Antibody data
- Antibody Data
- Antigen structure
- References [1]
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- Validations
- Other assay [2]
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- Product number
- PA5-33438 - Provider product page
- Provider
- Invitrogen Antibodies
- Product name
- CMKLR1 Polyclonal Antibody
- Antibody type
- Polyclonal
- Antigen
- Synthetic peptide
- Description
- Percent identity with other species by BLAST analysis: Human, Gibbon (100%) Marmoset, Rabbit (95%) Horse (84%).
- Reactivity
- Human
- Host
- Rabbit
- Isotype
- IgG
- Vial size
- 50 µg
- 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 Pro-resolving mediators promote resolution in a human skin model of UV-killed Escherichia coli-driven acute inflammation.
Motwani MP, Colas RA, George MJ, Flint JD, Dalli J, Richard-Loendt A, De Maeyer RP, Serhan CN, Gilroy DW
JCI insight 2018 Mar 22;3(6)
JCI insight 2018 Mar 22;3(6)
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Supportive validation
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- Invitrogen Antibodies (provider)
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- Experimental details
- Figure 4 SPM receptors are differentially expressed on the endothelium and the infiltrating leukocytes -- ALX/FPR2 and ChemR23. Acute inflammation was triggered in the ventral aspect of forearm of healthy volunteers by the intradermal injection of 1.5 x 10 7 UV-killed E . coli (UVkEc) suspended in 100 mul of sterile saline. Four hours after injection, a 3-mm skin punch biopsy was taken from the inflamed site under local anesthesia. Naive skin was treated as baseline. Formalin-fixed paraffin-embedded skin sections were probed by immunohistochemistry for receptor identification. Low-magnification (x5) and high-magnification (x40) images at baseline and at the 4-hour time point are shown here for ALX/FPR2 ( A ) and ChemR23 ( B ). Red arrows highlight the endothelium and black arrow highlights the infiltrating leukocytes. Representative images from n = 3. SPM, specialized pro-resolving mediator.
- Submitted by
- Invitrogen Antibodies (provider)
- Main image
- Experimental details
- Figure 6 SPM receptor expression increases during acute inflammation. Acute inflammation was triggered in the ventral aspect of forearms of healthy volunteers by the intradermal injection of 1.5 x 10 7 UV-killed E . coli (UVkEc) suspended in 100 mul of sterile saline. Four hours after injection, a 3-mm skin punch biopsy was taken from the inflamed site under local anaesthesia. Formalin-fixed paraffin-embedded skin sections were probed by immunohistochemistry for receptor identification, as shown in Figures 4 and 5 . Increase in receptor expression from baseline to 4 hours following UVkEc injection for ALX/FPR2 ( A ), ChemR23 ( B ), GPR18 ( C ), and GPR32 ( D ) is shown here. Data expressed as box-and-whisker plots (box representing the median and the whiskers representing the maximum-minimum values). Statistical comparison between baseline and 4-hour expression was assessed by Wilcoxon's matched-pairs test. n = 3 for each time point. * P < 0.05. SPM, specialized pro-resolving mediator.