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Anti-C11orf71 antibody (bs-9941R)

Anti-C11orf71 antibody (bs-9941R)

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Anti-C11orf71 antibody

英文名称C11orf71
中文名称11号染色体开放阅读框71抗体
别    名C11orf71 chromosome 11 open reading frame 71; CK071_HUMAN; FLJ20010; Gm5617; hypothetical protein LOC54494; Uncharacterized protein C11orf71.

DATASHEET

Host:Rabbit

Target Protein:C11orf71

IR:Immunogen Range:1-100/123

Clonality:Polyclonal

Isotype:IgG

Entrez Gene:54494

Swiss Prot:Q6IPW1

Source:KLH conjugated synthetic peptide derived from human C11orf71:1-100/123 

Purification:affinity purified by Protein A

Storage:0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol. Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.

Background:C11orf71, also known as FLJ20010, is a 123 amino acid protein that exists as two alternatively spliced isoforms and is encoded by a gene located on human chromosome 11. With approximately 135 million base pairs and 1,400 genes, chromosome 11 makes up around 4% of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and β thalassemia are caused by HBB gene mutations. Wilms' tumors, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11.

Size:100ul

Concentration:1mg/ml

Applications:WB(1:500-2000)
ELISA(1:5000-10000)
IHC-P(1:100-500)
IHC-F(1:100-500)
IF(1:50-200)

Cross Reactive Species:Human
.

For research use only. Not intended for diagnostic or therapeutic use.

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Anti-C11orf71 antibody (bs-994...

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