been found for this gene.
Entrez Gene ID
25902
UniProt ID
Q6UB35
Alternative Names
Methylenetetrahydrofolate Dehydrogenase (NADP+ Dependent) 1 Like; Monofunctional C1-Tetrahydrofolate Synthase, Mitochondrial; Formyltetrahydrofolate Synthetase Domain Containing 1; 10-Formyl-THF Synthetase; EC 6.3.4.3; FTHFSDC1;
Function
May provide the missing metabolic reaction required to link the mitochondria and the cytoplasm in the mammalian model of one-carbon folate metabolism complementing thus the enzymatic activities of MTHFD2.
Biological Process
10-formyltetrahydrofolate biosynthetic process Source: BHF-UCL
Embryonic neurocranium morphogenesis Source: BHF-UCL
Embryonic viscerocranium morphogenesis Source: BHF-UCL
Folic acid-containing compound metabolic process Source: BHF-UCL
Formate metabolic process Source: BHF-UCL
Neural tube closure Source: BHF-UCL
Tetrahydrofolate interconversion Source: GO_Central
Cellular Location
Mitochondrion
More Infomation

Green, A. C., Marttila, P., Kiweler, N., Chalkiadaki, C., Wiita, E., Cookson, V., ... & Meiser, J. (2023). Formate overflow drives toxic folate trapping in MTHFD1 inhibited cancer cells. Nature Metabolism, 5(4), 642-659.

Rao, K., Zheng, K., Zhao, Q., He, J., Zhou, B., Hou, G., ... & Xia, Q. (2023). The negative effect of G1958A polymorphism on MTHFD1 protein stability and HCC growth. Cellular Oncology, 46(3), 735-744.

Meng, Q., Lu, Y. X., Wei, C., Wang, Z. X., Lin, J. F., Liao, K., ... & Ju, H. Q. (2022). Arginine methylation of MTHFD1 by PRMT5 enhances anoikis resistance and cancer metastasis. Oncogene, 41(32), 3912-3924.

Vohra, M., Adhikari, P., CD, S., Nagri, S. K., Umakanth, S., Satyamoorthy, K., & Rai, P. S. (2020). CpG-SNP site methylation regulates allele-specific expression of MTHFD1 gene in type 2 diabetes. Laboratory Investigation, 100(8), 1090-1101.

Bidla, G., Watkins, D., Chéry, C., Froese, D. S., Ells, C., Kerachian, M., ... & Rosenblatt, D. S. (2020). Biochemical analysis of patients with mutations in MTHFD1 and a diagnosis of methylenetetrahydrofolate dehydrogenase 1 deficiency. Molecular Genetics and Metabolism, 130(3), 179-182.

Xu, M., Li, J., Chen, X., Han, L., Li, L., & Liu, Y. (2019). MTHFD1 promoter hypermethylation increases the risk of hypertension. Clinical and Experimental Hypertension, 41(5), 422-427.

Sdelci, S., Rendeiro, A. F., Rathert, P., You, W., Lin, J. M. G., Ringler, A., ... & Kubicek, S. (2019). MTHFD1 interaction with BRD4 links folate metabolism to transcriptional regulation. Nature genetics, 51(6), 990-998.

Yu, H., Wang, H., Xu, H. R., Zhang, Y. C., Yu, X. B., Wu, M. C., ... & Cong, W. M. (2019). Overexpression of MTHFD1 in hepatocellular carcinoma predicts poorer survival and recurrence. Future Oncology, 15(15), 1771-1780.

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For research use only. Not intended for any clinical use.

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