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Rabbit Anti-FOXD2 antibody
Rabbit Anti-FOXD2 antibody
Drosphilia Forkhead Homolog Like 17; FKHL 17; Forkhead box protein D2; Forkhead Related Activator 9; Forkhead-related protein FKHL17; Forkhead-related transcription factor 9; FOXD2; FOXD2_HUMAN; FREAC 9; FREAC-9.
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Details

Product Name FOXD2
Chinese Name 叉头蛋白D2抗体
Alias Drosphilia Forkhead Homolog Like 17; FKHL 17; Forkhead box protein D2; Forkhead Related Activator 9; Forkhead-related protein FKHL17; Forkhead-related transcription factor 9; FOXD2; FOXD2_HUMAN; FREAC 9; FREAC-9.  
Research Area Tumour  Neurobiology  transcriptional regulatory factor  Transporter  Epigenetics  
Immunogen Species Rabbit
Clonality Polyclonal
React Species Human,  (predicted: Mouse, Rat, Pig, Cow, Rabbit, )
Applications WB=1:500-2000 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
Theoretical molecular weight 49kDa
Cellular localization The nucleus 
Form Liquid
Concentration 1mg/ml
immunogen KLH conjugated synthetic peptide derived from human FOXD2: 71-170/495 
Lsotype IgG
Purification affinity purified by Protein A
Buffer Solution 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
Storage Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
Attention This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
Product Detail The FOX family of transcription factors share a common DIUA binding domain termed a winged-helix or forkhead domain. Many FOX proteins play important roles in development, metabolism, cancer and aging. FOXD1 (also designated Brain Factor 2 or BF-2) is involved in regulating inflammation as well as kidney and retinal development. FOXD1 regulates the activity of NF-AT 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:
Probable transcription factor involved in embryogenesis and somatogenesis.

Subcellular Location:
Nucleus.

Tissue Specificity:
Kidney specific.

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

SWISS:
O60548

Gene ID:
2306

Database links:
Entrez Gene: 2306 Human

Entrez Gene: 17301 Mouse

Omim: 602211 Human

SwissProt: O60548 Human

SwissProt: O35392 Mouse

Unigene: 166188 Human

Unigene: 7997 Mouse



Product Picture
Sample:
Jurkat (Human) Cell Lysate at 30 ug
Primary: Anti-FOXD2 (SL21592R) at 1/1000 dilution
Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution
Predicted band size: 49 kD
Observed band size: 49 kD
Sample:
Large intestine (Mouse) Lysate at 40 ug
Primary: Anti- FOXD2 (SL21592R) at 1/1000 dilution
Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution
Predicted band size: 49 kD
Observed band size: 49 kD

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