PMM1 Antibody
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中文名稱:PMM1兔多克隆抗體
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貨號:CSB-PA018237LA01HU
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規(guī)格:¥440
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促銷:
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圖片:
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Western blot
All lanes: PMM1 antibody at 2µg/ml
Lane 1: HepG2 whole cell lysate
Lane 2: NIH/3T3 whole cell lysate
Lane 3: 293T whole cell lysate
Lane 4: Mouse brain tissue
Secondary
Goat polyclonal to rabbit IgG at 1/10000 dilution
Predicted band size: 30 kDa
Observed band size: 30 kDa -
Immunohistochemistry of paraffin-embedded human pancreatic tissue using CSB-PA018237LA01HU at dilution of 1:100
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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) PMM1 Polyclonal antibody
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Uniprot No.:
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基因名:PMM1
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別名:Brain glucose-1,6-bisphosphatase antibody; Phosphomannomutase 1 antibody; PMM 1 antibody; pmm1 antibody; PMM1_HUMAN antibody; PMMH 22 antibody; PMMH-22 antibody; PMMH22 antibody; Sec53 antibody
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宿主:Rabbit
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反應(yīng)種屬:Human, Mouse
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免疫原:Recombinant Human Phosphomannomutase 1 protein (2-262AA)
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免疫原種屬:Homo sapiens (Human)
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標(biāo)記方式:Non-conjugated
本頁面中的產(chǎn)品,PMM1 Antibody (CSB-PA018237LA01HU),的標(biāo)記方式是Non-conjugated。對于PMM1 Antibody,我們還提供其他標(biāo)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(yīng)用范圍:ELISA, WB, IHC
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推薦稀釋比:
Application Recommended Dilution WB 1:500-1:5000 IHC 1:20-1:200 -
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.
相關(guān)產(chǎn)品
靶點詳情
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功能:Involved in the synthesis of the GDP-mannose and dolichol-phosphate-mannose required for a number of critical mannosyl transfer reactions. In addition, may be responsible for the degradation of glucose-1,6-bisphosphate in ischemic brain.
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基因功能參考文獻(xiàn):
- a triple mutant of phospomannomutase1 that retains mutase and phosphatase activity, but is unable to bind inosine monophosphate, was characterized. PMID: 29261720
- Mutations in phosphomannomutase is associated with ophthalmic manifestations of congenital disorder of glycosylation type 1a PMID: 12789572
- human alpha-phosphomannomutase 1 crystallographic structure reveals the structural basis of congenital disorder of glycosylation type 1a PMID: 16540464
- analysis of mental development in a patient with phosphomannomutase deficiency who is compound heterozygous for T237R/C241S mutations [case report] PMID: 17186415
- The genes GUS and PMM1 are recommended for normalization purposes in gene expression studies of liver tissue from patients with chronic hepatitis. PMID: 18591914
- PMM1 is responsible for the degradation of Glc-1,6-P(2) in brain PMID: 18927083
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亞細(xì)胞定位:Cytoplasm.
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蛋白家族:Eukaryotic PMM family
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組織特異性:Strong expression in liver, heart, brain, and pancreas; lower expression in skeletal muscle.
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數(shù)據(jù)庫鏈接:
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