RN139 rabbit pAb

RN139 rabbit pAb

AO-06-ES13375-50

RN139 rabbit pAb 50μL

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Antibody Product Overview

ELK.NoES13375
Product nameRN139 rabbit pAb
ReactivityHuman; Mouse
ApplicationsWB;IHC
Other name
Size50μL
Unit price ($)148
Human gene ID11236
Human Swiss-ProtQ8WU17
SourceRabbit
IsotypeIgG
TargetRN139
Fields
Gene nameRNF139 TRC8
Protein nameRN139
Human gene linkView Human Gene
Human Swiss linkView Human Swiss-Prot
Mouse gene ID75841
Mouse gene linkView Mouse Gene
Mouse Swiss-ProtQ7TMV1
Mouse Swiss linkView Mouse Swiss-Prot
Rat gene ID
Rat gene link
Rat Swiss-Prot
Rat Swiss link
ImmunogenSynthesized peptide derived from human RN139 AA range: 10-60
SpecificityThis antibody detects endogenous levels of RN139 at Human/Mouse
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
ClonalityPolyclonal
DilutionWB 1:500-2000;IHC-p 1:50-300
PurificationThe antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen.
Concentration1 mg/ml
Storage stability-20°C/1 year
Molecular Weight (Da)73kD
Observed band (KD)
BackgroundThe protein encoded by this gene is a multi-membrane spanning protein containing a RING-H2 finger. This protein is located in the endoplasmic reticulum, and has been shown to possess ubiquitin ligase activity. This gene was found to be interrupted by a t(3:8) translocation in a family with hereditary renal and non-medulary thyroid cancer. Studies of the Drosophila counterpart suggested that this protein may interact with tumor suppressor protein VHL, as well as with COPS5/JAB1, a protein responsible for the degradation of tumor suppressor CDKN1B/P27KIP. [provided by RefSeq, Jul 2008],
Functiondisease:Defects in RNF139 are a cause of renal cell carcinoma (RCC) [MIM:144700]. A chromosomal aberration involving RNF139 is found in hereditary RCC. Translocation (3;8)(q14.2;q24.1) with FHIT. The result is RNF139 is found to be fused to FHIT and disrupted within the sterol-sensing domain. In contrast, the FHIT coding region is maintained and expressed. Sporadic RCC, where an acquired mutation in RNF139 results in the duplication of 12 nucleotides in the 5'-UTR, has also been identified.,domain:The RING-type zinc finger domain may be essential for ubiquitin ligase activity.,function:Potential tumor suppressor for renal cell carcinoma. Plays a role in mediating ubiquitination. May function as a signaling receptor.,similarity:Contains 1 RING-type zinc finger.,subunit:Interacts with VHL.,tissue specificity:Highly expressed in testis, placenta and adrenal gland. Moderate expression in hea
Subcellular locationEndoplasmic reticulum membrane ; Multi-pass membrane protein .
ExpressionHighly expressed in testis, placenta and adrenal gland. Moderate expression in heart, brain, liver, skeletal muscle and pancreas, and low expression in lung and kidney.

Additional Images

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Western blot analysis of lysates from A431 cells, primary antibody was diluted at 1:1000, 4°over night
Image 2
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Immunohistochemical analysis of paraffin-embedded human Squamous cell carcinoma of lung. 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-ES13375-50
: 10 Produits
Hurry! only 10 items left in stock.

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