Background: Phytophthora capsici root rot (PRR) is a disastrous disease in peppers (Capsicum spp.) caused by soilborne oomycete with typical symptoms of necrosis and constriction at the basal stem and consequent plant wilting.
Most studies on the QTL mapping of P. capsici resistance suggested a consensus broad-spectrum QTL on chromosome 5 named Pc.5.1 regardless of P. capsici isolates and resistant resources. In addition, all these reports proposed NBS-ARC domain genes as candidate genes controlling resistance.
Results: We screened out 10 PRR-resistant resources from 160 Capsicum germplasm and inspected the response of locus Pc.5.1 and NBS-ARC genes during P. capsici infection by comparing the root transcriptomes of resistant pepper 305R and susceptible pepper 372S.
To dissect the structure of Pc.5.1, we anchored genetic markers onto pepper genomic sequence and made an extended Pc5.1 (Ext-Pc5.1) located at 8.35 Mb-38.13 Mb on chromosome 5 which covered all Pc5.1 reported in publications.
A total of 571 NBS-ARC genes were mined from the genome of pepper CM334 and 34 genes were significantly affected by P. capsici infection in either 305R or 372S. Only 5 inducible NBS-ARC genes had LRR domains and none of them was positioned at Ext-Pc5.1. Ext-Pc5.1 did show strong response to P. capsici infection and there were a total of 44 differentially expressed genes (DEGs), but no candidate genes proposed by previous publications was included. Snakin-1 (SN1), a well-known antimicrobial peptide gene located at Pc5.1, was significantly decreased in 372S but not in 305R.
Moreover, there was an impressive upregulation of sugar pathway genes in 305R, which was confirmed by metabolite analysis of roots. The biological processes of histone methylation, histone phosphorylation, DNA methylation, and nucleosome assembly were strongly activated in 305R but not in 372S, indicating an epigenetic-related defense mechanism.
Conclusions: Those NBS-ARC genes that were suggested to contribute to Pc5.1 in previous publications did not show any significant response in P. capsici infection and there were no significant differences of these genes in transcription levels between 305R and 372S.
Other pathogen defense-related genes like SN1 might account for Pc5.1. Our study also proposed the important role of sugar and epigenetic regulation in the defense against P. capsici.
Bioinformatics analysis and identification of genes and molecular pathways in steroid-induced osteonecrosis of the femoral head
Background: Steroid-induced osteonecrosis of the femoral head (ONFH) is a common hip joint disease and is difficult to be diagnosed early. At present, the pathogenesis of steroid-induced ONFH remains unclear, and recognized and effective diagnostic biomarkers are deficient. The present study aimed to identify potentially important genes and signaling pathways involved in steroid-induced ONFH and investigate their molecular mechanisms.
Methods: Microarray data sets GSE123568 (peripheral blood) and GSE74089 (cartilage) were obtained from the Gene Expression Omnibus database, including 34 ONFH samples and 14 control samples. Morpheus software and Venn diagram were used to identify DEGs and co-expressed DEGs, respectively. Besides, we conducted Kyoto Encyclopedia of Genome (KEGG) and gene ontology (GO) pathway enrichment analysis.
We construct a protein-protein interaction (PPI) network through GEO2R and used cytoHubba to divide the PPI network into multiple sub-networks. Additionally, quantitative real-time polymerase chain reaction (qRT-PCR) was performed to verify the bioinformatics analysis results.
Results: A total of 118 intersecting DEGs were obtained between the peripheral blood and cartilage samples, including 40 upregulated genes and 78 downregulated genes. Then, GO and KEGG pathway enrichment analysis revealed that upregulated DEGs focused on the signaling pathways related to staphylococcus aureus infection, leishmaniasis, antigen processing, and presentation, as well as asthma and graft-versus-host disease.
Downregulated genes were concentrated in the FoxO signaling pathway, AMPK signaling pathway, signaling pathway regulating stem cell pluripotency, and mTOR signaling pathway. Some hub genes with high interactions such as CXCR1, FPR1, MAPK1, FOXO3, FPR2, CXCR2, and TYROBP were identified in the PPI network.
