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Elongation of very long chain fatty acids protein 4 (Elovl4), Recombinant Prote

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產(chǎn)品名稱: Elongation of very long chain fatty acids protein 4 (Elovl4), Recombinant Prote
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Elongation of very long chain fatty acids protein 4 (Elovl4), Recombinant Protein


Elongation of very long chain fatty acids protein 4 (Elovl4), Recombinant Prote  的詳細(xì)介紹
Product Name

Elongation of very long chain fatty acids protein 4 (Elovl4), Recombinant Protein

Full Product Name

Recombinant Mouse Elongation of very long chain fatty acids protein 4 (Elovl4)

Product Gene Name

Elovl4 recombinant protein

[Similar Products]
Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
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Sequence Positions
1-312aa; full length protein
Sequence
MGLLDSEPGS VLNAMSTAFN DTVEFYRWTW TIADKRVADW PLMQSPWPTI SISTLYLLFV WLGPKWMKDR EPFQMRLVLI IYNFGMVLLN LFIFRELFMG SYNAGYSYIC QSVDYSNDVN EVRIAGALWW YFVSKGVEYL DTVFFILRKK NNQVSFLHVY HHCTMFTLWW IGIKWVAGGQ AFFGAQMNSF IHVIMYSYYG LTAFGPWIQK YLWWKRYLTM LQLVQFHVTI GHTALSLYTD CPFPKWMHWA LIAYAISFIF LFLNFYTRTY NEPKQSKTGK TATNGISSNG VNKSEKALEN GKPQKNGKPK GE
3D Structure
ModBase 3D Structure for Q9EQC4
Host
Cell Free Expression
Form/Format
Liquid containing glycerol
Species
Mouse
Storage Buffer
Tris-based buffer, 50% glycerol.
Preparation and Storage
Store at -20 degree C, for extended storage, conserve at -20 degree C or -80 degree C.
Repeated freezing and thawing is not recommended. Store working aliquots at 4 degree C for up to one week.
ISO Certification
Manufactured in an ISO 13485:2003 and EN ISO 13485:2012 Certified Laboratory.
Other Notes
Small volumes of Elovl4 recombinant protein vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.
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Product Categories/Family for Elovl4 recombinant protein
Transmembrane Protein
Application Notes for Elovl4 recombinant protein
This is a recombinant transmembrane protein expressed in a cell-free expression system.
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NCBI/Uniprot data below describe general gene information for Elovl4. It may not necessarily be applicable to this product.
NCBI GI #
225543343
NCBI GeneID
83603
NCBI Accession #
NP_683743.2 [Other Products]
NCBI GenBank Nucleotide #
NM_148941.2 [Other Products]
UniProt Primary Accession #
Q9EQC4 [Other Products]
UniProt Secondary Accession #
Q8JZV3[Other Products]
UniProt Related Accession #
Q9EQC4[Other Products]
Molecular Weight
36,506 Da
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NCBI Official Full Name
elongation of very long chain fatty acids protein 4
NCBI Official Synonym Full Names
elongation of very long chain fatty acids (FEN1/Elo2, SUR4/Elo3, yeast)-like 4
NCBI Official Symbol
Elovl4??[Similar Products]
NCBI Protein Information
elongation of very long chain fatty acids protein 4
UniProt Protein Name
Elongation of very long chain fatty acids protein 4
UniProt Synonym Protein Names
3-keto acyl-CoA synthase Elovl4
Protein Family
Elongation of very long chain fatty acids protein
UniProt Gene Name
Elovl4??[Similar Products]
UniProt Synonym Gene Names
ELOVL FA elongase 4??[Similar Products]
UniProt Entry Name
ELOV4_MOUSE
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UniProt Comments for Elovl4
ELOVL4: Condensing enzyme that elongates saturated and monounsaturated very long chain fatty acids (VLCFAs). Elongates C24:0 and C26:0 acyl-CoAs. Seems to represent a photoreceptor- specific component of the fatty acid elongation system residing on the endoplasmic reticulum. May be implicated in docosahexaenoic acid (DHA) biosynthesis, which requires dietary consumption of the essential alpha-linolenic acid and a subsequent series of three elongation steps. May play a critical role in early brain and skin development. Defects in ELOVL4 are the cause of Stargardt disease type 3 (STGD3). STGD is one of the most frequent causes of macular degeneration in childhood. It is characterized by macular dystrophy with juvenile-onset, rapidly progressive course, alterations of the peripheral retina, and subretinal deposition of lipofuscin-like material. STGD3 inheritance is autosomal dominant. Defects in ELOVL4 are the cause of ichthyosis, spastic quadriplegia, and mental retardation (ISQMR). A severe autosomal recessive disorder characterized by ichthyosis apparent from birth, profound psychomotor retardation with essentially no development, spastic quadriplegia, and seizures. Belongs to the ELO family.

Protein type: Membrane protein, multi-pass; Cancer Testis Antigen (CTA); Membrane protein, integral; Endoplasmic reticulum; EC 2.3.1.199

Cellular Component: endoplasmic reticulum; integral to endoplasmic reticulum membrane; integral to membrane; membrane

Molecular Function: fatty acid elongase activity; transferase activity

Biological Process: fatty acid biosynthetic process; fatty acid elongation, saturated fatty acid; fatty acid metabolic process; lipid metabolic process; very-long-chain fatty acid biosynthetic process

Disease: Stargardt Disease 3
Research Articles on Elovl4
1. Studies indicate that Knock-IN and Knock-OUT strains of ELOVL4 (STGD3) model development has been to unveil the causal connection between the genotype and early-onset progressive cone degeneration in humans.
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Precautions
All of MyBioSource's Products are for scientific laboratory research purposes and are not for diagnostic, therapeutics, prophylactic or in vivo use. Through your purchase, you expressly represent and warrant to MyBioSource that you will properly test and use any Products purchased from MyBioSource in accordance with industry standards. MyBioSource and its authorized distributors reserve the right to refuse to process any order where we reasonably believe that the intended use will fall outside of our acceptable guidelines.
Disclaimer
While every efforts were made to ensure the accuracy of the information provided in this datasheet, MyBioSource will not be liable for any omissions or errors contained herein. MyBioSource reserves the right to make changes to this datasheet at any time without prior notice.

It is the responsibility of the customer to report product performance issues to MyBioSource within 30 days of receipt of the product. Please visit our Terms & Conditions page for more information.
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