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SCA28/AFG3L2 Rabbit anti-Human, Polyclonal, Bioss
SDP

Catalog No. 501981598
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50-198-1598 100 μL
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Catalog No. 50-198-1598 Supplier Bioss Supplier No. BS11704R
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Rabbit Polyclonal Antibody

AFG3L2 is a protein localized in mitochondria and closely related to paraplegin. The paraplegin gene is responsible for an autosomal recessive form of hereditary spastic paraplegia. AFG3L2 gene is a candidate gene for other hereditary spastic paraplegias or neurodegenerative disorders. 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.

Specifications

Antigen SCA28/AFG3L2
Applications Immunofluorescence, Immunohistochemistry (Paraffin), Western Blot
Classification Polyclonal
Concentration 1 μg/mL
Conjugate Unconjugated
Formulation PBS with 1% BSA, 50% glycerol and 0.09% sodium azide; pH
Gene AFG3L2
Gene Accession No. Q9Y4W6
Gene Alias 2310036I02Rik; AFG3 ATPase family gene 3-like 2; AFG3 ATPase family gene 3-like 2 (S. cerevisiae); AFG3 ATPase family member 3-like 2; AFG3 like AAA ATPase 2; AFG3 like matrix AAA peptidase subunit 2; AFG3(ATPase family gene 3)-like 2; Afg3l2; AFG3-like AAA ATPase 2; AFG3-like protein 2; AFG3-like protein 2 (Paraplegin-like protein); ATPase family gene 3, yeast; AW260507; BOS_22264; Emv66; FLJ25993; par; Paraplegin-like protein; SCA28; si:ch211-12e1.4; SPAX5
Gene Symbols AFG3L2
Host Species Rabbit
Immunogen KLH conjugated synthetic peptide derived from human AFG3L2.
Purification Method Protein A
Quantity 100 μL
Regulatory Status RUO
Primary or Secondary Primary
Gene ID (Entrez) 10939
Target Species Human
Content And Storage -20°C
Product Type Antibody
Form Liquid
Isotype IgG
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