Anti-DHFR Antibody (CAB1607)
- SKU:
- CAB1607
- Product type:
- Antibody
- Reactivity:
- Human
- Reactivity:
- Mouse
- Host Species:
- Rabbit
- Isotype:
- IgG
- Antibody Type:
- Polyclonal Antibody
- Research Area:
- Immunology
Description
抗体名: | Anti-DHFR Antibody |
抗体コード: | CAB1607 |
抗体サイズ: | 20uL, 50uL, 100uL |
申し込み: | WB IF |
反応性: | Human, Mouse |
宿主種: | Rabbit |
免疫原: | Recombinant fusion protein containing a sequence corresponding to amino acids 1-187 of human DHFR (NP_000782.1). |
申し込み: | WB IF |
推奨希釈: | WB 1:500 - 1:2000 IF 1:50 - 1:200 |
反応性: | Human, Mouse |
ポジティブサンプル: | HeLa, 22Rv1, K-562, HL-60, THP-1, Raji, Mouse liver |
免疫原: | Recombinant fusion protein containing a sequence corresponding to amino acids 1-187 of human DHFR (NP_000782.1). |
精製方法: | Affinity purification |
ストレージバッファ: | Store at -20'C. Avoid freeze / thaw cycles. Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3. |
アイソタイプ: | IgG |
順序: | MVGS LNCI VAVS QNMG IGKN GDLP WPPL RNEF RYFQ RMTT TSSV EGKQ NLVI MGKK TWFS IPEK NRPL KGRI NLVL SREL KEPP QGAH FLSR SLDD ALKL TEQP ELAN KVDM VWIV GGSS VYKE AMNH PGHL KLFV TRIM QDFE SDTF FPEI DLEK YKLL PEYP GVLS DVQE EKGI KYKF EVYE KND |
遺伝子ID: | 1719 |
Uniprot: | P00374 |
セルラーロケーション: | |
計算された分子量: | 15kDa/21kDa |
観察された分子量: | 19kDa |
同義語: | DHFR, DHFRP1, DYR |
バックグラウンド: | Dihydrofolate reductase converts dihydrofolate into tetrahydrofolate, a methyl group shuttle required for the de novo synthesis of purines, thymidylic acid, and certain amino acids. While the functional dihydrofolate reductase gene has been mapped to chromosome 5, multiple intronless processed pseudogenes or dihydrofolate reductase-like genes have been identified on separate chromosomes. Dihydrofolate reductase deficiency has been linked to megaloblastic anemia. Several transcript variants encoding different isoforms have been found for this gene. |
UniProt Protein Function: | DHFR: Key enzyme in folate metabolism. Contributes to the de novo mitochondrial thymidylate biosynthesis pathway. Catalyzes an essential reaction for de novo glycine and purine synthesis, and for DNA precursor synthesis. Binds its own mRNA and that of DHFRL1. Defects in DHFR are the cause of megaloblastic anemia due to dihydrofolate reductase deficiency (DHFRD). DHFRD is an inborn error of metabolism, characterized by megaloblastic anemia and/or pancytopenia, severe cerebral folate deficiency, and cerebral tetrahydrobiopterin deficiency. Clinical features include variable neurologic symptoms, ranging from severe developmental delay and generalized seizures in infancy, to childhood absence epilepsy with learning difficulties, to lack of symptoms. Belongs to the dihydrofolate reductase family. |
UniProt Protein Details: | Protein type:Cofactor and Vitamin Metabolism - one carbon pool by folate; Oxidoreductase; EC 1.5.1.3; Cofactor and Vitamin Metabolism - folate biosynthesis Chromosomal Location of Human Ortholog: 5q14.1 Cellular Component: nucleoplasm; cytosol Molecular Function:mRNA binding; drug binding; dihydrofolate reductase activity; NADP binding Biological Process: tetrahydrofolate metabolic process; vitamin metabolic process; one-carbon compound metabolic process; nitric oxide metabolic process; G1/S-specific transcription in mitotic cell cycle; tetrahydrofolate biosynthetic process; nucleotide biosynthetic process; response to methotrexate; regulation of nitric-oxide synthase activity; folic acid metabolic process; mitotic cell cycle; glycine biosynthetic process; water-soluble vitamin metabolic process; G1/S transition of mitotic cell cycle Disease: Megaloblastic Anemia Due To Dihydrofolate Reductase Deficiency |
UniProt Code: | P00374 |
NCBI GenInfo Identifier: | 118992 |
NCBI Gene ID: | |
NCBI Accession: | P00374.2 |
Molecular Weight: | |
NCBI Full Name: | Dihydrofolate reductase |
UniProt Protein Name: | Dihydrofolate reductase |
Protein Family: | Viral dihydrofolate reductase |
UniProt Gene Name: | DHFR |
UniProt Entry Name: | DYR_HUMAN |