AFG3L2 rabbit pAb - ES8866

AFG3L2 rabbit pAb

Sizes: 50μL, 100μL

Catalogue Numbers: ES8866-50, ES8866-100

Citations, Manuals and MSDS Available upon request.

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. [provided by RefSeq, Jul 2008],

Alternate Name: AFG3-like protein 2 (EC 3.4.24.-) (Paraplegin-like protein)

Source: Rabbit

Applications: WB; ELISA

Dilution: WB 1:500-2000, ELISA 1:10000-20000

Reactivity: Human; Rat; Mouse;

Immunogen: Synthesized peptide derived from human AFG3L2. at AA range: 744-793

Storage and Stability: -20°C/1 year

Clonality: Polyclonal

Isotype: IgG

Concentration: 1 mg/ml

Observed Band (KD): 88kD

Human Gene ID: 10939

Human SWISS Prot NO: Q9Y4W6

Subcellular Location: Mitochondrion. Mitochondrion inner membrane; Multi-pass membrane protein.

Research Use Only