The results of qRT-PCR demonstrated that CXCR1, FPR1, and TYROBP were upregulated while MAPK1 was downregulated in peripheral blood of steroid-induced ONFH patients. This was consistent with the bioinformatics analysis.
Conclusions: The present study would provide novel insight into the genes and associated pathways involved in steroid-induced ONFH. CXCR1, FPR1, TYROBP, and MAPK1 may be used as potential drug targets and biomarkers for the diagnosis and prognosis of steroid-induced ONFH.
stjosephs-hospital
Cultural Evolution of Genetic Heritability
Behavioral genetics and cultural evolution have both revolutionized our understanding of human behavior-largely independent of each other. Here we reconcile these two fields under a dual inheritance framework, offering a more nuanced understanding of the interaction between genes and culture.
Going beyond typical analyses of gene-environment interactions, we describe the cultural dynamics that shape these interactions by shaping the environment and population structure. A cultural evolutionary approach can explain, for example, how factors such as rates of innovation and diffusion, density of cultural sub-groups, and tolerance for behavioral diversity impact heritability estimates, thus yielding predictions for different social contexts.
- Moreover, when cumulative culture functionally overlaps with genes, genetic effects become masked, unmasked, or even reversed, and the causal effects of an identified gene become confounded with features of the cultural environment.
- The manner of confounding is specific to a particular society at a particular time, but a WEIRD (Western, educated, industrialized, rich, democratic) sampling problem obscures this boundedness.
- Cultural evolutionary dynamics are typically missing from models of gene-to-phenotype causality, hindering generalizability of genetic effects across societies and across time.
- We lay out a reconciled framework and use it to predict the ways in which heritability should differ between societies, between socioeconomic levels and other groupings within some societies but not others, and over the life course.
- An integrated cultural evolutionary behavioral genetic approach cuts through the nature-nurture debate and helps resolve controversies in topics such as IQ.
 Polyclonal Goat anti-GST α-form |
|
GST-ANTI-1 |
Detroit R&D |
50 uL |
EUR 280 |
 Polyclonal Goat anti-GST μ-form |
|
GST-ANTI-2 |
Detroit R&D |
50 uL |
EUR 280 |
 Polyclonal Goat anti-GST p-form |
|
GST-ANTI-3 |
Detroit R&D |
50 uL |
EUR 280 |
) Human Transcription factor p65 protein (NFKB3) |
|
1-CSB-RP039844h |
Cusabio |
-
EUR 380.00
-
EUR 214.00
-
EUR 1309.00
-
EUR 560.00
-
EUR 873.00
-
EUR 262.00
|
-
100ug
-
10ug
-
1MG
-
200ug
-
500ug
-
50ug
|
|
|
|
Description: Recombinant Human Transcription factor p65 protein(NFKB3),partial expressed in E.coli |
Human Transcription factor p65 protein (NFKB3) |
|
1-CSB-RP039874h |
Cusabio |
-
EUR 380.00
-
EUR 214.00
-
EUR 1309.00
-
EUR 560.00
-
EUR 873.00
-
EUR 262.00
|
-
100ug
-
10ug
-
1MG
-
200ug
-
500ug
-
50ug
|
|
|
|
Description: Recombinant Human Transcription factor p65 protein(NFKB3),partial expressed in E.coli |
 ELISA Kit) Human Transcription factor p65 / NFKB3 (RELA) ELISA Kit |
|
20-abx152945 |
Abbexa |
-
EUR 6642.00
-
EUR 3542.00
-
EUR 825.00
|
-
10 × 96 tests
-
5 × 96 tests
-
96 tests
|
|
|
Human Transcription factor p65 / NFKB3 (RELA) ELISA Kit |
|
abx570125-96tests |
