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Rabbit Anti-PMPCA Antibody (CSB-PA606021ESR1HU)
Supplier: CUSABIO BIOTECH CO.
Mitochondrial-processing peptidase subunit alpha Antibody,Alpha-MPP Antibody,P-55 Antibody,PMPCA Antibody,INPP5E Antibody,KIAA0123 Antibody,MPPA AntibodyMore alternative names for the antibody
1200002L24Rik antibody|4933435E07Rik antibody|Alpha MPP antibody|Alpha-MPP antibody|FLJ26258 antibody|Inositol polyphosphate 5 phosphatase, 72 kD antibody|INPP5E antibody|KIAA0123 antibody|MGC104197 antibody|MGC93916 antibody|Mitochondrial matrix processing protease, alpha subunit antibody|mitochondrial processing peptidase subunit alpha antibody|Mitochondrial-processing peptidase subunit alpha antibody|MPPA_HUMAN antibody|P 55 antibody|P-55 antibody|Peptidase (mitochondrial processing) alpha antibody|pmpca antibody|RP11-413M3.1 antibody|RP23-306D20.8 antibody
Anti-PMPCA antibody (ab140171)
Anti-PMPCA antibody (ab140171)
Recommended applications: ELISA, IHC
Recommended dilution: Recommended dilution:IHC:1:20-1:200
Recommended protocols: check protocols
|Catalogue No.|| |
Recombinant human Mitochondrial-processing peptidase subunit alpha protein (456-525AA)
|Recommended dilution|| |
|Molecular weight|| |
Antigen Affinity Purified
Shipped at 4 Celcius Degree. Upon delivery aliquot and store at -20 Celcius Degree or -80 Celcius Degree. Avoid repeated freeze.
|Database links|| |
Entrez Gene:480677( Dog), Entrez Gene:23203( Human), Entrez Gene:66865( Mouse), Entrez Gene:296588( Rat), Omim:613036( Human), SwissProt:Q10713( Human), SwissProt:Q9DC61( Mouse), SwissProt:P20069( Rat), Unigene:495471( Human), Unigene:250359( Mouse), Unigene:11175( Rat)
|Protein function|| |
Cleaves presequences (transit peptides) from mitochondrial protein precursors. .
|Protein tissue specificity|| |
Ubiquitously expressed with highest expression in fetal tissues and adult brain, cerebellum and cerebellar vermis. .
|Involvement in disease|| |
Spinocerebellar ataxia, autosomal recessive, 2 (SCAR2) [MIM:213200]: A form of spinocerebellar ataxia, a clinically and genetically heterogeneous group of cerebellar disorders due to degeneration of the cerebellum with variable involvement of the brainstem and spinal cord. SCAR2 is characterized by onset of impaired motor development and ataxic gait in early childhood. Additional features often include loss of fine motor skills, dysarthria, nystagmus, cerebellar signs, and delayed cognitive development with intellectual disability. . Note=The disease is caused by mutations affecting the gene represented in this entry.
|Protein sequence and domain|| |
Belongs to the peptidase M16 family.
|Protein cellular localization|| |
Mitochondrion matrix . Mitochondrion inner membrane .
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CUSABIO BIOTECH CO.
|Product type|| |
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