Anti-Drosophila FMR1抗体[6A15]
小鼠单克隆抗体[6A15] to Drosophila FMR1
Mouse
适用于: ELISA, ICC/IF, IP, WBmore details
与反应: Drosophila melanogaster
不与反应: Human
Recombinant fragment (His-tag) corresponding to Drosophila melanogaster Drosophila FMR1. N-terminal His tag-dFMR1 (C-terminal 580aa).
Database link: Q9NFU0
Fragile X syndrome is the most common inherited form of mental retardation. It is caused by loss of FMR1 gene activity due to either lack of expression or expression of a mutant form of the protein. In mammals, FMR1 is a member of a small protein family that consists of FMR1, FXR1, and FXR2. All three members bind RNA and contain sequence motifs that are commonly found in RNA-binding proteins, including two KH domains and an RGG box.The Drosophila genome contains a single gene homologous to the FXR family. dFMR1 is subjected to transcriptional and posttranscriptional regulation during development and it homomerizes, like its human counterpart. dFMR1 profile of expression recapitulates that of the human FXR protein family: it is highly enriched in muscles, in central nervous system and in gonads. In the larval brain, anti-dFMR1 also recognizes mushroom bodies, a centre that mediates learning and memory. These features make the fly an ideal system to analyse the role of the FXR family and to identify genes in the FMRP pathway.
The Life Science industry has been in the grips of a reproducibility crisis for a number of years. Abcam is leading the way in addressing this with our range of recombinant monoclonal antibodies and knockout edited cell lines for gold-standard validation. Please check that this product meets your needs before purchasing.
If you have any questions, special requirements or concerns, please send us an inquiry and/or contact our Support team ahead of purchase. Recommended alternatives for this product can be found below, along with publications, customer reviews and Q&As
Liquid
Shipped at 4°C. Upon delivery aliquot and store at -20°C or -80°C. Avoid repeated freeze / thaw cycles.
Preservative: 0.1% Sodium azide
Constituent: PBS
浓度
100 µl 浓度为 1 mg/ml
Protein A purified
Protein A purified from tissue culture supernatant.
Fragile X syndrome is the most common inherited form of mental retardation. It is caused by loss of FMR1 gene activity due to either lack of expression or expression of a mutant form of the protein. In mammals, FMR1 is a member of a small protein family that consists of FMR1, FXR1, and FXR2. All three members bind RNA and contain sequence motifs that are commonly found in RNA-binding proteins, including two KH domains and an RGG box.The Drosophila genome contains a single gene homologous to the FXR family. dFMR1 is subjected to transcriptional and posttranscriptional regulation during development and it homomerizes, like its human counterpart. dFMR1 profile of expression recapitulates that of the human FXR protein family: it is highly enriched in muscles, in central nervous system and in gonads. In the larval brain, anti-dFMR1 also recognizes mushroom bodies, a centre that mediates learning and memory. These features make the fly an ideal system to analyse the role of the FXR family and to identify genes in the FMRP pathway.
单克隆
6A15
Sp2/0
IgG1
Abpromise™承诺保证使用ab10299于以下的经测试应用
“应用说明”部分 下显示的仅为推荐的起始稀释度;实际最佳的稀释度/浓度应由使用者检定。
应用 | Ab评论 | 说明 |
---|---|---|
ELISA | Use at an assay dependent concentration. | |
ICC/IF | Use at an assay dependent concentration. | |
IP | (1) | Use at an assay dependent concentration. See Abreview. |
WB | Use at an assay dependent concentration. |
Entrez Gene: 37528 Drosophila melanogaster
SwissProt: Q9NFU0 Drosophila melanogaster
hide
Drosophila fragile X mental retardation protein antibody
fragile X mental retardation protein antibody
dFMR antibody
dFMR1 antibody
dFXR antibody