TRAPPC11 Antibody
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中文名稱:TRAPPC11兔多克隆抗體
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貨號:CSB-PA801799LA01HU
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規(guī)格:¥440
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圖片:
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Immunofluorescence staining of U251 cells with CSB-PA801799LA01HU at 1:100, counter-stained with DAPI. The cells were fixed in 4% formaldehyde, permeabilized using 0.2% Triton X-100 and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4°C. The secondary antibody was Alexa Fluor 488-congugated AffiniPure Goat Anti-Rabbit IgG(H+L).
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其他:
產(chǎn)品詳情
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產(chǎn)品名稱:Rabbit anti-Homo sapiens (Human) TRAPPC11 Polyclonal antibody
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Uniprot No.:
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基因名:TRAPPC11
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別名:TRAPPC11 antibody; C4orf41 antibody; Trafficking protein particle complex subunit 11 antibody
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宿主:Rabbit
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反應種屬:Human
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免疫原:Recombinant Human Trafficking protein particle complex subunit 11 protein (704-836AA)
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免疫原種屬:Homo sapiens (Human)
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標記方式:Non-conjugated
本頁面中的產(chǎn)品,TRAPPC11 Antibody (CSB-PA801799LA01HU),的標記方式是Non-conjugated。對于TRAPPC11 Antibody,我們還提供其他標記。見下表:
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克隆類型:Polyclonal
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抗體亞型:IgG
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純化方式:>95%, Protein G purified
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濃度:It differs from different batches. Please contact us to confirm it.
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保存緩沖液:Preservative: 0.03% Proclin 300
Constituents: 50% Glycerol, 0.01M PBS, pH 7.4 -
產(chǎn)品提供形式:Liquid
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應用范圍:ELISA, IF
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推薦稀釋比:
Application Recommended Dilution IF 1:50-1:200 -
Protocols:
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儲存條件:Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
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貨期:Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.
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用途:For Research Use Only. Not for use in diagnostic or therapeutic procedures.
相關產(chǎn)品
靶點詳情
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功能:Involved in endoplasmic reticulum to Golgi apparatus trafficking at a very early stage.
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基因功能參考文獻:
- Recessive mutations in TRAPPC11 and GOSR2 are associated with congenital muscular dystrophy and hypoglycosylation of alpha-dystroglycan. PMID: 29855340
- The identified novel TRAPPC11 mutation represents an expansion of the myopathy phenotype described before and is characterised particularly by achalasia, alacrima, neurological and muscular phenotypes. PMID: 27707803
- TRAPPC11 role in protein glycosylation and lipid-linked oligosaccharides biosynthesis PMID: 26912795
- Homozygous mutations in the membrane trafficking component TRAPPC11 causes a form of autosomal-recessive, slowly progressive limb girdle muscular dystrophy with childhood onset and high serum creatine kinase. PMID: 23830518
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相關疾?。?/div>Limb-girdle muscular dystrophy 2S (LGMD2S)亞細胞定位:Golgi apparatus. Golgi apparatus, cis-Golgi network.蛋白家族:TRAPPC11 family數(shù)據(jù)庫鏈接:
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