MIPEP polyclonal antibody
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More Files
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Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
Immunohistochemical staining of human duodenum with MIPEP polyclonal antibody (Cat # PAB22575) strong cytoplasmic positivity in glandular cells.
Immunofluorescence
Immunofluorescent staining of human cell line U-251 MG with MIPEP polyclonal antibody (Cat # PAB22575) at 1-4 ug/mL dilution shows positivity in mitochondria.
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Specification
Product Description
Rabbit polyclonal antibody raised against recombinant MIPEP.
Immunogen
Recombinant protein corresponding to amino acids of human MIPEP.
Sequence
SMLGRTRYQHVTGTRCPTDFAEVPSILMEYFANDYRVVNQFARHYQTGQPLPKNMVSRLCESKKVCAAADMQLQVFYATLDQIYH
Host
Rabbit
Reactivity
Human
Form
Liquid
Purification
Antigen affinity purification
Isotype
IgG
Recommend Usage
Immunofluorescence (1-4 ug/mL)
The optimal working dilution should be determined by the end user.Storage Buffer
In PBS, pH 7.2 (40% glycerol, 0.02% sodium azide)
Storage Instruction
Store at 4°C. For long term storage store at -20°C.
Aliquot to avoid repeated freezing and thawing.Note
This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Applications
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
Immunohistochemical staining of human duodenum with MIPEP polyclonal antibody (Cat # PAB22575) strong cytoplasmic positivity in glandular cells.Immunofluorescence
Immunofluorescent staining of human cell line U-251 MG with MIPEP polyclonal antibody (Cat # PAB22575) at 1-4 ug/mL dilution shows positivity in mitochondria. -
Gene Info — MIPEP
Entrez GeneID
4285Protein Accession#
Q99797Gene Name
MIPEP
Gene Alias
HMIP, MIP
Gene Description
mitochondrial intermediate peptidase
Omim ID
602241Gene Ontology
HyperlinkGene Summary
The product of this gene performs the final step in processing a specific class of nuclear-encoded proteins targeted to the mitochondrial matrix or inner membrane. This protein is primarily involved in the maturation of oxidative phosphorylation (OXPHOS)-related proteins. This gene may contribute to the functional effects of frataxin deficiency and the clinical manifestations of Friedreich ataxia. [provided by RefSeq
Other Designations
OTTHUMP00000018121|OTTHUMP00000042292
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