MOUSE SPLEEN TOTAL PROTEIN LYSATE (7 DAYS OLD), Product Type Cell Lysate, Specificity SPLEEN LYSATE , Target Species Mouse, Host N_A, Format Total Protein Lysate, Isotypes , Applications WB, Cl
- Known as:
- MOUSE SPLEEN TOTAL PROTEIN LYSATE (7 DAYS OLD), Product Type Cell Lysate, Specificity SPLEEN LYSATE , Target Species Mouse, Host N_A, Format Total Protein Lysate, Isotypes , Applications Western Blot, Cl
- Catalog number:
- LYS168
- Product Quantity:
- 0.1 mg
- Category:
- -
- Supplier:
- AbD
- Gene target:
- MOUSE SPLEEN TOTAL PROTEIN LYSATE (7 DAYS OLD) Product Type Cell Lysate Specificity Target Species Mouse Host N_A Format Total Protein Isotypes Applications
Related genes to: MOUSE SPLEEN TOTAL PROTEIN LYSATE (7 DAYS OLD), Product Type Cell Lysate, Specificity SPLEEN LYSATE , Target Species Mouse, Host N_A, Format Total Protein Lysate, Isotypes , Applications WB, Cl
- Gene:
- KCTD13 NIH gene
- Name:
- potassium channel tetramerization domain containing 13
- Previous symbol:
- -
- Synonyms:
- PDIP1, FKSG86, POLDIP1
- Chromosome:
- 16p11.2
- Locus Type:
- gene with protein product
- Date approved:
- 2003-11-24
- Date modifiied:
- 2014-11-19
- Gene:
- PNPT1 NIH gene
- Name:
- polyribonucleotide nucleotidyltransferase 1
- Previous symbol:
- DFNB70
- Synonyms:
- PNPase, OLD35, old-35
- Chromosome:
- 2p16.1
- Locus Type:
- gene with protein product
- Date approved:
- 2003-09-25
- Date modifiied:
- 2016-10-05
- Gene:
- POLD1 NIH gene
- Name:
- DNA polymerase delta 1, catalytic subunit
- Previous symbol:
- POLD
- Synonyms:
- CDC2
- Chromosome:
- 19q13.3
- Locus Type:
- gene with protein product
- Date approved:
- 1992-02-06
- Date modifiied:
- 2019-04-23
- Gene:
- POLD4 NIH gene
- Name:
- DNA polymerase delta 4, accessory subunit
- Previous symbol:
- -
- Synonyms:
- p12, POLDS
- Chromosome:
- 11q13.2
- Locus Type:
- gene with protein product
- Date approved:
- 2000-12-04
- Date modifiied:
- 2016-10-05
- Gene:
- TYRP1 NIH gene
- Name:
- tyrosinase related protein 1
- Previous symbol:
- TYRP, CAS2
- Synonyms:
- GP75, CATB, TRP, b-PROTEIN, OCA3
- Chromosome:
- 9p23
- Locus Type:
- gene with protein product
- Date approved:
- 1991-09-04
- Date modifiied:
- 2016-04-19
Related products to: MOUSE SPLEEN TOTAL PROTEIN LYSATE (7 DAYS OLD), Product Type Cell Lysate, Specificity SPLEEN LYSATE , Target Species Mouse, Host N_A, Format Total Protein Lysate, Isotypes , Applications WB, Cl
Related articles to: MOUSE SPLEEN TOTAL PROTEIN LYSATE (7 DAYS OLD), Product Type Cell Lysate, Specificity SPLEEN LYSATE , Target Species Mouse, Host N_A, Format Total Protein Lysate, Isotypes , Applications WB, Cl
- Vitiligo is a common autoimmune skin disease. Capsaicin has been found to exert a positive effect on vitiligo treatment, and mesenchymal stem cells (MSCs) are also confirmed to be an ideal cell type. This study aimed to explore the influence of capsaicin combined with stem cells on the treatment of vitiligo and to confirm the molecular mechanism of capsaicin combined with stem cells in treating vitiligo. - Source: PubMed
Publication date: 2024/05/11
Wu YifeiWang XiaochuanZhang JiayuDu ShaWang ZhiqiongLi JinrongZhang WenheXiang JieLi RenfuLiu JingBi Xin - Avian feather color is a fascinating trait, and the genetic mechanism of duck plumage formation is still in the preliminary stage. In this study, feather color of Liancheng White ducks was analyzed by determination of melanin content and RNA-seq analysis. In this research, 9 ducks from Mallards (n = 3), Liancheng White (n = 3) and Pekin ducks (n = 3) were used by high performance liquid chromatography (HPLC) and Masson-Fontana staining to reveal the difference of feather melanin content. RNA-seq from 11 hair follicle tissues (1- and 8-wk-old) of Liancheng White ducks (n = 5) and Pekin ducks (n = 7) was used to analyze the candidate genes for the feather melanin synthesis, and Immunofluorescence experiment was used to show the protein expression in 6 black- and white-feathered ducks. Pectorale, skin, liver, fat, brain, heart, kidney, lung, spleen of an 8-wk-old black-feathered Mallard were collected for candidate gene expression. The results showed that the contents of feathers, beak, web melanin in Liancheng White ducks were higher than in Pekin ducks (p < 0.05). Melanin within hair follicles was located in the barb ridge and hair matrix of black feather duck, also we found that TYRP1, TYR, SOX10 genes were differentially expressed between Liancheng White and Pekin ducks (p < 0.05), and these genes were mainly expressed showed in duck skin tissues. This study revealed the unique feather color phenotype of Liancheng White duck shedding light on the transcriptome that underlies it. - Source: PubMed
Publication date: 2024/04/24
