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AFG3L2 Mouse anti-Human, Clone: OTI2D3, lyophilized, TrueMAB™
SDP

Catalog No. 501662866
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100 μg
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Catalog No. Quantity
50-166-2866 100 μg
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Catalog No. 50-166-2866 Supplier OriGene Supplier No. CF504404
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Mouse Monoclonal Antibody

Reconstitute with PBS (pH 7.3) and recommend to perform another round of desalting process using Product No. 7KMWCO

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 AFG3L2
Applications Western Blot
Classification Monoclonal
Clone OTI2D3
Conjugate Unconjugated
Formulation PBS with 8% trehalose and no preservative; pH 7.3
Gene AFG3L2
Gene Accession No. Q9Y4W6
Gene Alias SCA28, SPAX5
Gene Symbols AFG3L2
Host Species Mouse
Immunogen Human recombit protein fragment corresponding to amino acids 1-250 of human AFG3L2 produced in E.coli.
Purification Method Affinity Chromatography
Quantity 100 μg
Regulatory Status RUO
Primary or Secondary Primary
Gene ID (Entrez) 10939
Target Species Human
Content And Storage -20° C, Avoid Freeze/Thaw Cycles
Product Type Antibody
Form Lyophilized
Isotype IgG1
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