PNPLA1 Antibody
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中文名稱：PNPLA1兔多克隆抗體
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貨號：CSB-PA843295LA01HU
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規格：￥440
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圖片：
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Western Blot
All lanes: PNPLA1 antibody at 12μg/ml
Lane 1: Mouse spleen tissue
Lane 2: Mouse skeletal muscle tissue
Secondary
Goat polyclonal to rabbit IgG at 1/10000 dilution
Predicted band size: 58, 48, 49 kDa
Observed band size: 58 kDa -
Immunohistochemistry of paraffin-embedded human kidney tissue using CSB-PA843295LA01HU at dilution of 1:100 -
Immunofluorescent analysis of HepG2 cells using CSB-PA843295LA01HU at dilution of 1:100 and Alexa Fluor 488-congugated AffiniPure Goat Anti-Rabbit IgG(H+L) -
Immunofluorescent analysis of MCF-7 cells using CSB-PA843295LA01HU at dilution of 1:100 and Alexa Fluor 488-congugated AffiniPure Goat Anti-Rabbit IgG(H+L)
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其他：
產品詳情
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產品名稱：Rabbit anti-Homo sapiens (Human) PNPLA1 Polyclonal antibody
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Uniprot No.：
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基因名：PNPLA1
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別名：PNPLA1 antibody; Patatin-like phospholipase domain-containing protein 1 antibody; EC 3.1.1.- antibody
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宿主：Rabbit
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反應種屬：Human, Mouse
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免疫原：Recombinant Human Patatin-like phospholipase domain-containing protein 1 protein (101-300AA)
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免疫原種屬：Homo sapiens (Human)
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標記方式：Non-conjugated
本頁面中的產品，PNPLA1 Antibody (CSB-PA843295LA01HU)，的標記方式是Non-conjugated。對于PNPLA1 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 -
產品提供形式：Liquid
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應用范圍：ELISA, WB, IHC, IF
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推薦稀釋比：
Application Recommended Dilution WB 1:1000-1:5000 IHC 1:20-1:200 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.
產品評價
相關產品
靶點詳情
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功能：Omega-hydroxyceramide transacylase involved in the synthesis of omega-O-acylceramides (esterified omega-hydroxyacyl-sphingosine; EOS), which are extremely hydrophobic lipids involved in skin barrier formation. Catalyzes the last step of the synthesis of omega-O-acylceramides by transferring linoleic acid from triglycerides to an omega-hydroxyceramide. Omega-O-acylceramides, are required for the biogenesis of lipid lamellae in the stratum corneum and the formation of the cornified lipid envelope which are essential for the epidermis barrier function. These lipids also play a role in keratinocyte differentiation. May also act on omega-hydroxylated ultra-long chain fatty acids (omega-OH ULCFA) and acylglucosylceramides (GlcEOS).
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基因功能參考文獻：
- We report two novel PNPLA1 mutations including one novel missense mutation c.335C > A (p.Ser112Tyr) and one novel deletion mutation c.733_735delTAC (p.Tyr245del) in Turkish autosomal recessive congenital ichthyosis patients from unrelated consanguineous families. PMID: 29624231
- PNPLA1 catalyses the omega-O-esterification with linoleic acid to form acylceramides. PMID: 28248300
- PNPLA1 is directly involved in acylceramide synthesis as a transacylase. PMID: 28248318
- The PNPLA1 mutations reportedhere show PNPLA1 to be an important, if relatively rare, cause of ARCI. PMID: 28403545
- The results show potential phenotypic variation in a small percentage of patients with PNPLA1 mutations. The variability of the clinical manifestations and the lack of typical clinical features are specific for patients with PNPLA1 mutations. PMID: 28093717
- Data support that PNPLA1/Pnpla1 is a key player in the formation of omega-O-acylceramide, a crucial process for the epidermal permeability barrier function. PMID: 28369476
- analysis of distinct and previously unreported mutations in the PNPLA1 gene in nine extended consanguineous families with autosomal recessive congenital ichthyosis PMID: 27884779
- an essential role of PNPLA1 in the synthesis of omega-O-AcylCers in human and murine skin. PMID: 27751867
- the variant identified will expand the spectrum of mutations in the PNPLA1 gene, provides more evidence for lack of genotype-phenotype correlation and clinical variability in PNPLA1 and underscores its role in causing autosomal recessive congenital ichthyosis PMID: 26691440
- Letter: novel missense PNPLA1 variant causing autosomal recessive congenital ichthyosis in a Pakistani family. PMID: 26778108
- Results show that PNPLA1 missense mutations observed in this European family affect the patanin-like domain PMID: 24344921
- These results identified hPNPLA1 and a mutant in HeLa cells. PMID: 24057234
- One missense and one nonsense mutation in the catalytic domain of human PNPLA1 were found in six individuals with autosomal recessive congenital ichthyoses from two families. PMID: 22246504
- PNPLA1 exhibited a modest effect on obesity PMID: 19390624
- Observational study of gene-disease association. (HuGE Navigator) PMID: 19390624
- Observational study of gene-disease association and gene-environment interaction. (HuGE Navigator) PMID: 18414634
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相關疾病：Ichthyosis, congenital, autosomal recessive 10 (ARCI10)
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亞細胞定位：Cytoplasm.
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組織特異性：Expressed in the digestive system. Expressed in the epidermis of skin keratinocytes. Strongly expressed in the granular layer. Expressed in the upper epidermis and eccrine sweat glands of the dermis and in the region of keratin filament bundles, which is
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數據庫鏈接：
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