SPG7 Mouse Monoclonal Antibody (Biotin conjugated) [Clone ID: OTI3H10]

CAT#: TA800010AM

SPG7 mouse monoclonal antibody,clone 3H10, Biotinylated

Product Images

HEK293T cells were transfected with the pCMV6-ENTRY control (Left lane) or pCMV6-ENTRY SPG7 (RC206340, Right lane) cDNA for 48 hrs and lysed. Equivalent amounts of cell lysates (5 ug per lane) were separated by SDS-PAGE and immunoblotted with anti-SPG7. Positive lysates LY401085 (100ug) and LC401085 (20ug) can be purchased separately from OriGene.

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  Anti-SPG7 mouse monoclonal antibody (TA800010) immunofluorescent staining of COS7 cells transiently transfected by pCMV6-ENTRY SPG7 (RC206340).

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  Flow cytometric Analysis of Jurkat cells, using anti-SPG7 antibody (TA800010), (Red), compared to a nonspecific negative control antibody (TA50011), (Blue).

Specifications

Product Data

• Clone Name: OTI3H10
• Applications: FC, IF, WB
• Recommended Dilution: WB 1:2000, IF 1:100, FLOW 1:100
• Reactivities: Human, Mouse, Rat
• Host: Mouse
• Isotype: IgG1
• Clonality: Monoclonal
• Immunogen: Human recombinant protein fragment corresponding to amino acids 300-573 of human SPG7 (NP_003110) produced in E.coli.
• Formulation: PBS (pH 7.3) containing 1% BSA, 50% glycerol and 0.02% sodium azide.
• Concentration: 0.5 mg/ml
• Purification: Purified from mouse ascites fluids or tissue culture supernatant by affinity chromatography (protein A/G)
• Conjugation: Biotin
• Storage: Store at -20°C as received.
• Stability: Stable for 12 months from date of receipt.
• Predicted Protein Size: 88.1 kDa
• Gene Name: SPG7, paraplegin matrix AAA peptidase subunit
• Database Link:
  NP_003110
  Entrez Gene 234847 MouseEntrez Gene 353231 RatEntrez Gene 6687 Human
  UniProt ID Q9UQ90
• Background: This gene encodes a nuclear-encoded mitochondrial metalloprotease protein that is a member of the AAA (ATPases associated with a variety of cellular activities) protein family. Members of this protein family share an ATPase domain and have roles in diverse cellular processes including membrane trafficking, intracellular motility, organelle biogenesis, protein folding, and proteolysis. Two transcript variants encoding distinct isoforms have been identified for this gene. Mutations associated with this gene cause autosomal recessive spastic paraplegia 7. [provided by RefSeq, Jul 2008]
• Synonyms: CAR; CMAR; PGN; SPG5C

Reference Data

• Protein Families: Protease, Transmembrane