AFG3L2 polyclonal (N-term), anti-human

Background:
This gene encodes a protein localized in mitochondria and closely related to paraplegin. The paraplegin gene is responsible for an autosomal recessive form of hereditary spastic paraplegia. This gene is a candidate gene for other hereditary spastic paraplegias or neurodegenerative disorders.

Other Names:
AFG3-like protein 2, 3424-, Paraplegin-like protein, AFG3L2

Target/Specificity:
This AFG3L2 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 52-80 amino acids from the N-terminal region of human AFG3L2.

Antigen Region:
52-80

Antigen Type: Synthetic Peptide

Gene Name: AFG3L2 {ECO:0000303|PubMed:10395799, ECO:0000312|HGNC:HGNC:315}
Gene ID: 10939
Primary Accession: Q9Y4W6
NCBI Accession: NP_006787.2
Other Accession: Q8JZQ2; Q2KJI7; NP_006787.2
Format: Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein A column, followed by peptide affinity purification.