SLC33A1 Antibody
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								中文名稱:SLC33A1兔多克隆抗體
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								貨號:CSB-PA238172
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								規(guī)格:¥1100
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								圖片:
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								其他:
產(chǎn)品詳情
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											Uniprot No.:
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											基因名:SLC33A1
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											別名:ACATN antibody; ACATN_HUMAN antibody; Acetyl CoA transporter antibody; Acetyl Coenzyme A transporter antibody; Acetyl coenzyme A transporter 1 antibody; Acetyl-CoA transporter 1 antibody; Acetyl-coenzyme A transporter 1 antibody; AT 1 antibody; AT-1 antibody; AT1 antibody; Human Angiotensin II Type 1 Receptor antibody; Slc33a1 antibody; Solute carrier family 33 (acetyl CoA transporter) member 1 antibody; Solute carrier family 33 member 1 antibody; spastic paraplegia 42 (autosomal dominant) antibody; SPG42 antibody
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											宿主:Rabbit
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											反應(yīng)種屬:Human,Mouse,Rat
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											免疫原:Synthetic peptide of Human SLC33A1
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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:Antigen affinity purification
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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:-20°C, pH7.4 PBS, 0.05% NaN3, 40% Glycerol
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											產(chǎn)品提供形式:Liquid
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											應(yīng)用范圍:ELISA,WB
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											推薦稀釋比:Application Recommended Dilution ELISA 1:2000-1:5000 WB 1:500-1:2000 
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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:Probable acetyl-CoA transporter necessary for O-acetylation of gangliosides. Negatively regulates BMP signaling.
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											基因功能參考文獻:- results indicate that increased expression of AT-1 can cause an autistic-like phenotype by affecting key neuronal metabolic pathways. PMID: 27242167
- SLC33A1 can negatively regulate BMP signaling. PMID: 25402622
- Homozygosity mapping displayed a region of commonality among three families at chromosome 3q25. Deep sequencing and conventional sequencing disclosed homozygous or compound heterozygous mutations for all affected subjects in SLC33A1. PMID: 22243965
- translocates acetyl-CoA into the ER lumen and is essential for cell viability PMID: 20826464
- A missense mutation in SLC33A1 causes autosomal-dominant spastic paraplegia. PMID: 19061983
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											相關(guān)疾?。?/div>Spastic paraplegia 42, autosomal dominant (SPG42); Congenital cataracts, hearing loss, and neurodegeneration (CCHLND)亞細胞定位:Endoplasmic reticulum membrane; Multi-pass membrane protein.蛋白家族:SLC33A transporter family組織特異性:Ubiquitous. Detected in heart, brain, placenta, lung, liver, skeletal muscle, kidney and pancreas. With strongest signals in pancreas.數(shù)據(jù)庫鏈接:
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