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FTL (基因名), Ferritin light chain (蛋白名), fril_human.
产品名称:

Human FTL/ Ferritin light chain Recombinant Protein
铁蛋白轻链

货号:

R1905h

商标:
EIAab®
监管等级:
别名:

Ferritin L subunit

序列号:
P02792
来源:
E.coli
种属:
Human
标签:
His
序列:
57-175aa
预估分子量:
13.09 kDa (monomer)
纯度:
Greater than 95% by SDS-PAGE
浓度:
Reconstitution Dependent
形态:
Liquid
内毒素水平:
Please contact protein@eiaab.com The technician for more information.
应用:
存储缓冲液:
50mM NaH2PO4, 500mM NaCl Buffer with 500mM Imidazole, 10%glycerol(PH8.0)
存储:
Store at -20°C. (Avoid repeated freezing and thawing.)
研究领域:
Neurosciences
Human FTL Protein
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Human FTL Protein
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产品说明书
数据表: 下载说明书
MSDS: MSDS
在线询价


R&D 技术数据
Human FTL Protein
Recombinant human FTL protein was determined by 12% SDS-PAGE stained with Coomassie Blue under reducing conditions.
基因位点
Cytogenetic band: 19q13.33 by HGNC 19q13.33 by Entrez Gene 19q13.33 by Ensembl
FTL Gene in genomic location: bands according to Ensembl, locations according to GeneLoc (and/or Entrez Gene and/or Ensembl if different)
基因位点
通用注释


亚单元:
Oligomer of 24 subunits. There are two types of subunits: L (light) chain and H (heavy) chain. The major chain can be light or heavy, depending on the species and tissue type. The functional molecule forms a roughly spherical shell with a diameter of 12 nm and contains a central cavity into which the insoluble mineral iron core is deposited. Iron enters the spherical protein shell through pores that are formed between subunits. Mutations leading to truncation or the addition of extra residues at the C-terminus interfere with normal pore formation and with iron accumulation.


功能:
Stores iron in a soluble, non-toxic, readily available form. Important for iron homeostasis. Iron is taken up in the ferrous form and deposited as ferric hydroxides after oxidation. Also plays a role in delivery of iron to cells. Mediates iron uptake in capsule cells of the developing kidney.


亚细胞位置:
N/A


该产品尚未在任何出版物中被引用。

[1].
"A new missense mutation in the L ferritin coding sequence associated with elevated levels of glycosylated ferritin in serum and absence of iron overload."

[2].
"Structure of human ferritin L chain."

[3].
"Screening for mutations of the ferritin light and heavy genes in Parkinson's disease patients with hyperechogenicity of the substantia nigra."

[4].
"Genetic variation and antioxidant response gene expression in the bronchial airway epithelium of smokers at risk for lung cancer."

[5].
"Oxidative stress and cell death in cells expressing L-ferritin variants causing neuroferritinopathy."

[6].
"Mutant ferritin L-chains that cause neurodegeneration act in a dominant-negative manner to reduce ferritin iron incorporation."

[7].
"Unraveling of the E-helices and disruption of 4-fold pores are associated with iron mishandling in a mutant ferritin causing neurodegeneration."

[8].
"Bilateral cataract in a subject carrying a C to A transition in the L ferritin promoter region."

[9].
"Identification of L-ferritin in neuromelanin granules of the human substantia nigra: a targeted proteomics approach."

[10].
"HFE, SLC40A1, HAMP, HJV, TFR2, and FTL mutations detected by denaturing high-performance liquid chromatography after iron phenotyping and HFE C282Y and H63D genotyping in 785 HEIRS Study participants."
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