Antibody data
- Antibody Data
- Antigen structure
- References [1]
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- Validations
- Other assay [1]
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- Product number
- PA5-31401 - Provider product page
- Provider
- Invitrogen Antibodies
- Product name
- SPRY4 Polyclonal Antibody
- Antibody type
- Polyclonal
- Antigen
- Recombinant protein fragment
- Description
- Recommended positive controls: NT2D1, mouse brain. Predicted reactivity: Mouse (94%), Rat (94%), Sheep (94%), Bovine (95%). Store product as a concentrated solution. Centrifuge briefly prior to opening the vial.
- Reactivity
- Human, Mouse
- Host
- Rabbit
- Isotype
- IgG
- Vial size
- 100 µL
- Concentration
- 1 mg/mL
- Storage
- Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Submitted references The Role of the miR-21/SPRY2 Axis in Modulating Proangiogenic Factors, Epithelial Phenotypes, and Wound Healing in Corneal Epithelial Cells.
Zhang Y, Yuan F, Liu L, Chen Z, Ma X, Lin Z, Zou J
Investigative ophthalmology & visual science 2019 Sep 3;60(12):3854-3862
Investigative ophthalmology & visual science 2019 Sep 3;60(12):3854-3862
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Supportive validation
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- Invitrogen Antibodies (provider)
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- Experimental details
- Figure 2 SPRY2 is a direct target of miR-21 in corneal epithelial cells. Corneal epithelial cells were treated with miR-21 inhibitor and exposed to TGF-beta1 (T), 1% O 2 (H), or TGF-beta1 plus 1% O 2 (T+H). The protein levels of SPRY1, SPRY2, SPRY4, and p-ERK, were determined by Western blotting (A) followed by densitometry analysis using ImageJ software (B). Tubulin was used as the loading control. (C) miR-21 and its putative binding sequences in the mouse 3'-UTR of Spry2. The binding sequences in the complementary sites were replaced by the indicated nucleotides to produce mutant Spry2 3'-UTR luciferase reporter constructs. Marked sequences represent the conserved complementary nucleotides of the miR-21 binding sequence in humans and various mammals. (D, E) Luciferase activity of the wild-type and mutated 3'-UTR of Spry2 treated with miR-21 mimic (D) or inhibitor (E). *P < 0.05, **P < 0.01, ***P < 0.001, versus the untreated group (B) or mimic NC (D) or inhibitor NC group (E). Experiments were performed in triplicate.