Antibody data
- Antibody Data
- Antigen structure
- References [1]
- Comments [0]
- Validations
- Western blot [1]
- Immunohistochemistry [1]
- Other assay [1]
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Validation data
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- Product number
- PA5-24598 - Provider product page
- Provider
- Invitrogen Antibodies
- Product name
- IDO Polyclonal Antibody
- Antibody type
- Polyclonal
- Antigen
- Synthetic peptide
- Reactivity
- Human, Mouse
- Host
- Rabbit
- Vial size
- 400 µL
- Concentration
- 2 mg/mL
- Storage
- -20° C, Avoid Freeze/Thaw Cycles
Submitted references The extracts of Astragalus membranaceus enhance chemosensitivity and reduce tumor indoleamine 2, 3-dioxygenase expression.
Phacharapiyangkul N, Wu LH, Lee WY, Kuo YH, Wu YJ, Liou HP, Tsai YE, Lee CH
International journal of medical sciences 2019;16(8):1107-1115
International journal of medical sciences 2019;16(8):1107-1115
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Supportive validation
- Submitted by
- Invitrogen Antibodies (provider)
- Main image
- Experimental details
- Western blot analysis using an INDO polyclonal antibody (Product # PA5-24598) in mouse cerebellum tissue lysates (35 µg per lane).
Supportive validation
- Submitted by
- Invitrogen Antibodies (provider)
- Main image
- Experimental details
- Immunohistochemistry analysis in formalin-fixed, paraffin-embedded human lung carcinoma using an INDO polyclonal antibody (Product # PA5-24598), followed by HRP-conjugated secondary antibody and DAB staining.
Supportive validation
- Submitted by
- Invitrogen Antibodies (provider)
- Main image
- Experimental details
- Figure 4 The effects of PG2 on the expression and function of IDO. PG2 inhibited IDO protein expression in (A) B16F10 and (B) LL2 cells in a dose-dependent manner. After treatment with PG2 (0-100 ng/ml) for 24 h, the expression of IDO and TDO levels in B16F10 and LL2 cells were measured by Western blotting. The kynurenine assay was used for the kynurenine production in (C) B16F10 and (D) LL2 cells. The conditioned medium of (E) B16F10 and (F) LL2 after treated with indicated concentrations of PG2 for 24 h mixed with an equal amount of original medium. T cells were cultured in media conditioned from tumor cells for 72 h. The cell number were measured by staining with trypan blue. (n = 6, data are mean+- SD. * P < 0.05). PG2 induced Cx43 and inhibited IDO protein expression in (G) A549 and (H) PC9 cells in a dose-dependent manner. After treatment with PG2 (0-100 ng/ml) for 24 h, the expression of Cx43 and IDO levels in A549 and PC9 cells were measured by Western blotting.