Abbexa |
96 tests |
EUR 668 |
|
|
 ELISA Kit) Mouse Transcription factor p65 / NFKB3 (RELA) ELISA Kit |
|
abx570127-96tests |
Abbexa |
96 tests |
EUR 668 |
|
|
 ELISA Kit) Rat Transcription factor p65 / NFKB3 (RELA) ELISA Kit |
|
abx255851-96tests |
Abbexa |
96 tests |
EUR 668 |
|
|
Human Transcription factor p65 / NFKB3 (RELA) ELISA Kit |
|
abx252815-96tests |
Abbexa |
96 tests |
EUR 668 |
|
|
Mouse Transcription factor p65 / NFKB3 (RELA) ELISA Kit |
|
abx254289-96tests |
Abbexa |
96 tests |
EUR 668 |
|
|
 ELISA Kit) Pig Transcription factor p65 / NFKB3 (RELA) ELISA Kit |
|
abx361108-96tests |
Abbexa |
96 tests |
EUR 825 |
|
|
 ELISA Kit) Rabbit Transcription factor p65 / NFKB3 (RELA) ELISA Kit |
|
abx362582-96tests |
Abbexa |
96 tests |
EUR 825 |
|
|
 ELISA Kit) Sheep Transcription factor p65 / NFKB3 (RELA) ELISA Kit |
|
abx364265-96tests |
Abbexa |
96 tests |
EUR 926 |
|
|
 ELISA Kit) Monkey Transcription factor p65 / NFKB3 (RELA) ELISA Kit |
|
abx359107-96tests |
Abbexa |
96 tests |
EUR 825 |
|
|
 ELISA Kit) Chicken Transcription factor p65 / NFKB3 (RELA) ELISA Kit |
|
abx357192-96tests |
Abbexa |
96 tests |
EUR 825 |
|
|
Rat Transcription factor p65 / NFKB3 (RELA) ELISA Kit |
|
20-abx156040 |
Abbexa |
-
EUR 7237.00
-
EUR 3855.00
-
EUR 895.00
|
-
10 × 96 tests
-
5 × 96 tests
-
96 tests
|
|
|
 ELISA Kit) Guinea pig Transcription factor p65 / NFKB3 (RELA) ELISA Kit |
|
abx357262-96tests |
Abbexa |
96 tests |
EUR 825 |
|
|
 Anti-Anti-SEPT6 antibody antibody |
|
STJ11100949 |
St John's Laboratory |
100 µl |
EUR 277 |
|
Description: This gene is a member of the septin family of GTPases. Members of this family are required for cytokinesis. One version of pediatric acute myeloid leukemia is the result of a reciprocal translocation between chromosomes 11 and X, with the breakpoint associated with the genes encoding the mixed-lineage leukemia and septin 2 proteins. This gene encodes four transcript variants encoding three distinct isoforms. An additional transcript variant has been identified, but its biological validity has not been determined. |
 Anti-Anti-SEPT9 Antibody antibody |
|
STJ111369 |
St John's Laboratory |
100 µl |
EUR 277 |
|
Description: This gene is a member of the septin family involved in cytokinesis and cell cycle control. This gene is a candidate for the ovarian tumor suppressor gene. Mutations in this gene cause hereditary neuralgic amyotrophy, also known as neuritis with brachial predilection. A chromosomal translocation involving this gene on chromosome 17 and the MLL gene on chromosome 11 results in acute myelomonocytic leukemia. Multiple alternatively spliced transcript variants encoding different isoforms have been described. |
 Anti-Anti-SEPT4 Antibody antibody |
|
STJ112276 |
St John's Laboratory |
100 µl |
EUR 277 |
|
Description: This gene is a member of the septin family of nucleotide binding proteins, originally described in yeast as cell division cycle regulatory proteins. Septins are highly conserved in yeast, Drosophila, and mouse, and appear to regulate cytoskeletal organization. Disruption of septin function disturbs cytokinesis and results in large multinucleate or polyploid cells. This gene is highly expressed in brain and heart. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. One of the isoforms (known as ARTS) is distinct; it is localized to the mitochondria, and has a role in apoptosis and cancer. |
 Anti-Anti-SEPT5 Antibody antibody |
