CYP26C1 Antibody
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								中文名稱:CYP26C1兔多克隆抗體
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								貨號:CSB-PA009422
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								規(guī)格:¥1090
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								其他:
產(chǎn)品詳情
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											Uniprot No.:
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											基因名:CYP26C1
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											別名:CP26C_HUMAN antibody; cyp26b1l antibody; CYP26C1 antibody; cyp26d1 antibody; Cytochrome P450 26C1 antibody; Cytochrome P450 family 26 subfamily C polypeptide 1 antibody; Cytochrome P450; subfamily XXVIC polypeptide 1 antibody; EG546726 antibody; FFDD4 antibody; FLJ45301 antibody; MGC158120 antibody; retinoic acid catabolizing enzyme antibody
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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 the N-terminal region of Human CYP26C1.
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											免疫原種屬:Homo sapiens (Human)
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											標記方式:Non-conjugated
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											抗體亞型:IgG
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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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											保存緩沖液:Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
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											產(chǎn)品提供形式:Liquid
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											應用范圍:IHC, ELISA
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											推薦稀釋比:Application Recommended Dilution IHC 1:100-1:300 ELISA 1:40000 
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											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(guān)產(chǎn)品
靶點詳情
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											功能:Plays a role in retinoic acid metabolism. Acts on retinoids, including all-trans-retinoic acid (RA) and its stereoisomer 9-cis-RA (preferred substrate).
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											基因功能參考文獻:- Together, these findings describe CYP26C1 as the first genetic modifier for SHOX deficiency. PMID: 27861128
- Elevated expression of CYP26C1 in primary breast carcinomas PMID: 26009309
- Focal facial dermal dysplasia, type IV results from the loss of function mutations in CYP26C1. PMID: 23161670
- CYP26A1 and CYP26C1 play a pivotal role in the pathogenesis of nonsyndromic bilateral and unilateral optic nerve aplasia. PMID: 21850183
- may play a specific role in catabolizing both all-trans and 9-cis isomers of retinoic acid. PMID: 14532297
- Observational study of gene-disease association. (HuGE Navigator) PMID: 16385451
- Observational study of gene-disease association and gene-gene interaction. (HuGE Navigator) PMID: 19703508
- Observational study of gene-disease association. (HuGE Navigator) PMID: 16933217
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											相關(guān)疾?。?/div>Focal facial dermal dysplasia 4 (FFDD4)亞細胞定位:Membrane; Single-pass membrane protein.蛋白家族:Cytochrome P450 family組織特異性:Detected in most tissues at very low level.數(shù)據(jù)庫鏈接:
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