Wang ZhenGuo ZhanbaoMou QimingLiu HongfeiLiu DapengTang HeheHou ShuishengSchroyen MartineZhou Zhengkui - As modern humans ventured out of Africa and dispersed around the world, they faced novel environmental challenges that led to geographic adaptations including skin colour. Over the long history of human evolution, skin colour has changed dramatically, showing tremendous diversity across different geographical regions, for example, the majority of individuals from the expansive lands of Africa have darker skin, whereas the majority of people from Eurasia exhibit lighter skin. What adaptations did lighter skin confer upon modern humans as they migrated from Africa to Eurasia? What genetic mechanisms underlie the diversity of skin colour observed in different populations? In recent years, scientists have gradually gained a deeper understanding of the interactions between pigmentation gene and skin colour through population-based genomic studies of different groups around the world, particularly in East Asia and Africa. In this review, we summarize our current understanding of 26 skin colour-related pigmentation genes and 48 SNPs that influence skin colour. Important pigmentation genes across three major populations are described in detail: MFSD12, SLC24A5, PDPK1 and DDB1/CYB561A3/TMEM138 influence skin colour in African populations; OCA2, KITLG, SLC24A2, GNPAT and PAH are key to the evolution of skin pigmentation in East Asian populations; and SLC24A5, SLC45A2, TYR, TYRP1, ASIP, MC1R and IRF4 significantly contribute to the lightening of skin colour in European populations. We summarized recent findings in genomic studies of skin colour in populations that implicate diverse geographic environments, local adaptation among populations, gene flow and multi-gene interactions as factors influencing skin colour diversity. - Source: PubMed
Publication date: 2024/05/07
Liu JiumingBitsue Habtom KYang Zhaohui - The evolution of personalized medicine in dermatology signifies a transformative shift towards individualized treatments, driven by the integration of biomarkers. These molecular indicators serve beyond diagnostics, offering insights into disease staging, prognosis, and therapeutic monitoring. Specific criteria guide biomarker selection, ensuring attributes like specificity, sensitivity, cost feasibility, stability, rapid detection, and reproducibility. This literature review, based on data from PubMed, SCOPUS, and Web of Science, explores biomarkers in Hidradenitis Suppurativa (HS), Psoriasis, Atopic Dermatitis (AD), Alopecia Areata (AA), Vitiligo, and Chronic Spontaneous Urticaria (CSU). In HS, TNF-α, IL-1β, and MMPs serve as biomarkers, influencing targeted therapies like adalimumab and anakinra. Psoriasis involves biomarkers such as TNF-α, IL-23, and HLA genes, shaping treatments like IL23 and IL17 inhibitors. AD biomarkers include ECP, IL-4, IL-13, guiding therapies like dupilumab and tralokinumab. For AA, lipocalin-2, cytokines, and genetic polymorphisms inform JAK inhibitors' use. Vitiligo biomarkers range from cytokines to genetic markers like TYR, TYRP1, guiding treatments like JAK inhibitors. CSU biomarkers encompass IgE, cytokines, and autologous serum tests, influencing therapies like omalizumab and cyclosporine. Comparing conditions, common proinflammatory markers reveal limited specificity. While some biomarkers aid diagnosis and standard treatments, others hold more scientific than clinical value. Precision medicine, driven by biomarkers, has shown success in skin malignancies. Future directions involve AI-powered algorithms, nanotechnology, and multi-omics integration for personalized dermatological care. - Source: PubMed
Publication date: 2024/03/30
Tan Isabella JPodwojniak AliciaParikh AarushiCohen Bernard A - Exploration of gene expression variations is a potential source to unravel biological pathways involved in pathological changes in body and understand the mechanism underneath. Vitiligo patients were explored for gene expression changes transcriptionally at perilesional site in comparison to normal site of same patients for melanogenesis pathway (TYR, DCT & TYRP1) cell adhesion (MMPs & TIMP1), cell survival (BCL2 & BAX1) as well as proliferation, migration & development (SOX9, SOX10 & MITF) regulatory system, using skin biopsy samples. Results were also compared with changes in gene expression for melanocytes under stress after hydrogen peroxide treatment in-vitro. Gene amplification was carried out via real time PCR. We found increased expression of proliferation, migration & development regulatory genes as well as melanogenesis pathway genes at perilesional site of patients. In-vitro study also supports induced MITF expression and disturbed melanogenesis in melanocytes under stress. Expression level ratio of cell survival regulatory genes' (BCL2/BAX1) as well as cell adhesion regulatory genes (MMPs/TIMP1) was observed upregulated at patient's perilesional site however downregulated in hydrogen peroxide treated melanocytes in-vitro. Observed upregulated gene expression at perilesional site of patients may be via positive feedback loop in response to stress to increase cell tolerance power to survive against adverse conditions. Gene expression analysis suggests better cell survival and proliferation potential at perilesional site in vitiligo patients. It seems in-vivo conditions/growth factors supports cells to fight for survival to accommodate stressed conditions. - Source: PubMed
Publication date: 2024/04/25
Tanwar SushmaParsad Davinder