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fluorescence microscope equipped with a 63× oil-immersion objective (na 1.4) carl zeiss axioplan 2  (Carl Zeiss)
90
Carl Zeiss fluorescence microscope equipped with a 63× oil-immersion objective (na 1.4) carl zeiss axioplan 2
Fluorescence Microscope Equipped With A 63× Oil Immersion Objective (Na 1.4) Carl Zeiss Axioplan 2, supplied by Carl Zeiss, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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fluorescence microscope equipped with a 63× oil-immersion objective (na 1.4) carl zeiss axioplan 2 - by Bioz Stars, 2026-03
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63x/1.4 na oil immersion objective  (Carl Zeiss)
90
Carl Zeiss 63x/1.4 na oil immersion objective
Screening and identification of nanobodies against pXCR1 protein. ( A ) Schematic diagram of antigen-specific nanobody screening. ( B ) SDS-PAGE analysis of the purification of pXCR1 protein. ( C ) Western blotting identification of His-pXCR1 protein using mouse anti-His antibody as the primary antibody. ( D ) After 5 immunization, the serum antibody titers against pXCR1 protein. ( E ) Enrichment of the specific VHH phage particles against pXCR1 protein after 4 rounds of bio-panning. ( F and G ) ELISA analysis of periplasmic extracts reacted with pXCR1 protein from 72 clones. ( H ) Amino acid sequence alignment of isolated Nbs. CDR3 variable domain was used to distinguish different Nbs. ( I ) ELISA was performed to detect the affinity of Nb6, Nb21 and Nb50 to pXCR1 protein. ( J ) ELISA analysis of the reaction specificity of Nb6, Nb21 and Nb50 with pXCR1. ( K ) Co-ip identification of Nb21 interacted with pXCR1 protein, Nb35 was used as a negative control. ( L ) Confocal analysis of screened Nb21 reactivity with pXCR1 protein. Images were obtained using a Zeiss <t>LSM510</t> laser scanning inverted confocal microscope with a Zeiss 63X/1.4 NA oil immersion objective. Scale bar: 10 μm
63x/1.4 Na Oil Immersion Objective, supplied by Carl Zeiss, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/63x/1.4 na oil immersion objective/product/Carl Zeiss
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63x/1.4 na oil immersion objective - by Bioz Stars, 2026-03
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oil immersion objective at 1200× magnification zeiss axioskope microscope  (Carl Zeiss)
90
Carl Zeiss oil immersion objective at 1200× magnification zeiss axioskope microscope
Screening and identification of nanobodies against pXCR1 protein. ( A ) Schematic diagram of antigen-specific nanobody screening. ( B ) SDS-PAGE analysis of the purification of pXCR1 protein. ( C ) Western blotting identification of His-pXCR1 protein using mouse anti-His antibody as the primary antibody. ( D ) After 5 immunization, the serum antibody titers against pXCR1 protein. ( E ) Enrichment of the specific VHH phage particles against pXCR1 protein after 4 rounds of bio-panning. ( F and G ) ELISA analysis of periplasmic extracts reacted with pXCR1 protein from 72 clones. ( H ) Amino acid sequence alignment of isolated Nbs. CDR3 variable domain was used to distinguish different Nbs. ( I ) ELISA was performed to detect the affinity of Nb6, Nb21 and Nb50 to pXCR1 protein. ( J ) ELISA analysis of the reaction specificity of Nb6, Nb21 and Nb50 with pXCR1. ( K ) Co-ip identification of Nb21 interacted with pXCR1 protein, Nb35 was used as a negative control. ( L ) Confocal analysis of screened Nb21 reactivity with pXCR1 protein. Images were obtained using a Zeiss <t>LSM510</t> laser scanning inverted confocal microscope with a Zeiss 63X/1.4 NA oil immersion objective. Scale bar: 10 μm
Oil Immersion Objective At 1200× Magnification Zeiss Axioskope Microscope, supplied by Carl Zeiss, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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oil immersion objective at 1200× magnification zeiss axioskope microscope - by Bioz Stars, 2026-03
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immersion oil type ldf  (Cargille Laboratories)
90
Cargille Laboratories immersion oil type ldf
Screening and identification of nanobodies against pXCR1 protein. ( A ) Schematic diagram of antigen-specific nanobody screening. ( B ) SDS-PAGE analysis of the purification of pXCR1 protein. ( C ) Western blotting identification of His-pXCR1 protein using mouse anti-His antibody as the primary antibody. ( D ) After 5 immunization, the serum antibody titers against pXCR1 protein. ( E ) Enrichment of the specific VHH phage particles against pXCR1 protein after 4 rounds of bio-panning. ( F and G ) ELISA analysis of periplasmic extracts reacted with pXCR1 protein from 72 clones. ( H ) Amino acid sequence alignment of isolated Nbs. CDR3 variable domain was used to distinguish different Nbs. ( I ) ELISA was performed to detect the affinity of Nb6, Nb21 and Nb50 to pXCR1 protein. ( J ) ELISA analysis of the reaction specificity of Nb6, Nb21 and Nb50 with pXCR1. ( K ) Co-ip identification of Nb21 interacted with pXCR1 protein, Nb35 was used as a negative control. ( L ) Confocal analysis of screened Nb21 reactivity with pXCR1 protein. Images were obtained using a Zeiss <t>LSM510</t> laser scanning inverted confocal microscope with a Zeiss 63X/1.4 NA oil immersion objective. Scale bar: 10 μm
Immersion Oil Type Ldf, supplied by Cargille Laboratories, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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oil immersion 40×/1.3 numerical aperture (na) objective  (Carl Zeiss)
90
Carl Zeiss oil immersion 40×/1.3 numerical aperture (na) objective
Screening and identification of nanobodies against pXCR1 protein. ( A ) Schematic diagram of antigen-specific nanobody screening. ( B ) SDS-PAGE analysis of the purification of pXCR1 protein. ( C ) Western blotting identification of His-pXCR1 protein using mouse anti-His antibody as the primary antibody. ( D ) After 5 immunization, the serum antibody titers against pXCR1 protein. ( E ) Enrichment of the specific VHH phage particles against pXCR1 protein after 4 rounds of bio-panning. ( F and G ) ELISA analysis of periplasmic extracts reacted with pXCR1 protein from 72 clones. ( H ) Amino acid sequence alignment of isolated Nbs. CDR3 variable domain was used to distinguish different Nbs. ( I ) ELISA was performed to detect the affinity of Nb6, Nb21 and Nb50 to pXCR1 protein. ( J ) ELISA analysis of the reaction specificity of Nb6, Nb21 and Nb50 with pXCR1. ( K ) Co-ip identification of Nb21 interacted with pXCR1 protein, Nb35 was used as a negative control. ( L ) Confocal analysis of screened Nb21 reactivity with pXCR1 protein. Images were obtained using a Zeiss <t>LSM510</t> laser scanning inverted confocal microscope with a Zeiss 63X/1.4 NA oil immersion objective. Scale bar: 10 μm
Oil Immersion 40×/1.3 Numerical Aperture (Na) Objective, supplied by Carl Zeiss, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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oil immersion 40×/1.3 numerical aperture (na) objective - by Bioz Stars, 2026-03
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100× oil immersion objective uplan cfi plan apochromat lambda d 100× oil  (Nikon)
90
Nikon 100× oil immersion objective uplan cfi plan apochromat lambda d 100× oil
