SF-1 rabbit pAb

SF-1 rabbit pAb

AO-06-ES5409-100

SF-1 rabbit pAb 100μL

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Antibody Product Overview

ELK.NoES5409
Product nameSF-1 rabbit pAb
ReactivityHuman;Mouse;Rat
ApplicationsWB;ELISA;IHC
Other nameNR5A1; AD4BP; FTZF1; SF1; Steroidogenic factor 1; SF-1; STF-1; Adrenal 4-binding protein; Fushi tarazu factor homolog 1; Nuclear receptor subfamily 5 group A member 1; Steroid hormone receptor Ad4BP
Size100μL
Unit price ($)248
Human gene ID2516
Human Swiss-ProtQ13285
SourceRabbit
IsotypeIgG
TargetSF-1
Fields>>Cortisol synthesis and secretion;>>Cushing syndrome
Gene nameNR5A1
Protein nameSteroidogenic factor 1
Human gene linkView Human Gene
Human Swiss linkView Human Swiss-Prot
Mouse gene ID26423
Mouse gene linkView Mouse Gene
Mouse Swiss-ProtP33242
Mouse Swiss linkView Mouse Swiss-Prot
Rat gene ID83826
Rat gene linkView Rat Gene
Rat Swiss-ProtP50569
Rat Swiss linkView Rat Swiss-Prot
ImmunogenThe antiserum was produced against synthesized peptide derived from human NR5A1. AA range:169-218
SpecificitySF-1 Polyclonal Antibody detects endogenous levels of SF-1 protein.
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
ClonalityPolyclonal
DilutionWB 1:500-2000;IHC-p 1:50-300; ELISA 2000-20000
PurificationThe antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration1 mg/ml
Storage stability-20°C/1 year
Molecular Weight (Da)
Observed band (KD)50kD
BackgroundThe protein encoded by this gene is a transcriptional activator involved in sex determination. The encoded protein binds DNA as a monomer. Defects in this gene are a cause of XY sex reversal with or without adrenal failure as well as adrenocortical insufficiency without ovarian defect. [provided by RefSeq, Jul 2008],
Functiondisease:Defects in NR5A1 are a cause of adrenocortical insufficiency without ovarian defect [MIM:184757]. The disease is characterized by severe 'slackness,' muscular hypotonia. There is decreased sodium, increased potassium and elevated ACTH.,disease:Defects in NR5A1 are a cause of XY sex reversal with or without adrenal failure [MIM:184757]. This disease is characterized by normal female external genitalia and retention of the uterus.,function:Transcriptional activator. Seems to be essential for sexual differentiation and formation of the primary steroidogenic tissues. Binds to the Ad4 site found in the promoter region of steroidogenic P-450 genes such as CYP11A, CYP11B and CYP21B. Also regulates the Muellerian inhibiting substance (AMH) gene as well as the AHCH and STAR genes. 5'-YCAAGGYC-3' and 5'-RRAGGTCA-3' are the consensus sequences for the recognition by NR5A1/FTZF1. The SFPQ-NO
Subcellular locationNucleus .
ExpressionHigh expressed in the adrenal cortex, the ovary, the testis, and the spleen (PubMed:9177385).

Additional Images

Image 1
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Western blot analysis of lysates from rat lung, using STF-1 Antibody. The lane on the right is blocked with the synthesized peptide.
Image 2
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Immunohistochemical analysis of paraffin-embedded human Colon cancer. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).
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: AO-06-ES5409-100
: 10 Produits
Hurry! only 10 items left in stock.

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