|
STJ25477 |
St John's Laboratory |
100 µl |
EUR 277 |
|
Description: This gene is a member of the septin gene family of nucleotide binding proteins, originally described in yeast as cell division cycle regulatory proteins. Septins are highly conserved in yeast, Drosophila, and mouse and appear to regulate cytoskeletal organization. Disruption of septin function disturbs cytokinesis and results in large multinucleate or polyploid cells. This gene is mapped to 22q11, the region frequently deleted in DiGeorge and velocardiofacial syndromes. A translocation involving the MLL gene and this gene has also been reported in patients with acute myeloid leukemia. Alternative splicing results in multiple transcript variants. The presence of a non-consensus polyA signal (AACAAT) in this gene also results in read-through transcription into the downstream neighboring gene (GP1BB; platelet glycoprotein Ib), whereby larger, non-coding transcripts are produced. |
 Anti-Anti-SEPT8 Antibody antibody |
|
STJ25479 |
St John's Laboratory |
100 µl |
EUR 277 |
|
Description: This gene is a member of the septin family of nucleotide binding proteins, originally described in yeast as cell division cycle regulatory proteins. Septins are highly conserved in yeast, Drosophila, and mouse, and appear to regulate cytoskeletal organization. Disruption of septin function disturbs cytokinesis and results in large multinucleate or polyploid cells. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. |
 Anti-Anti-SEPT7 Antibody antibody |
|
STJ28963 |
St John's Laboratory |
100 µl |
EUR 277 |
|
Description: This gene encodes a protein that is highly similar to the CDC10 protein of Saccharomyces cerevisiae. The protein also shares similarity with Diff 6 of Drosophila and with H5 of mouse. Each of these similar proteins, including the yeast CDC10, contains a GTP-binding motif. The yeast CDC10 protein is a structural component of the 10 nm filament which lies inside the cytoplasmic membrane and is essential for cytokinesis. This human protein functions in gliomagenesis and in the suppression of glioma cell growth, and it is required for the association of centromere-associated protein E with the kinetochore. Alternative splicing results in multiple transcript variants. Several related pseudogenes have been identified on chromosomes 5, 7, 9, 10, 11, 14, 17 and 19. |
Anti-Anti-SEPT7 Antibody antibody |
|
STJ116214 |
St John's Laboratory |
100 µl |
EUR 277 |
|
Description: This gene encodes a protein that is highly similar to the CDC10 protein of Saccharomyces cerevisiae. The protein also shares similarity with Diff 6 of Drosophila and with H5 of mouse. Each of these similar proteins, including the yeast CDC10, contains a GTP-binding motif. The yeast CDC10 protein is a structural component of the 10 nm filament which lies inside the cytoplasmic membrane and is essential for cytokinesis. This human protein functions in gliomagenesis and in the suppression of glioma cell growth, and it is required for the association of centromere-associated protein E with the kinetochore. Alternative splicing results in multiple transcript variants. Several related pseudogenes have been identified on chromosomes 5, 7, 9, 10, 11, 14, 17 and 19. |
Anti-Anti-SEPT8 Antibody antibody |
|
STJ117206 |
St John's Laboratory |
100 µl |
EUR 277 |
|