Screening and identification of nanobodies against pXCR1 protein. ( A ) Schematic diagram of antigen-specific nanobody screening. ( B ) SDS-PAGE analysis of the purification of pXCR1 protein. ( C ) Western blotting identification of His-pXCR1 protein using mouse anti-His antibody as the primary antibody. ( D ) After 5 immunization, the serum antibody titers against pXCR1 protein. ( E ) Enrichment of the specific VHH phage particles against pXCR1 protein after 4 rounds of bio-panning. ( F and G ) ELISA analysis of periplasmic extracts reacted with pXCR1 protein from 72 clones. ( H ) Amino acid sequence alignment of isolated Nbs. CDR3 variable domain was used to distinguish different Nbs. ( I ) ELISA was performed to detect the affinity of Nb6, Nb21 and Nb50 to pXCR1 protein. ( J ) ELISA analysis of the reaction specificity of Nb6, Nb21 and Nb50 with pXCR1. ( K ) Co-ip identification of Nb21 interacted with pXCR1 protein, Nb35 was used as a negative control. ( L ) Confocal analysis of screened Nb21 reactivity with pXCR1 protein. Images were obtained using a Zeiss <t>LSM510</t> laser scanning inverted confocal microscope with a Zeiss 63X/1.4 NA oil immersion objective. Scale bar: 10 μm
100× Oil Immersion Objective Uplan Cfi Plan Apochromat Lambda D 100× Oil, supplied by Nikon, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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100× oil immersion objective uplan cfi plan apochromat lambda d 100× oil - by Bioz Stars, 2026-03
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c–apochromat 63 ×/1.4 oil immersion objective  (Carl Zeiss)
90
Carl Zeiss c–apochromat 63 ×/1.4 oil immersion objective
Screening and identification of nanobodies against pXCR1 protein. ( A ) Schematic diagram of antigen-specific nanobody screening. ( B ) SDS-PAGE analysis of the purification of pXCR1 protein. ( C ) Western blotting identification of His-pXCR1 protein using mouse anti-His antibody as the primary antibody. ( D ) After 5 immunization, the serum antibody titers against pXCR1 protein. ( E ) Enrichment of the specific VHH phage particles against pXCR1 protein after 4 rounds of bio-panning. ( F and G ) ELISA analysis of periplasmic extracts reacted with pXCR1 protein from 72 clones. ( H ) Amino acid sequence alignment of isolated Nbs. CDR3 variable domain was used to distinguish different Nbs. ( I ) ELISA was performed to detect the affinity of Nb6, Nb21 and Nb50 to pXCR1 protein. ( J ) ELISA analysis of the reaction specificity of Nb6, Nb21 and Nb50 with pXCR1. ( K ) Co-ip identification of Nb21 interacted with pXCR1 protein, Nb35 was used as a negative control. ( L ) Confocal analysis of screened Nb21 reactivity with pXCR1 protein. Images were obtained using a Zeiss <t>LSM510</t> laser scanning inverted confocal microscope with a Zeiss 63X/1.4 NA oil immersion objective. Scale bar: 10 μm
C–Apochromat 63 ×/1.4 Oil Immersion Objective, supplied by Carl Zeiss, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/c–apochromat 63 ×/1.4 oil immersion objective/product/Carl Zeiss
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plan apo 60xa/1.40 oil immersion lens  (Nikon)
90
Nikon plan apo 60xa/1.40 oil immersion lens
Screening and identification of nanobodies against pXCR1 protein. ( A ) Schematic diagram of antigen-specific nanobody screening. ( B ) SDS-PAGE analysis of the purification of pXCR1 protein. ( C ) Western blotting identification of His-pXCR1 protein using mouse anti-His antibody as the primary antibody. ( D ) After 5 immunization, the serum antibody titers against pXCR1 protein. ( E ) Enrichment of the specific VHH phage particles against pXCR1 protein after 4 rounds of bio-panning. ( F and G ) ELISA analysis of periplasmic extracts reacted with pXCR1 protein from 72 clones. ( H ) Amino acid sequence alignment of isolated Nbs. CDR3 variable domain was used to distinguish different Nbs. ( I ) ELISA was performed to detect the affinity of Nb6, Nb21 and Nb50 to pXCR1 protein. ( J ) ELISA analysis of the reaction specificity of Nb6, Nb21 and Nb50 with pXCR1. ( K ) Co-ip identification of Nb21 interacted with pXCR1 protein, Nb35 was used as a negative control. ( L ) Confocal analysis of screened Nb21 reactivity with pXCR1 protein. Images were obtained using a Zeiss <t>LSM510</t> laser scanning inverted confocal microscope with a Zeiss 63X/1.4 NA oil immersion objective. Scale bar: 10 μm
Plan Apo 60xa/1.40 Oil Immersion Lens, supplied by Nikon, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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plan neofluor oil-immersion objectives  (Carl Zeiss)
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Carl Zeiss plan neofluor oil-immersion objectives
Screening and identification of nanobodies against pXCR1 protein. ( A ) Schematic diagram of antigen-specific nanobody screening. ( B ) SDS-PAGE analysis of the purification of pXCR1 protein. ( C ) Western blotting identification of His-pXCR1 protein using mouse anti-His antibody as the primary antibody. ( D ) After 5 immunization, the serum antibody titers against pXCR1 protein. ( E ) Enrichment of the specific VHH phage particles against pXCR1 protein after 4 rounds of bio-panning. ( F and G ) ELISA analysis of periplasmic extracts reacted with pXCR1 protein from 72 clones. ( H ) Amino acid sequence alignment of isolated Nbs. CDR3 variable domain was used to distinguish different Nbs. ( I ) ELISA was performed to detect the affinity of Nb6, Nb21 and Nb50 to pXCR1 protein. ( J ) ELISA analysis of the reaction specificity of Nb6, Nb21 and Nb50 with pXCR1. ( K ) Co-ip identification of Nb21 interacted with pXCR1 protein, Nb35 was used as a negative control. ( L ) Confocal analysis of screened Nb21 reactivity with pXCR1 protein. Images were obtained using a Zeiss <t>LSM510</t> laser scanning inverted confocal microscope with a Zeiss 63X/1.4 NA oil immersion objective. Scale bar: 10 μm
Plan Neofluor Oil Immersion Objectives, supplied by Carl Zeiss, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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oil-immersion objective lens cfi apo tirf 60x oil  (Nikon)
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Nikon oil-immersion objective lens cfi apo tirf 60x oil
Screening and identification of nanobodies against pXCR1 protein. ( A ) Schematic diagram of antigen-specific nanobody screening. ( B ) SDS-PAGE analysis of the purification of pXCR1 protein. ( C ) Western blotting identification of His-pXCR1 protein using mouse anti-His antibody as the primary antibody. ( D ) After 5 immunization, the serum antibody titers against pXCR1 protein. ( E ) Enrichment of the specific VHH phage particles against pXCR1 protein after 4 rounds of bio-panning. ( F and G ) ELISA analysis of periplasmic extracts reacted with pXCR1 protein from 72 clones. ( H ) Amino acid sequence alignment of isolated Nbs. CDR3 variable domain was used to distinguish different Nbs. ( I ) ELISA was performed to detect the affinity of Nb6, Nb21 and Nb50 to pXCR1 protein. ( J ) ELISA analysis of the reaction specificity of Nb6, Nb21 and Nb50 with pXCR1. ( K ) Co-ip identification of Nb21 interacted with pXCR1 protein, Nb35 was used as a negative control. ( L ) Confocal analysis of screened Nb21 reactivity with pXCR1 protein. Images were obtained using a Zeiss <t>LSM510</t> laser scanning inverted confocal microscope with a Zeiss 63X/1.4 NA oil immersion objective. Scale bar: 10 μm
Oil Immersion Objective Lens Cfi Apo Tirf 60x Oil, supplied by Nikon, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


