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FOXD1 Rabbit pAb (bs-12193R)  
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50ul/1180.00元
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200ul/2800.00元
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產品編號 bs-12193R
英文名稱 FOXD1 Rabbit pAb
中文名稱 叉頭蛋白D1抗體
別    名 Brain Factor 2; FKH L8; FKHL 8; FKHL8; Forkhead(Drosophila) like 8; Forkhead box D1; Forkhead box protein D1; Forkhead drosophila homolog like 8; Forkhead like 8; Forkhead related activator 4; Forkhead related protein FKHL8; Forkhead related transcription  
Specific References  (2)     |     bs-12193R has been referenced in 2 publications.
[IF=5.682] Gao, Cao. et al. BMSC-Derived Exosomes Carrying lncRNA-ZFAS1 Alleviate Pulmonary Ischemia/Reperfusion Injury by UPF1-Mediated mRNA Decay of FOXD1. MOL NEUROBIOL. 2023 Jan;:1-18  WB ;  Mouse.  
[IF=3.399] Qi Liu. et al. Investigation of Candidate Genes and Pathways in Basal/TNBC Patients by Integrated Analysis:. Technol Cancer Res T. 2021;():  IHC ;  Human.  
研究領域 細胞生物  發育生物學  神經生物學  干細胞  轉錄調節因子  細胞分化  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 (predicted: Human,Mouse,Rabbit,Sheep,Chicken,Dog)
產品應用 WB=1:500-2000,IHC-P=1:100-500,IHC-F=1:100-500,IF=1:100-500,ICC/IF=1:100-500,ELISA=1:5000-10000
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理論分子量 46 kDa
檢測分子量
細胞定位 細胞核 
性    狀 Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from Human FOXD1: 131-230/465 
亞    型 IgG
純化方法 affinity purified by Protein A
緩 沖 液 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
保存條件 Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
注意事項 This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
產品介紹 FOXD1 is involved in regulating inflammation as well as kidney and retinal development. FOXD1 regulates the activity of NFAT and NFkB. Deficiency of FOXD1 results in multiorgan systemic inflammation, exaggerated Th cell-derived cytokine production, and T cell proliferation in autogolgous MLRs. In kidneys, FOXD1 controls the production of signals required for the normal transition of induced mesenchyme into tubular epithelium and full growth and branching of the collecting system. Deletion of FOXD1 results in renal abnormalities. FOXD2 acts as a modulator of T cell activation.

Function:
Transcription factor required for formation of positional identity in the developing retina, regionalization of the optic chiasm and morphogenesis of the kidney. Can neuralize ectodermal cells directly.

Subcellular Location:
Nucleus.

Similarity:
Contains 1 fork-head DNA-binding domain.

SWISS:
Q16676

Gene ID:
2297

Database links:

Entrez Gene: 2297 Human

Entrez Gene: 15229 Mouse

GenBank: NP_004463 Human

Omim: 601091 Human

SwissProt: Q16676 Human

SwissProt: Q61345 Mouse

Unigene: 519385 Human

Unigene: 347441 Mouse



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