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Apolipoprotein L/APOL1 Protein, Human, Recombinant (His)

Apolipoprotein L/APOL1 Protein, Human, Recombinant (His)

产品编号 TMPY-02956
别名: APOL1, apolipoprotein L1, APOL, FSGS4, APOL-I, APO-L

APOL1, also known as apolipoprotein L1, is a minor apoprotein component of HDL (High-density lipoprotein) or 'good cholesterol' which is synthesized in the liver and also in many other tissues, including pancreas, kidney, and brain. APOL1 belongs to the apolipoprotein L family. It may play a role in lipid exchange and transport throughout the body. It may also participate in reverse cholesterol transport from peripheral cells to the liver. Defects in APOL1 are the cause of focal segmental glomerulosclerosis type 4 (FSGS4). It is a renal pathology defined by the presence of segmental sclerosis in glomeruli and resulting in proteinuria, reduced glomerular filtration rate and edema. Renal insufficiency often progresses to end-stage renal disease, a highly morbid state requiring either dialysis therapy or kidney transplantation.

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Apolipoprotein L/APOL1 Protein, Human, Recombinant (His)
规格 价格/CNY 货期 数量
50 μg ¥ 3,820 现货
100 μg ¥ 6,530 5日内发货
200 μg ¥ 11,130 5日内发货
500 μg ¥ 22,510 5日内发货
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产品目录号及名称: Apolipoprotein L/APOL1 Protein, Human, Recombinant (His) (TMPY-02956)
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产品描述 APOL1, also known as apolipoprotein L1, is a minor apoprotein component of HDL (High-density lipoprotein) or 'good cholesterol' which is synthesized in the liver and also in many other tissues, including pancreas, kidney, and brain. APOL1 belongs to the apolipoprotein L family. It may play a role in lipid exchange and transport throughout the body. It may also participate in reverse cholesterol transport from peripheral cells to the liver. Defects in APOL1 are the cause of focal segmental glomerulosclerosis type 4 (FSGS4). It is a renal pathology defined by the presence of segmental sclerosis in glomeruli and resulting in proteinuria, reduced glomerular filtration rate and edema. Renal insufficiency often progresses to end-stage renal disease, a highly morbid state requiring either dialysis therapy or kidney transplantation.
种属 Human
表达系统 Baculovirus-Insect Cells
标签 His
蛋白编号 Q2KHQ6
别名 APOL1, apolipoprotein L1, APOL, FSGS4, APOL-I, APO-L
蛋白构建 A DNA sequence encoding the human APOL1 (Q2KHQ6) (Met1-Leu398) was expressed with a C-terminal polyhistidine tag.
蛋白纯度 ≥ 80 % as determined by SDS-PAGE. ≥ 90 % as determined by SEC-HPLC.

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分子量 Approxiamtely 42.53 kDa
内毒素 < 1.0 EU per μg of the protein as determined by the LAL method.
缓冲液 Lyophilized from sterile 20mM Tris, 300mM NaCl, 10% glycerol, 0. 5mM TCEP, pH 7.5. Please contact us for any concerns or special requirements. Normally 5 % - 8 % trehalose, mannitol and 0. 01% Tween 80 are added as protectants before lyophilization. Please refer to the specific buffer information in the hard copy of CoA.
复溶方法 A hardcopy of datasheet with reconstitution instructions is sent along with the products. Please refer to it for detailed information.
存储

Samples are stable for up to twelve months from date of receipt at -20℃ to -80℃. Store it under sterile conditions at -20℃ to -80℃. It is recommended that the protein be aliquoted for optimal storage. Avoid repeated freeze-thaw cycles.

运输方式

In general, recombinant proteins are provided as lyophilized powder which are shipped at ambient temperature.Bulk packages of recombinant proteins are provided as frozen liquid. They are shipped out with blue ice unless customers require otherwise.

研究背景 APOL1, also known as apolipoprotein L1, is a minor apoprotein component of HDL (High-density lipoprotein) or 'good cholesterol' which is synthesized in the liver and also in many other tissues, including pancreas, kidney, and brain. APOL1 belongs to the apolipoprotein L family. It may play a role in lipid exchange and transport throughout the body. It may also participate in reverse cholesterol transport from peripheral cells to the liver. Defects in APOL1 are the cause of focal segmental glomerulosclerosis type 4 (FSGS4). It is a renal pathology defined by the presence of segmental sclerosis in glomeruli and resulting in proteinuria, reduced glomerular filtration rate and edema. Renal insufficiency often progresses to end-stage renal disease, a highly morbid state requiring either dialysis therapy or kidney transplantation.

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Keywords

Apolipoprotein L/APOL1 Protein, Human, Recombinant (His) APOL 1 FSGS 4 APOL-1 APOL1 FSGS-4 apolipoprotein L1 APOL FSGS4 APOL-I APO-L recombinant recombinant-proteins proteins protein

 

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