Description: This gene is a member of the septin family of nucleotide binding proteins, originally described in yeast as cell division cycle regulatory proteins. Septins are highly conserved in yeast, Drosophila, and mouse, and appear to regulate cytoskeletal organization. Disruption of septin function disturbs cytokinesis and results in large multinucleate or polyploid cells. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. |
 Anti-Anti-SEPT12 Antibody antibody |
|
STJ117759 |
St John's Laboratory |
100 µl |
EUR 277 |
|
Description: This gene encodes a guanine-nucleotide binding protein and member of the septin family of cytoskeletal GTPases. Septins play important roles in cytokinesis, exocytosis, embryonic development, and membrane dynamics. Multiple transcript variants encoding different isoforms have been found for this gene. |
 Anti-Anti-SEPT1 antibody antibody |
|
STJ119580 |
St John's Laboratory |
100 µl |
EUR 277 |
|
Description: This gene is a member of the septin family of GTPases. Members of this family are required for cytokinesis and the maintenance of cellular morphology. This gene encodes a protein that can form homo- and heterooligomeric filaments, and may contribute to the formation of neurofibrillary tangles in Alzheimer's disease. Alternatively spliced transcript variants have been found but the full-length nature of these variants has not been determined. [provided by RefSeq, Dec 2012] |
Anti-Anti-SEPT5 Antibody antibody |
|
STJ114819 |
St John's Laboratory |
100 µl |
EUR 277 |
|
Description: This gene is a member of the septin gene family of nucleotide binding proteins, originally described in yeast as cell division cycle regulatory proteins. Septins are highly conserved in yeast, Drosophila, and mouse and appear to regulate cytoskeletal organization. Disruption of septin function disturbs cytokinesis and results in large multinucleate or polyploid cells. This gene is mapped to 22q11, the region frequently deleted in DiGeorge and velocardiofacial syndromes. A translocation involving the MLL gene and this gene has also been reported in patients with acute myeloid leukemia. Alternative splicing results in multiple transcript variants. The presence of a non-consensus polyA signal (AACAAT) in this gene also results in read-through transcription into the downstream neighboring gene (GP1BB; platelet glycoprotein Ib), whereby larger, non-coding transcripts are produced. |
 Anti-Anti-DDB1 Antibody |
|
A00333 |
BosterBio |
100uL |
EUR 455 |
|
Description: Rabbit Polyclonal DDB1 Antibody. Validated in IP and tested in Human, Mouse. |
 ELISA Kit) Human Anti-Anti-Sperm Antibody Antibody (Anti-AsAb) ELISA Kit |
|
AEA465Hu-10x96wellstestplate |
Cloud-Clone |
10x96-wells test plate |
EUR 5647.8 |
|
|
|
Description: This is Competitive Enzyme-linked immunosorbent assay for Antibody Detection.detection of Human Anti-Anti-Sperm Antibody Antibody (Anti-AsAb) in serum, plasma and other biological fluids. |
Human Anti-Anti-Sperm Antibody Antibody (Anti-AsAb) ELISA Kit |
|
AEA465Hu-1x48wellstestplate |
Cloud-Clone |
1x48-wells test plate |
EUR 552.76 |
|
|
|
Description: This is Competitive Enzyme-linked immunosorbent assay for Antibody Detection.detection of Human Anti-Anti-Sperm Antibody Antibody (Anti-AsAb) in serum, plasma and other biological fluids. |
Human Anti-Anti-Sperm Antibody Antibody (Anti-AsAb) ELISA Kit |
|
AEA465Hu-1x96wellstestplate |
Cloud-Clone |
1x96-wells test plate |
EUR 746.8 |
|
|
|
