SQRDL purified MaxPab mouse polyclonal antibody (B01P)
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More Files
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Specifications
Product Description
Mouse polyclonal antibody raised against a full-length human SQRDL protein.
Immunogen
SQRDL (NP_067022.1, 1 a.a. ~ 450 a.a) full-length human protein.
Sequence
MVPLVAVVSGPRAQLFACLLRLGTQQVGPLQLHTGASHAARNHYEVLVLGGGSGGITMAARMKRKVGAENVAIVEPSERHFYQPIWTLVGAGAKQLSSSGRPTASVIPSGVEWIKARVTELNPDKNCIHTDDDEKISYRYLIIALGIQLDYEKIKGLPEGFAHPKIGSNYSVKTVEKTWKALQDFKEGNAIFTFPNTPVKCAGAPQKIMYLSEAYFRKTGKRSKANIIFNTSLGAIFGVKKYADALQEIIQERNLTVNYKKNLIEVRADKQEAVFENLDKPGETQVISYEMLHVTPPMSPPDVLKTSPVADAAGWVDVDKETLQHRRYPNVFGIGDCTNLPTSKTAAAVAAQSGILDRTISVIMKNQTPTKKYDGYTSCPLVTGYNRVILAEFDYKAEPLETFPFDQSKERLSMYLMKADLMPFLYWNMMLRGYWGGPAFLRKLFHLGMS
Host
Mouse
Reactivity
Human
Interspecies Antigen Sequence
Mouse (86); Rat (89)
Quality Control Testing
Antibody reactive against mammalian transfected lysate.
Storage Buffer
In 1x PBS, pH 7.4
Storage Instruction
Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.
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Applications
Western Blot (Transfected lysate)
Western Blot analysis of SQRDL expression in transfected 293T cell line by SQRDL MaxPab polyclonal antibody.
Lane 1: SQRDL transfected lysate(49.5 KDa).
Lane 2: Non-transfected lysate.
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Gene Info — SQRDL
Entrez GeneID
58472GeneBank Accession#
NM_021199Protein Accession#
NP_067022.1Gene Name
SQRDL
Gene Alias
CGI-44
Gene Description
sulfide quinone reductase-like (yeast)
Gene Ontology
HyperlinkOther Designations
sulfide dehydrogenase like
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Interactomes
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Publication Reference
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Loss of the mitochondrial i-AAA protease YME1L leads to ocular dysfunction and spinal axonopathy.
Sprenger HG, Wani G, Hesseling A, König T, Patron M, MacVicar T, Ahola S, Wai T, Barth E, Rugarli EI, Bergami M, Langer T.
EMBO Molecular Medicine 2018 Nov; [Epub].
Application:WB-Ti, Mouse, Forebrain, Cerebellar, Spinal cord.
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Loss of the mitochondrial i-AAA protease YME1L leads to ocular dysfunction and spinal axonopathy.
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