GRHPR MaxPab mouse polyclonal antibody (B01P)
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More Files
- More Functions
Western Blot (Tissue lysate)
GRHPR MaxPab polyclonal antibody. Western Blot analysis of GRHPR expression in human liver.
Western Blot (Transfected lysate)
Western Blot analysis of GRHPR expression in transfected 293T cell line (H00009380-T01) by GRHPR MaxPab polyclonal antibody.
Lane 1: GRHPR transfected lysate(36.08 KDa).
Lane 2: Non-transfected lysate.
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Specification
Product Description
Mouse polyclonal antibody raised against a full-length human GRHPR protein.
Immunogen
GRHPR (NP_036335.1, 1 a.a. ~ 328 a.a) full-length human protein.
Sequence
MRPVRLMKVFVTRRIPAEGRVALARAADCEVEQWDSDEPIPAKELERGVAGAHGLLCLLSDHVDKRILDAAGANLKVISTMSVGIDHLALDEIKKRGIRVGYTPDVLTDTTAELAVSLLLTTCRRLPEAIEEVKNGGWTSWKPLWLCGYGLTQSTVGIIGLGRIGQAIARRLKPFGVQRFLYTGRQPRPEEAAEFQAEFVSTPELAAQSDFIVVACSLTPATEGLCNKDFFQKMKETAVFINISRGDVVNQDDLYQALASGKIAAAGLDVTSPEPLPTNHPLLTLKNCVILPHIGSATHRTRNTMSLLAANNLLAGLRGEPMPSELKL
Host
Mouse
Reactivity
Human
Interspecies Antigen Sequence
Mouse (85); Rat (85)
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 (Tissue lysate)
GRHPR MaxPab polyclonal antibody. Western Blot analysis of GRHPR expression in human liver.Western Blot (Transfected lysate)
Western Blot analysis of GRHPR expression in transfected 293T cell line (H00009380-T01) by GRHPR MaxPab polyclonal antibody.
Lane 1: GRHPR transfected lysate(36.08 KDa).
Lane 2: Non-transfected lysate.
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Gene Info — GRHPR
Entrez GeneID
9380GeneBank Accession#
NM_012203.1Protein Accession#
NP_036335.1Gene Name
GRHPR
Gene Alias
GLXR, GLYD, PH2
Gene Description
glyoxylate reductase/hydroxypyruvate reductase
Gene Ontology
HyperlinkGene Summary
This gene encodes an enzyme with hydroxypyruvate reductase, glyoxylate reductase, and D-glycerate dehydrogenase enzymatic activities. The enzyme has widespread tissue expression and has a role in metabolism. Type II hyperoxaluria is caused by mutations in this gene. [provided by RefSeq
Other Designations
OTTHUMP00000046131|glycerate-2-dehydrogenase
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Interactome
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Pathway
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Disease
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