PEX2 Antibody
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中文名稱：PEX2兔多克隆抗體
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貨號：CSB-PA985453
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規格：￥2024
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圖片：
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Western blot analysis of extracts from A549 cells, using PXMP3 antibody. -
Immunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue using PXMP3 antibody.
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其他：
產品詳情
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產品名稱：Rabbit anti-Homo sapiens (Human) PEX2 Polyclonal antibody
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Uniprot No.：
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基因名：PEX2
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別名：PEX2; PAF1; PMP3; PMP35; PXMP3; RNF72; Peroxisome biogenesis factor 2; 35 kDa peroxisomal membrane protein; Peroxin-2; Peroxisomal membrane protein 3; Peroxisome assembly factor 1; PAF-1; RING finger protein 72
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宿主：Rabbit
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反應種屬：Human
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免疫原：Synthesized peptide derived from N-terminal of Human PXMP3.
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免疫原種屬：Homo sapiens (Human)
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克隆類型：Polyclonal
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純化方式：The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
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濃度：It differs from different batches. Please contact us to confirm it.
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產品提供形式：Liquid
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應用范圍：ELISA,WB,IHC
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推薦稀釋比：
Application Recommended Dilution WB 1:500-1:3000 IHC 1:50-1:100 -
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.
產品評價
相關產品
靶點詳情
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功能：Somewhat implicated in the biogenesis of peroxisomes.
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基因功能參考文獻：
- PEX2 is required for peroxisome autophagy during starvation. PMID: 27597759
- the carrier frequencies for two PEX2 mutations causative of the severe Zellweger syndrome spectrum phenotype in Ashkenazi Jews PMID: 23590336
- Ischemic wound healing is retarded in mice subjected to recombinant PEX2 injections or viral transduction with PEX2-lentivurus. PMID: 21903356
- Genetic screening of PEX2 and other PEX genes involved in peroxisomal biogenesis is warranted in children and adults with ARCA PMID: 21392394
- The cause of the syndrome in this patient was a point mutation that resulted in the premature termination of peroxisome assembly factor-1. PMID: 1546315
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相關疾病：Peroxisome biogenesis disorder complementation group 5 (PBD-CG5); Peroxisome biogenesis disorder 5A (PBD5A); Peroxisome biogenesis disorder 5B (PBD5B)
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亞細胞定位：Peroxisome membrane; Multi-pass membrane protein.
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蛋白家族：Pex2/pex10/pex12 family
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數據庫鏈接：
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