Screening and identification of nanobodies against pXCR1 protein. ( A ) Schematic diagram of antigen-specific nanobody screening. ( B ) SDS-PAGE analysis of the purification of pXCR1 protein. ( C ) Western blotting identification of His-pXCR1 protein using mouse anti-His antibody as the primary antibody. ( D ) After 5 immunization, the serum antibody titers against pXCR1 protein. ( E ) Enrichment of the specific VHH phage particles against pXCR1 protein after 4 rounds of bio-panning. ( F and G ) ELISA analysis of periplasmic extracts reacted with pXCR1 protein from 72 clones. ( H ) Amino acid sequence alignment of isolated Nbs. CDR3 variable domain was used to distinguish different Nbs. ( I ) ELISA was performed to detect the affinity of Nb6, Nb21 and Nb50 to pXCR1 protein. ( J ) ELISA analysis of the reaction specificity of Nb6, Nb21 and Nb50 with pXCR1. ( K ) Co-ip identification of Nb21 interacted with pXCR1 protein, Nb35 was used as a negative control. ( L ) Confocal analysis of screened Nb21 reactivity with pXCR1 protein. Images were obtained using a Zeiss LSM510 laser scanning inverted confocal microscope with a Zeiss 63X/1.4 NA oil immersion objective. Scale bar: 10 μm