Description: This is Competitive Enzyme-linked immunosorbent assay for Antibody Detection.detection of Human Anti-Anti-Sperm Antibody Antibody (Anti-AsAb) in serum, plasma and other biological fluids. |
Human Anti-Anti-Sperm Antibody Antibody (Anti-AsAb) ELISA Kit |
|
AEA465Hu-5x96wellstestplate |
Cloud-Clone |
5x96-wells test plate |
EUR 3060.6 |
|
|
|
Description: This is Competitive Enzyme-linked immunosorbent assay for Antibody Detection.detection of Human Anti-Anti-Sperm Antibody Antibody (Anti-AsAb) in serum, plasma and other biological fluids. |
Human Anti-Anti-Sperm Antibody Antibody (Anti-AsAb) ELISA Kit |
|
4-AEA465Hu |
Cloud-Clone |
-
EUR 5698.00
-
EUR 3011.00
-
EUR 747.00
|
-
10 plates of 96 wells
-
5 plates of 96 wells
-
1 plate of 96 wells
|
|
|
|
Description: Enzyme-linked immunosorbent assay based on the Competitive Inhibition method for detection of Human Anti-Anti-Sperm Antibody Antibody (Anti-AsAb) in samples from serum, plasma and other biological fluids with no significant corss-reactivity with analogues from other species. |
) ELISA kit for Human Anti-AsAb (Anti-Anti-Sperm Antibody Antibody) |
|
ELK8071 |
ELK Biotech |
1 plate of 96 wells |
EUR 432 |
|
|
|
Description: A competitive Inhibition ELISA kit for detection of Anti-Anti-Sperm Antibody Antibody from Human in samples from blood, serum, plasma, cell culture fluid and other biological fluids. |
 Anti-MeCP2 Antibody |
|
M00047-1 |
BosterBio |
100ul |
EUR 397 |
|
Description: Rabbit Polyclonal MeCP2 Antibody. Validated in IHC, WB and tested in Human, Monkey, Mouse, Rat. |
 Anti-GAPDH Antibody |
|
M00227-4 |
BosterBio |
100ul |
EUR 397 |
|
Description: Rabbit Polyclonal GAPDH Antibody. Validated in IF, IHC, WB and tested in Bovine, Chicken, Equine, Human, Mouse, Pig, Rat. |
 Anti-Vimentin Antibody |
|
M00235-4 |
BosterBio |
100ul |
EUR 397 |
|
Description: Rabbit Polyclonal Vimentin Antibody. Validated in IHC, WB and tested in Bovine, Equine, Human, Mouse, Pig, Rat. |
Anti-Vimentin Antibody |
|
M00235-5 |
BosterBio |
100ul |
EUR 397 |
|
Description: Chicken Polyclonal Vimentin Antibody. Validated in IHC, WB and tested in Bovine, Chicken, Equine, Human, Mouse, Pig, Rat. |
 Anti-CNP Antibody |
|
M01017-2 |
BosterBio |
100ul |
EUR 397 |
|
Description: Rabbit Polyclonal CNP Antibody. Validated in IF, IHC, WB and tested in Human, Mouse, Rat. |
Anti-CNP Antibody |
|
M01017-3 |
BosterBio |
100ul |
EUR 397 |
|
Description: Chicken Polyclonal CNP Antibody. Validated in IHC, WB and tested in Equine, Pig. |
 Anti-GAP43 Antibody |
|
M01868-3 |
BosterBio |
100ul |
EUR 397 |
|
Description: Rabbit Polyclonal GAP43 Antibody. Validated in IF, IHC, WB and tested in Bovine, Chicken, Equine, Human, Mouse, Pig, Rat. |
Anti-GAP43 Antibody |
|
M01868-4 |
BosterBio |
100ul |
EUR 397 |
|
Description: Chicken Polyclonal GAP43 Antibody. Validated in IF, IHC, WB and tested in Bovine, Chicken, Equine, Human, Mouse, Pig, Rat. |
 Anti-GPSN2 Antibody |
|
F08289-1 |
BosterBio |
100ul |
EUR 397 |
|
Description: Rabbit Polyclonal Antibody for GPSN2 Antibody (TECR) detection.tested for WB in Human, Mouse, Rat. |
 Anti-Calbindin Antibody |
|
M03047-2 |
BosterBio |
100ul |
EUR 397 |
|
Description: Chicken Polyclonal Calbindin Antibody. Validated in IF, IHC, WB and tested in Bovine, Human, Mouse, Rat. |
 Anti-Fibrillarin Antibody |
|
M03178-4 |
BosterBio |
100ul |
EUR 397 |
|
Description: Rabbit Polyclonal Fibrillarin Antibody. Validated in IP, IHC, WB and tested in Human, Mouse, Rat. |
Anti-Fibrillarin Antibody |
