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FoxD3 Rabbit Polyclonal Antibody

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产品基本信息

产品货号
BD-PT1743
产品名称
FoxD3 Rabbit Polyclonal Antibody
别名
FOXD3; HFH2; Forkhead box protein D3; HNF3/FH transcription factor genesis
类别
常规抗体
基因名称
FOXD3
蛋白名称
Forkhead box protein D3
推荐应用
WB
反应种属
Human,Mouse
浓度
1 mg/ml
存储缓冲液
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% New type preservative N.
Human Gene ID
27022
Human Gene Link
http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=27022
Human Swissprot No.
Q9UJU5
Human Swissprot Link
http://www.uniprot.org/uniprotkb/Q9UJU5/entry
Mouse Gene ID
15221
Mouse Gene Link
http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=15221
Mouse Swissprot No.
Q61060
Mouse Swissprot Link
http://www.uniprot.org/uniprot/Q61060
免疫原
The antiserum was produced against synthesized peptide derived from human FOXD3. AA range:211-260
特异性
FoxD3 Polyclonal Antibody detects endogenous levels of FoxD3 protein.
稀释度
WB 1:500 - 1:2000. IHC 1:100 - 1:300. ELISA: 1:5000.. IF 1:50-200
预测分子量
48kD
运输及保存条件
-20°C/1 year
宿主
Polyclonal, Rabbit,IgG
背景介绍
This gene belongs to the forkhead family of transcription factors which is characterized by a distinct forkhead domain. Mutations in this gene cause autoimmune susceptibility 1. [provided by RefSeq, Nov 2008],
组织表达
Expressed in chronic myeloid leukemia, Jurkat T-cell leukemia and teratocarcinoma cell lines, but not in any other cell lines or normal tissues examined.
细胞定位
Nucleus .
功能
disease:Defects in FOXD3 are associated with susceptibility to autoimmune disease type 1 (AIS1) [MIM:607836]; also called vitiligo-associated multiple autoimmune disease susceptibility type 2 (VAMAS2). Generalized vitiligo is an acquired disorder in which white patches of skin and hair result from autoimmune loss of melanocytes, often associated with other autoimmune disorders. Most cases occur in a sporadic family pattern suggesting polygenic, multifactorial inheritance. However, a striking family in which a somewhat unusual vitiligo phenotype has been described, characterized by progressively coalescent diffuse depigmentation and relatively early disease onset, segregated as an apparent autosomal dominant with incomplete penetrance.,function:Binds to the consensus sequence 5'-A[AT]T[AG]TTTGTTT-3' and acts as a transcriptional repressor. Also acts as a transcriptional activator. Promotes development of neural crest cells from neural tube progenitors. Restricts neural progenitor cells to the neural crest lineage while suppressing interneuron differentiation. Required for maintenance of pluripotent cells in the pre-implantation and peri-implantation stages of embryogenesis.,similarity:Contains 1 fork-head DNA-binding domain.,tissue specificity:Expressed in chronic myeloid leukemia, Jurkat T-cell leukemia and teratocarcinoma cell lines, but not in any other cell lines or normal tissues examined.,
期货
现货
纯化
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Immunohistochemistry analysis of paraffin-embedded human heart tissue, using FOXD3 Antibody. The picture on the right is blocked with the synthesized peptide.

Western blot analysis of lysates from HUVEC and 293 cells, using FOXD3 Antibody. The lane on the right is blocked with the synthesized peptide.

Western Blot analysis of various cells using FoxD3 Polyclonal Antibody cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit (SC-003,Inventbiotech,MN,USA).

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