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MOT1 Rabbit Polyclonal Antibody

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产品基本信息

产品货号
BD-PN0868
产品名称
MOT1 Rabbit Polyclonal Antibody
类别
常规抗体
基因名称
SLC16A1 MCT1
蛋白名称
Monocarboxylate transporter 1 (MCT 1) (Solute carrier family 16 member 1)
推荐应用
WB
反应种属
Human,Rat,Mouse
浓度
1 mg/ml
存储缓冲液
Liquid in PBS containing 50% glycerol, and 0.02% New type preservative N.
Human Gene ID
6566
Human Swissprot No.
P53985
Human Swissprot Link
https://www.uniprot.org/uniprotkb/P53985/entry
Mouse Swissprot No.
P53986
Mouse Swissprot Link
http://www.uniprot.org/uniprot/P53986
Rat Swissprot No.
P53987
Rat Swissprot Link
http://www.uniprot.org/uniprot/O54941P53987
免疫原
Synthesized peptide derived from human protein . at AA range: 240-320
特异性
MOT1 Polyclonal Antibody detects endogenous levels of protein.
稀释度
WB 1:500-2000 ELISA 1:5000-20000
预测分子量
55kD
运输及保存条件
-20°C/1 year
宿主
Polyclonal, Rabbit,IgG
背景介绍
The protein encoded by this gene is a proton-linked monocarboxylate transporter that catalyzes the movement of many monocarboxylates, such as lactate and pyruvate, across the plasma membrane. Mutations in this gene are associated with erythrocyte lactate transporter defect. Alternatively spliced transcript variants have been found for this gene.[provided by RefSeq, Oct 2009],
组织表达
Detected in heart and in blood lymphocytes and monocytes (at protein level). Widely expressed.
细胞定位
Cell membrane ; Multi-pass membrane protein .
功能
disease:Defects in SLC16A1 are the cause of familial hyperinsulinemic hypoglycemia type 7 (HHF7) [MIM:610021]; also known as exercise-induced hyperinsulinemic hypoglycemia. HHF7 is a dominantly inherited hypoglycemic disorder characterized by inappropriate insulin secretion during anaerobic exercise or on pyruvate load.,disease:Defects in SLC16A1 are the cause of symptomatic deficiency in lactate transport (SDLT) [MIM:245340]; also known as erythrocyte lactate transporter defect. Deficiency of lactate transporter may result in an acidic intracellular environment created by muscle activity with consequent degeneration of muscle and release of myoglobin and creatine kinase. This defect might compromise extreme performance in otherwise healthy individuals.,function:Proton-linked monocarboxylate transporter. Catalyzes the rapid transport across the plasma membrane of many monocarboxylates such as lactate, pyruvate, branched-chain oxo acids derived from leucine, valine and isoleucine, and the ketone bodies acetoacetate, beta-hydroxybutyrate and acetate.,similarity:Belongs to the major facilitator superfamily. Monocarboxylate porter (TC 2.A.1.13) family.,tissue specificity:Widely expressed in normal and in cancer cells.,
期货
现货
纯化
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

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