Rabbit Polyclonal Antibody to SLC25A17 (N-term)
货号:
P30466
别名:
Peroxisomal membrane protein PMP34, 34 kDa peroxisomal membrane protein, Solute carrier family 25 member 17, SLC25A17, PMP34
应用:
WB,FCM
反应种属:
Human, Mouse
抗体类型:
Primary antibody
Swissprot:
O43808
规格:
目录价
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Description |
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This protein encodes a selenoprotein, which contains a selenocysteine (Sec) residue at its active site. The selenocysteine is encoded by the UGA codon that normally signals translation termination. The 3' UTR of selenoprotein genes have a common stem-loop structure, the sec insertion sequence (SECIS), that is necessary for the recognition of UGA as a Sec codon rather than as a stop signal. Studies suggest that this protein may regulate cytokine production, and thus play a key role in the control of the inflammatory response. |
Specification |
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Aliases | Peroxisomal membrane protein PMP34, 34 kDa peroxisomal membrane protein, Solute carrier family 25 member 17, SLC25A17, PMP34 |
Entrez GeneID | 10478 |
Swissprot | O43808 |
WB Predicted band size | 34.6kDa |
Host/Isotype | Rabbit IgG |
Antibody Type | Primary antibody |
Storage | Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles. |
Species Reactivity | Human, Mouse |
Immunogen | This SLC25A17 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 17-44 amino acids from the N-terminal region of human SLC25A17. |
Formulation | Purified antibody in PBS with 0.05% sodium azide. |
Application |
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WB | 1/1000 |
FCM | 1/10-1/50 |
Product Image
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Western blot analysis of SLC25A17 Antibody (N-term) (Cat. #P30466) in NCI-H460 cell line lysates (35ug/lane). SLC25A17 (arrow) was detected using the purified Pab.
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Western blot analysis of SLC25A17 Antibody (N-term) (Cat. #P30466) in Mouse NIH-3T3 cell line lysates (35ug/lane). SLC25A17 (arrow) was detected using the purified Pab.
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SLC25A17 Antibody (N-term) (Cat. #P30466) flow cytometry analysis of NCI-H460 cells (bottom histogram) compared to a negative control cell (top histogram).FITC-conjugated goat-anti-rabbit secondary antibodies were used for the analysis.