Rabbit Polyclonal LNP antibody. Suitable for IHC-P, WB, ICC/IF and reacts with Human samples. Cited in 2 publications. Immunogen corresponding to Recombinant Fragment Protein within Human LNPK aa 250-400.
pH: 7.2
Preservative: 0.02% Sodium azide
Constituents: 59% PBS, 40% Glycerol (glycerin, glycerine)
IHC-P | WB | ICC/IF | |
---|---|---|---|
Human | Tested | Tested | Tested |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info 1/200.00000 - 1/500.00000 | Notes Perform heat-mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol. |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info 0.04000-0.40000 µg/mL | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info 0.25000-2.00000 µg/mL | Notes - |
Endoplasmic reticulum (ER)-shaping membrane protein that plays a role in determining ER morphology (PubMed:30032983). Involved in the stabilization of nascent three-way ER tubular junctions within the ER network (PubMed:24223779, PubMed:25404289, PubMed:25548161, PubMed:27619977). May also play a role as a curvature-stabilizing protein within the three-way ER tubular junction network (PubMed:25404289). May be involved in limb development (By similarity). Is involved in central nervous system development (PubMed:30032983).
KIAA1715, LNP, LNPK, Endoplasmic reticulum junction formation protein lunapark, ER junction formation factor lunapark
Rabbit Polyclonal LNP antibody. Suitable for IHC-P, WB, ICC/IF and reacts with Human samples. Cited in 2 publications. Immunogen corresponding to Recombinant Fragment Protein within Human LNPK aa 250-400.
pH: 7.2
Preservative: 0.02% Sodium azide
Constituents: 59% PBS, 40% Glycerol (glycerin, glycerine)
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Lipid nanoparticles (LNPs) serve as important carriers in drug delivery systems especially for mRNA vaccines. They are composed of lipids and possess an average mass that varies depending on the lipid composition and payload they carry. LNPs are often used to encapsulate nucleic acids such as mRNA providing protection and enhancing cellular uptake. Expression of LNP content localizes primarily to sites where mRNA vaccines are administered delivering cargo into target cells efficiently.
Lipid nanoparticles facilitate the delivery and release of payloads like mRNA inside cells. They do not inherently form part of a biological complex but when combined with mRNA they act as a pseudo-complex that helps ensure the stability and proper cellular entry of the genetic material. LNPs utilize endocytic pathways for cellular uptake where they eventually release their payload into the cytosol through endosomal escape mechanisms.
One should note that LNPs significantly engage in endocytosis a critical cellular uptake pathway. Through their delivery mechanism they interact indirectly with proteins involved in membrane fusion and endosomal escape such as SNARE proteins and proton pumps that regulate endosomal pH levels. Moreover when carrying mRNA constructs they indirectly participate in the protein translation pathways by facilitating the mRNA's availability in the cytosol for ribosomes to function.
Lipid nanoparticles have revolutionized vaccine development prominently evidenced by their role in mRNA COVID-19 vaccines. They relate to the efficacy of vaccine-induced immune responses. Conditions such as viral infections and genetic disorders have therefore seen therapeutic advancements through the use of LNPs linked to the successful delivery of mRNA sequences coding for immunogenic proteins or therapeutic peptides. In these cases proteins like spike protein (from SARS-CoV-2) become the focus of the robust immune response facilitated through LNP-mediated delivery systems.
We have tested this species and application combination and it works. It is covered by our product promise.
We have not tested this specific species and application combination in-house, but expect it will work. It is covered by our product promise.
This species and application combination has not been tested, but we predict it will work based on strong homology. However, this combination is not covered by our product promise.
We do not recommend this combination. It is not covered by our product promise.
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All lanes: Western blot - Anti-LNP antibody (ab121416) at 0.4 µg/mL
Lane 1: U-138 MG (human glioblastoma cell line) transfected with control siRNA, whole cell lysate
Lane 2: U-138 MG transfected with target specific siRNA probe #1, whole cell lysate
Lane 3: U-138 MG transfected with target specific siRNA probe #2, whole cell lysate
Predicted band size: 48 kDa
Immunohistochemical analysis of human tonsil tissue labeling LNP with ab121416 at 1/500 dilution.
Immunofluorescent staining of Human cell line U-251MG shows positivity in nucleus but not nucleoli and cytoplasm. Recommended concentration of ab121416 1-4 µg/ml. Cells treated with PFA/Triton X-100.
Immunohistochemical analysis of human cervix tissue labeling LNP with ab121416 at 1/500 dilution.
Immunohistochemical analysis of human testis tissue labeling LNP with ab121416 at 1/500 dilution.
Western blot analysis of human U-138 MG cell lysate labeling LNP with ab121416 at 0.04 ug/ml.
All lanes: Western blot - Anti-LNP antibody (ab121416) at 0.04 µg/mL
All lanes: U-138 MG cell lysate
Performed under reducing conditions.
Predicted band size: 48 kDa
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