Journal: Journal of Nanobiotechnology

Article Title: Biomimetic phosphorus dendrimer multi-epitope nanovaccine enhances humoral and cellular immune response against African swine fever virus

doi: 10.1186/s12951-025-03593-7

Figure Lengend Snippet: Screening and identification of nanobodies against pXCR1 protein. ( A ) Schematic diagram of antigen-specific nanobody screening. ( B ) SDS-PAGE analysis of the purification of pXCR1 protein. ( C ) Western blotting identification of His-pXCR1 protein using mouse anti-His antibody as the primary antibody. ( D ) After 5 immunization, the serum antibody titers against pXCR1 protein. ( E ) Enrichment of the specific VHH phage particles against pXCR1 protein after 4 rounds of bio-panning. ( F and G ) ELISA analysis of periplasmic extracts reacted with pXCR1 protein from 72 clones. ( H ) Amino acid sequence alignment of isolated Nbs. CDR3 variable domain was used to distinguish different Nbs. ( I ) ELISA was performed to detect the affinity of Nb6, Nb21 and Nb50 to pXCR1 protein. ( J ) ELISA analysis of the reaction specificity of Nb6, Nb21 and Nb50 with pXCR1. ( K ) Co-ip identification of Nb21 interacted with pXCR1 protein, Nb35 was used as a negative control. ( L ) Confocal analysis of screened Nb21 reactivity with pXCR1 protein. Images were obtained using a Zeiss LSM510 laser scanning inverted confocal microscope with a Zeiss 63X/1.4 NA oil immersion objective. Scale bar: 10 μm

Article Snippet: Images were obtained using a Zeiss LSM510 laser scanning inverted confocal microscope with a Zeiss 63X/1.4 NA oil immersion objective.

Techniques: SDS Page, Purification, Western Blot, Enzyme-linked Immunosorbent Assay, Clone Assay, Sequencing, Isolation, Co-Immunoprecipitation Assay, Negative Control, Microscopy