Ribosomal Protein L11 rabbit pAb

Ribosomal Protein L11 rabbit pAb

AO-06-ES7068-50

Ribosomal Protein L11 rabbit pAb 50μL

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Antibody Product Overview

ELK.NoES7068
Product nameRibosomal Protein L11 rabbit pAb
ReactivityHuman;Mouse;Rat
ApplicationsWB;ELISA;IHC
Other nameRPL11; 60S ribosomal protein L11; CLL-associated antigen KW-12
Size50μL
Unit price ($)148
Human gene ID6135
Human Swiss-ProtP62913
SourceRabbit
IsotypeIgG
TargetRibosomal Protein L11
Fields>>Ribosome;>>Coronavirus disease - COVID-19
Gene nameRPL11
Protein name60S ribosomal protein L11
Human gene linkView Human Gene
Human Swiss linkView Human Swiss-Prot
Mouse gene ID67025
Mouse gene linkView Mouse Gene
Mouse Swiss-ProtQ9CXW4
Mouse Swiss linkView Mouse Swiss-Prot
Rat gene ID
Rat gene link
Rat Swiss-ProtP62914
Rat Swiss linkView Rat Swiss-Prot
ImmunogenSynthesized peptide derived from Ribosomal Protein L11 . at AA range: 100-180
SpecificityRibosomal Protein L11 Polyclonal Antibody detects endogenous levels of Ribosomal Protein L11 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)20kD
BackgroundRibosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 60S subunit. The protein belongs to the L5P family of ribosomal proteins. It is located in the cytoplasm. The protein probably associates with the 5S rRNA. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Dec 2010],
Functiondisease:Defects in RPL11 are the cause of Diamond-Blackfan anemia type 7 (DBA7) [MIM:612562]. DBA7 is a form of Diamond-Blackfan anemia, a congenital non-regenerative hypoplastic anemia that usually presents early in infancy. Diamond-Blackfan anemia is characterized by a moderate to severe macrocytic anemia, erythroblastopenia, and an increased risk of malignancy. 30 to 40% of Diamond-Blackfan anemia patients present with short stature and congenital anomalies, the most frequent being craniofacial (Pierre-Robin syndrome and cleft palate), thumb and urogenital anomalies.,function:Binds to 5S ribosomal RNA (By similarity). Required for rRNA maturation and formation of the 60S ribosomal subunits.,similarity:Belongs to the ribosomal protein L5P family.,
Subcellular locationNucleus, nucleolus . Cytoplasm .
ExpressionAmygdala,Cervix carcinoma,Tonsil,

Additional Images

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Western blot analysis of lysates from A431 cells, primary antibody was diluted at 1:1000, 4°over night
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Immunohistochemical analysis of paraffin-embedded human lung 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-ES7068-50
: 10 Produits
Hurry! only 10 items left in stock.

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