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产品展示
Anti-ABCA1/ABC1/FITC,FITC标记的腺苷三磷酸结合盒转运体A1抗体
点击次数:270
价格:¥电议
更新日期:2026/8/7 18:57:00
生 产 地:中国大陆
产品型号:
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详细内容
产品名称:Anti-ABCA1/ABC1/FITC,FITC标记的腺苷三磷酸结合盒转运体A1抗体
中文名称:FITC标记的腺苷三磷酸结合盒转运体A1抗体
英文名称:Anti-ABCA1/ABC1/FITC
产品编号:BYK-1627R-FITC
产品别名:ATP binding cassette transporter A1; ABC 1; ABC Transporter 1; ABC1; ABCA 1; ABCA1; ATP binding Cassette 1; ATP binding cassette sub family A ABC1 member 1; ATP binding cassette sub family A member 1; ATP binding cassette sub-family A member 1; ATP binding Cassette Transporter 1; ATP-binding Cassette 1; ATP-binding Cassette Transporter 1; CERP; Cholesterol Efflux Regulatory Protein; FLJ14958; HDLDT1; Membrane bound; MGC164864; MGC165011; TD; TGD; ABCA1_HUMAN.
本公司另供应“FITC标记的腺苷三磷酸结合盒转运体A1抗体”的其他标记有:Alexa Fluor 350 Alexa Fluor 488 Alexa Fluor 555 Alexa Fluor 647 AP APC Biotin Cy3 Cy5 Cy5.5 Cy7 FITC Gold HRP PE PE-Cy3 PE-CY5 PE-CY5.5 PE-CY7 RBITC.
产品规格:100ug
产品浓度: 2mg/1ml
亚 型:IgG
纯化方法:affinity purified by Protein A
储 存 液:0.01M PBS, pH 7.4 with 10 mg/ml BSA and 0.1% Sodium azide
产品类型:标记一抗
抗体来源:Rabbit
克隆类型:polyclonal
保存条件:Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C.
Anti-ABCA1/ABC1/FITC,FITC标记的腺苷三磷酸结合盒转运体A1抗体技术说明,产品推荐,由于篇幅原因,更多信息请来电咨询:
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Anti-ABCA1/ABC1/FITC,FITC标记的腺苷三磷酸结合盒转运体A1抗体产品介绍:
The membrane-associated protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intracellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the ABC1 subfamily. Members of the ABC1 subfamily comprise the only major ABC subfamily found exclusively in multicellular eukaryotes. In humans, this protein functions as a cholesterol efflux pump in the cellular lipid removal pathway. Mutations in the human gene have been associated with Tangier's disease and familial high-density lipoprotein deficiency.


