CYP4F22 Antibody
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货号:CSB-PA740654LA01HU
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规格:¥440
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促销:
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图片:
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Western Blot
Positive WB detected in: HEK293 whole cell lysate, Hela whole cell lysate, MCF-7 whole cell lysate, HepG2 whole cell lysate, A549 whole cell lysate
All lanes: CYP4F22 antibody at 3.2µg/ml
Secondary
Goat polyclonal to rabbit IgG at 1/50000 dilution
Predicted band size: 62 kDa
Observed band size: 62 kDa
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其他:
产品详情
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产品名称:Rabbit anti-Homo sapiens (Human) CYP4F22 Polyclonal antibody
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Uniprot No.:Q6NT55
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基因名:CYP4F22
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别名:CYP4F22Cytochrome P450 4F22 antibody; EC 1.14.14.- antibody
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宿主:Rabbit
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反应种属:Human
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免疫原:Recombinant Human Cytochrome P450 4F22 protein (413-507AA)
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免疫原种属:Homo sapiens (Human)
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标记方式:Non-conjugated
本页面中的产品,CYP4F22 Antibody (CSB-PA740654LA01HU),的标记方式是Non-conjugated。对于CYP4F22 Antibody,我们还提供其他标记。见下表:
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克隆类型:Polyclonal
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抗体亚型:IgG
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纯化方式:>95%, Protein G purified
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浓度:It differs from different batches. Please contact us to confirm it.
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保存缓冲液:Preservative: 0.03% Proclin 300
Constituents: 50% Glycerol, 0.01M PBS, pH 7.4 -
产品提供形式:Liquid
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应用范围:ELISA, WB
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推荐稀释比:
Application Recommended Dilution WB 1:500-1:5000 -
Protocols:
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储存条件:Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
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货期: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.
相关产品
靶点详情
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功能:A cytochrome P450 monooxygenase involved in epidermal ceramide biosynthesis. Hydroxylates the terminal carbon (omega-hydroxylation) of ultra-long-chain fatty acyls (C28-C36) prior to ceramide synthesis. Contributes to the synthesis of three classes of omega-hydroxy-ultra-long chain fatty acylceramides having sphingosine, 6-hydroxysphingosine and phytosphingosine bases, all major lipid components that underlie the permeability barrier of the stratum corneum. Mechanistically, uses molecular oxygen inserting one oxygen atom into a substrate, and reducing the second into a water molecule, with two electrons provided by NADPH via cytochrome P450 reductase (CPR; NADPH-ferrihemoprotein reductase).
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基因功能参考文献:
- patients carrying one or two truncating CYP4F22 mutations affecting the SBRs tend to develop collodion membrane at birth PMID: 27735052
- We report two cases of Congenital Ichthyosiform Erythroderma showing homozygous mutations in the gene CYP4F22. PMID: 26646773
- description of CYP4F22 mutations from a Japanese collodion baby with lamellar ichthyosis [case report] PMID: 23871423
- Letter: CYP4F22 is highly expressed at the site and timing of onset of keratinization during skin development. PMID: 22209317
- REVIEW: genetic analyses have identified a wide spectrum of mutations in the CYP4V2gene from patients suffering from Bietti's crystalline corneoretinal dystrophy, and mutations in theCYP4F22 gene have been linked to lamellar ichthyosis PMID: 21540472
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相关疾病:Ichthyosis, congenital, autosomal recessive 5 (ARCI5)
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亚细胞定位:Endoplasmic reticulum membrane; Single-pass type I membrane protein. Microsome membrane; Single-pass type I membrane protein.
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蛋白家族:Cytochrome P450 family
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数据库链接:
HGNC: 26820
OMIM: 604777
KEGG: hsa:126410
STRING: 9606.ENSP00000269703
UniGene: Hs.156452
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