A24606
PMPCA Rabbit monoclonal antibody
Size
POA
- SKU:
- A24606
- Additional Names:
- Alpha-MPP|CLA1|CPD3|INPP5E|MAS2|P-55|PMPCA|SCAR2
- Application:
- ELISA, WB, IHC-P, IF, ICC, IP
- Molecular Weight:
- 58 kDa
- Species Reactivity:
- Human
- Purification:
- Affinity Purified
- Storage Conditions:
- -20[o]C Avoid freeze/thaw cycles.
- Supplier:
- Abclonal
- Host:
- Rabbit
- Reactivities:
- Human, Mouse, Rat
- Immunogen:
- Recombinant protein (or fragment).This information is considered to be commercially sensitive.
- Formulation:
- Unmodified
- Sequence:
- AQYTGGIAKLERDMSNVSLGPTPIPELTHIMVGLESCSFLEEDFIPFAVLNMMMGGGGSFSAGGPGKGMFSRLYLNVLNRHHWMYNATSYHHSYEDTGLLCIHASADPRQVREMVEIITKEFILMGGTVDTVELERAKTQLTSMLMMNLESRPVIFEDVGRQVLATRSRKLPHELCTLIRNVKPEDVKRVASKMLRGKPAVAALGDLTDLPTYEHIQTALSSKDGRLPRTYRLFR
- Uniprot:
- Q10713
- Synonyms:
- Alpha-MPP;cerebellar ataxia 1 (autosomal recessive);Cerebellar ataxia-1;CLA1;CPD3;inactive zinc metalloprotease alpha;inositol polyphosphate-5-phosphatase, 72 kD;INPP5E;MAS2;mitochondrial matrix processing protease, alpha subunit;mitochondrial-processing peptidase subunit alpha;P-55;peptidase, mitochondrial processing alpha subunit;SCAR2
- Extra Details:
- The protein encoded by this gene is found in the mitochondrion, where it represents the alpha subunit of a proteolytic heterodimer. This heterodimer is responsible for cleaving the transit peptide from nuclear-encoded mitochondrial proteins. Defects in this gene are a cause of spinocerebellar ataxia, autosomal recessive 2.
- Shipping Conditions:
- Blue Ice