|
M03178-5 |
BosterBio |
100ul |
EUR 397 |
|
Description: Chicken Polyclonal Fibrillarin Antibody. Validated in IF, IHC, WB and tested in Bovine, Chicken, Equine, Human, Mouse, Pig, Rat. |
 Anti-Parvalbumin Antibody |
|
M04041-2 |
BosterBio |
100ul |
EUR 397 |
|
Description: Chicken Polyclonal Parvalbumin Antibody. Validated in IHC, WB and tested in Human, Mouse, Rat. |
 Anti-Calretinin Antibody |
|
M04255-3 |
BosterBio |
100ul |
EUR 397 |
|
Description: Rabbit Polyclonal Calretinin Antibody. Validated in IF, IHC, WB and tested in Human, Mouse, Rat. |
Anti-Calretinin Antibody |
|
M04255-4 |
BosterBio |
100ul |
EUR 397 |
|
Description: Chicken Polyclonal Calretinin Antibody. Validated in IF, IHC, WB and tested in Bovine, Equine, Human, Mouse, Pig, Rat. |
 Anti-Laminin Antibody |
|
M04965 |
BosterBio |
100ul |
EUR 397 |
|
Description: Rabbit Polyclonal Laminin Antibody. Validated in IHC and tested in Human, Mouse, Rat. |
 Anti-Secretagogin Antibody |
|
M10629-1 |
BosterBio |
100ul |
EUR 397 |
|
Description: Rabbit Polyclonal Secretagogin Antibody. Validated in IHC, WB and tested in Human, Mouse, Rat. |
Anti-Secretagogin Antibody |
|
M10629-2 |
BosterBio |
100ul |
EUR 397 |
|
Description: Chicken Polyclonal Secretagogin Antibody. Validated in IF, IHC, WB and tested in Bovine, Human, Mouse, Rat. |
 Anti-ATF6 Antibody |
|
PA1011 |
BosterBio |
100ug/vial |
EUR 334 |
Anti-ATF6 Antibody |
|
PA1011-1 |
BosterBio |
100ug/vial |
EUR 294 |
 Anti-ATP5J Antibody |
|
PA1012 |
BosterBio |
100ug/vial |
EUR 294 |
 Anti-Bax Antibody |
|
PA1013 |
BosterBio |
100ug/vial |
EUR 294 |
Anti-Bax Antibody |
|
PA1013-1 |
BosterBio |
100ug/vial |
EUR 294 |
 Anti-BDNF Antibody |
|
PA1014 |
BosterBio |
100ug/vial |
EUR 294 |
 Anti-CCR5 Antibody |
|
PA1016 |
BosterBio |
100ug/vial |
EUR 294 |
Anti-CCR5 Antibody |
|
PA1016-1 |
BosterBio |
100ug/vial |
EUR 294 |
Anti-CCR5 Antibody |
|
PA1016-2 |
BosterBio |
100ug/vial |
EUR 294 |
 Anti-CCR7 Antibody |
|
PA1017 |
BosterBio |
100ug/vial |
EUR 294 |
 Anti-CD22 Antibody |
|
PA1018 |
BosterBio |
100ug/vial |
EUR 334 |
Anti-CD22 Antibody |
|
PA1018-1 |
BosterBio |
100ug/vial |
EUR 334 |
 Anti-CD40 Antibody |
|
PA1019 |
BosterBio |
100ug/vial |
EUR 294 |
Anti-CD40 Antibody |
|
PA1019-1 |
BosterBio |
100ug/vial |
EUR 294 |
 Anti-CD44 Antibody |
|
PA1021 |
BosterBio |
100ug/vial |
EUR 334 |
Anti-CD44 Antibody |
|
PA1021-1 |
BosterBio |
100ug/vial |
EUR 334 |
Anti-CD44 Antibody |
|
PA1021-2 |
BosterBio |
100ug/vial |
EUR 334 |
 Anti-GJB2 Antibody |
|
PA1025 |
BosterBio |
100ug/vial |
EUR 294 |
 Anti-CXCR2 Antibody |
|
PA1029 |
BosterBio |
100ug/vial |
EUR 294 |
 Anti-dUTPase Antibody |
|
PA1030 |
BosterBio |
100ug/vial |
EUR 334 |
 Anti-DUT Antibody |
|
PA1030-1 |
BosterBio |
100ug/vial |
EUR 334 |
 Anti-FGF2 Antibody |
|
PA1032 |
BosterBio |
100ug/vial |
EUR 334 |
 Anti-FGF4 Antibody |
|
PA1033 |
BosterBio |
100ug/vial |
EUR 294 |
Anti-GAP43 Antibody |
|
PA1037 |
BosterBio |
100ug/vial |
EUR 334 |
 Anti-Glast Antibody |
|
PA1038 |
BosterBio |
100ug/vial |
EUR 294 |
 Anti-GLUT4 Antibody |
|
PA1039 |
BosterBio |
100ug/vial |
EUR 334 |
 Anti-HMGB4 Antibody |
|
PA1042 |
BosterBio |
100ug/vial |
EUR 294 |
 Anti-INSL3 Antibody |
|
PA1044 |
BosterBio |
100ug/vial |
EUR 334 |
 Anti-KCA3.1 Antibody |
|
PA1047 |
BosterBio |
100ug/vial |
EUR 334 |
 Anti-KCNN4 Antibody |
|
PA1047-1 |
BosterBio |
100ug/vial |
EUR 294 |
 Anti-MIF Antibody |
|
PA1052 |
BosterBio |
100ug/vial |
EUR 334 |
