Recombinant Human Hsp60 Protein

Carrier Free

Azide Free

≥95%(SDS-PAGE)

功能和特点

表达系统: E. coli
Accession #: P10809
蛋白标签: N-His

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货号 (SKU)	包装规格	是否现货
rp169616-10μg (试用装) 申请此免费试用装（?）作为尊贵的客户，您每年可免费申请一次试用装产品，尽享探索与享受！	10μg	现货
rp169616-100μg	100μg	现货
rp169616-1mg	1mg	现货

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点击查看蛋白信息: HSPD1

Accession#:P10809 (3) Gene ID:3329 (3) Hsp60 (3) HSPD1 (3)

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基本描述

产品名称	Recombinant Human Hsp60 Protein
别名	重组人Hsp60蛋白 \| 人热休克蛋白60重组蛋白
英文别名	60 kDa chaperonin \| Chaperonin 60 \| CPN60 \| EC 5.6.1.7 \| Heat shock protein 60 \| Hsp60 \| HSP-60 \| HuCHA60 \| Mitochondrial matrix protein P1 \| P60 lymphocyte protein \| 60 kDa chaperonin \| Chaperonin 60 (CPN60) \| Heat shock protein 60 (HSP-60 \| Hsp60) \| HuC
规格或纯度	Carrier Free, Azide Free, ≥95%(SDS-PAGE)
产品介绍	Purity:>95%, by SDS-PAGE visualized with Coomassie® Blue Staining. Description： HSPD1, also known as HSP60, is a member of the chaperonin family. HSPD1 may function as a signaling molecule in the innate immune system. This protein is essential for the folding and assembly of newly imported proteins in the mitochondria. It may also prevent misfolding and promote the refolding and proper assembly of unfolded polypeptides generated under stress conditions in the mitochondrial matrix. HSPD1 gene is adjacent to a related family member and the region between the 2 genes functions as a bidirectional promoter. Several pseudogenes have been associated with this gene. Mutations associated with this gene cause autosomal recessive spastic paraplegia 13. Defects in HSPD1 are a cause of spastic paraplegia autosomal dominant type 13 (SPG13). Spastic paraplegia is a degenerative spinal cord disorder characterized by a slow, gradual, progressive weakness and spasticity of the lower limbs. Defects in HSPD1 are the cause of leukodystrophy hypomyelinating type 4 (HLD4); also called mitochondrial HSP60 chaperonopathy or MitCHAP-60 disease. HLD4 is a severe autosomal recessive hypomyelinating leukodystrophy. HSPD1 is clinically characterized by infantile-onset rotary nystagmus, progressive spastic paraplegia, neurologic regression, motor impairment, profound mental retardation. Death usually occurs within the first two decades of life.
表达系统	E. coli
氨基酸	1-573 aa
纯度	>95% (SDS-PAGE)
蛋白标签	N-His
无载体	Yes
无动物源	No
Accession #	P10809
来源	Recombinant
预测分子量	63.2 kDa
SDS-PAGE	62.0 kDa, under reducing conditions.

图片

SDS-PAGE: Recombinant Human Hsp60 Protein (rp169616)

Recombinant Human Hsp60 Protein (rp169616) - SDS-PAGE
3 μg/lane of Recombinant Human Hsp60 Protein was resolved with SDS-PAGE under reducing (R) and visualized by Coomassie® Blue staining, showing a band at 62.0 kDa under reducing conditions.

产品规格参数

物理外观	Lyophilized
储存缓冲液	Lyophilized form PBS, 8% Trahalose, pH7.4
复溶	We recommend that this vial be briefly centrifuged prior to opening to bring the contents to the bottom. Reconstitute at 0.5 mg/mL in sterile distilled water. Stock solutions should be apportioned into working aliquots and stored at ≤ -20 °C. Further dilutions should be made in appropriate buffered solutions.
储存温度	-20°C储存,避免反复冻融
运输条件	超低温冰袋运输
稳定性与储存	Store at -20°C for 1 year, store at 2-8℃ for 1 month. Avoid freeze / thaw cycle.

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找到2个结果

批号(Lot Number)	证书类型	日期	货号
ZJ24F0102577	分析证书	24-01-30	rp169616
ZJ24F0102576	分析证书	24-01-30	rp169616

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Recombinant Human Hsp60 Protein

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