Antibody data
- Antibody Data
- Antigen structure
- References [0]
- Comments [0]
- Validations
- Western blot [1]
- Immunocytochemistry [1]
Submit
Validation data
Reference
Comment
Report error
- Product number
- AF5737 - Provider product page
- Provider
- R&D Systems
- Product name
- Human SNF1LK2 Antibody
- Antibody type
- Polyclonal
- Description
- Immunogen affinity purified. Detects human SNF1LK2 in Western blots.
- Reactivity
- Human
- Host
- Goat
- Conjugate
- Unconjugated
- Antigen sequence
Q9H0K1
- 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.
No comments: Submit comment
Supportive validation
- Submitted by
- R&D Systems (provider)
- Main image
- Experimental details
- Detection of Human SNF1LK2 by Western Blot. Western blot shows lysates of human mesenchymal stem cells (MSC) grown in the absence (-) or presence (+) of StemXVivo™ Adipogenic Supplement (Catalog # CCM001). PVDF membrane was probed with 1 µg/mL of Goat Anti-Human SNF1LK2 Antigen Affinity-purified Polyclonal Antibody (Catalog # AF5737), followed by HRP-conjugated Anti-Goat IgG Secondary Antibody (Catalog # HAF109). A specific band was detected for SNF1LK2 at approximately 125 kDa (as indicated). This experiment was conducted under reducing conditions and using Immunoblot Buffer Group 1.
Supportive validation
- Submitted by
- R&D Systems (provider)
- Main image
- Experimental details
- SNF1LK2 in Human Adipocytes. SNF1LK2 was detected in immersion fixed human adipocytes using 10 µg/mL Goat Anti-Human SNF1LK2 Antigen Affinity-purified Polyclonal Antibody (Catalog # AF5737) for 3 hours at room temperature. Cells were stained with the NorthernLights™ 557-conjugated Anti-Goat IgG Secondary Antibody (red; Catalog # NL001) and counterstained with DAPI (blue). View our protocol for Fluorescent ICC Staining of Cells on Coverslips.