Antibody data
- Antibody Data
- Antigen structure
- References [2]
- Comments [0]
- Validations
- Immunocytochemistry [1]
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Validation data
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- Product number
- AF852 - Provider product page
- Provider
- R&D Systems
- Product name
- Mouse CD30/TNFRSF8 Antibody
- Antibody type
- Polyclonal
- Description
- Antigen Affinity-purified. Detects CD30/TNFRSF8 in direct ELISAs and Western blots.
- Reactivity
- Mouse
- Host
- Goat
- Conjugate
- Unconjugated
- Antigen sequence
Q60846
- Isotype
- IgG
- Vial size
- 100 ug
- Concentration
- LYOPH
- Storage
- Use a manual defrost freezer and avoid repeated freeze-thaw cycles. 12 months from date of receipt, -20 to -70 °C as supplied. 1 month, 2 to 8 °C under sterile conditions after reconstitution. 6 months, -20 to -70 °C under sterile conditions after reconstitution.
Submitted references Lymphomagenesis, hydronephrosis, and autoantibodies result from dysregulation of IL-9 and are differentially dependent on Th2 cytokines.
Lymphomagenesis, hydronephrosis, and autoantibodies result from dysregulation of IL-9 and are differentially dependent on Th2 cytokines.
Lauder AJ, Jolin HE, Smith P, van den Berg JG, Jones A, Wisden W, Smith KG, Dasvarma A, Fallon PG, McKenzie AN
Journal of immunology (Baltimore, Md. : 1950) 2004 Jul 1;173(1):113-22
Journal of immunology (Baltimore, Md. : 1950) 2004 Jul 1;173(1):113-22
Lymphomagenesis, hydronephrosis, and autoantibodies result from dysregulation of IL-9 and are differentially dependent on Th2 cytokines.
Lauder AJ, Jolin HE, Smith P, van den Berg JG, Jones A, Wisden W, Smith KG, Dasvarma A, Fallon PG, McKenzie AN
Journal of immunology (Baltimore, Md. : 1950) 2004 Jul 1;173(1):113-22
Journal of immunology (Baltimore, Md. : 1950) 2004 Jul 1;173(1):113-22
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Supportive validation
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- R&D Systems (provider)
- Main image
- Experimental details
- CD30/TNFRSF8 in Mouse Splenocytes. CD30/TNFRSF8 was detected in immersion fixed mouse splenocytes using 15 µg/mL Goat Anti-Mouse CD30/TNFRSF8 Antigen Affinity-purified Polyclonal Antibody (Catalog # AF852) for 3 hours at room temperature. Cells were stained (red) and counterstained (green). View our protocol for Fluorescent ICC Staining of Non-adherent Cells.