GTX03806
LONP1 antibody
Cannot supply to this region.
- SKU:
- GTX03806
- Additional Names:
- lon peptidase 1, mitochondrial , CODASS , LON , LONP , LonHS , PIM1 , PRSS15 , hLON
- Application:
- ELISA, Flow Cytometry, WB, IHC-P, IF, ICC
- Concentration:
- 0.5 mg/ml
- Physical State:
- Liquid
- Species Reactivity:
- Human
- Purification:
- Affinity Purified
- Storage Conditions:
- -20[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., 2-8[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., -20[o]C/-70[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted.
- Supplier:
- Genetex
- Host:
- Rabbit
- Reactivities:
- Human, Mouse, Rat
- Buffer:
- 4mg Trehalose, 0.9mg NaCl, 0.2mg Na₂HPO₄, 0.05mg sodium azide.
- Immunogen:
- E.coli-derived human LONP1/Lon recombinant protein (Position: R137-A320).
- Uniprot:
- P36776
- Synonyms:
- CODASS;hLON;hLON ATP-dependent protease;LON;lon protease homolog, mitochondrial;Lon protease-like protein;LonHS;LONP;mitochondrial ATP-dependent protease Lon;mitochondrial lon protease-like protein;PIM1;PRSS15;serine protease 15
- Extra Details:
- This gene encodes a mitochondrial matrix protein that belongs to the Lon family of ATP-dependent proteases. This protein mediates the selective degradation of misfolded, unassembled or oxidatively damaged polypeptides in the mitochondrial matrix. It may also have a chaperone function in the assembly of inner membrane protein complexes, and participate in the regulation of mitochondrial gene expression and maintenance of the integrity of the mitochondrial genome. Decreased expression of this gene has been noted in a patient with hereditary spastic paraplegia (PMID:18378094). Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Feb 2013]
- Shipping Conditions:
- Blue Ice