Recombinant Human FECH protein (ab158429)
- Datasheet
- References
- Protocols
Description
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Product name
Recombinant Human FECH protein -
Expression system
Wheat germ -
Protein length
Full length protein -
Animal free
No -
Nature
Recombinant -
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Species
Human -
Sequence
MRSLGANMAAALRAAGVLLRDPLASSSWRVCQPWRWKSGAAAAAVTTETA QHAQGAKPQVQPQKRKPKTGILMLNMGGPETLGDVHDFLLRLFLDQDLMT LPIQNKLAPFIAKRRTPKIQEQYRRIGGGSPIKIWTSKQGEGMVKLLDEL SPNTAPHKYYIGFRYVHPLTEEAIEEMERDGLERAIAFTQYPQYSCSTTG SSLNAIYRYYNQVGRKPTMKWSTIDRWPTHHLLIQCFADHILKELDHFPL EKRSEVVILFSAHSLPMSVVNRGDPYPQEVSATVQKVMERLEYCNPYRLV WQSKVGPMPWLGPQTDESIKGLCERGRKNILLVPIAFTSDHIETLYELDI EYSQVLAKECGVENIRRAESLNGNPLFSKALADLVHSHIQSNELCSKQLT LSCPLCVNPVCRETKSFFTSQQL -
Amino acids
1 to 423 -
Tags
GST tag N-Terminus
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Specifications
Our Abpromise guarantee covers the use of ab158429 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
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Applications
Western blot
ELISA
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Form
Liquid -
Additional notes
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Concentration information loading...
Preparation and Storage
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Stability and Storage
Shipped on dry ice. Upon delivery aliquot and store at -80ºC. Avoid freeze / thaw cycles.
pH: 8.00
Constituents: 0.31% Glutathione, 0.79% Tris HCl
General Info
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Alternative names
- EPP
- FCE
- Fch
see all -
Function
Catalyzes the ferrous insertion into protoporphyrin IX. -
Pathway
Porphyrin metabolism; protoheme biosynthesis; protoheme from protoporphyrin-IX: step 1/1. -
Involvement in disease
Erythropoietic protoporphyria (EPP) [MIM:177000]: A form of porphyria. Porphyrias are inherited defects in the biosynthesis of heme, resulting in the accumulation and increased excretion of porphyrins or porphyrin precursors. They are classified as erythropoietic or hepatic, depending on whether the enzyme deficiency occurs in red blood cells or in the liver. Erythropoietic protoporphyria is marked by excessive protoporphyrin in erythrocytes, plasma, liver and feces, and by widely varying photosensitive skin changes ranging from a burning or pruritic sensation to erythema, edema and wheals. Note=The disease is caused by mutations affecting the gene represented in this entry. -
Sequence similarities
Belongs to the ferrochelatase family. -
Cellular localization
Mitochondrion inner membrane. - Information by UniProt
Images
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SDS-PAGE - Recombinant Human FECH protein (ab158429)ab158429 on a 12.5% SDS-PAGE stained with Coomassie Blue.
Datasheets and documents
References
ab158429 has not yet been referenced specifically in any publications.
