验证数据展示
经过测试的应用
Positive WB detected in | HEK-293 cells, mouse skeletal muscle tissue, HeLa cells, mouse testis tissue, L02 cells |
Positive IHC detected in | human colon cancer tissue Note: suggested antigen retrieval with TE buffer pH 9.0; (*) Alternatively, antigen retrieval may be performed with citrate buffer pH 6.0 |
Positive IF/ICC detected in | MCF-7 cells |
推荐稀释比
应用 | 推荐稀释比 |
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Western Blot (WB) | WB : 1:500-1:2000 |
Immunohistochemistry (IHC) | IHC : 1:50-1:500 |
Immunofluorescence (IF)/ICC | IF/ICC : 1:10-1:100 |
It is recommended that this reagent should be titrated in each testing system to obtain optimal results. | |
Sample-dependent, Check data in validation data gallery. |
产品信息
12195-1-AP targets VPS33B in WB, IHC, IF/ICC, IP, CoIP, ChIP, ELISA applications and shows reactivity with human, mouse, rat samples.
经测试应用 | WB, IHC, IF/ICC, ELISA Application Description |
文献引用应用 | WB, IHC, IF, IP, CoIP, ChIP |
经测试反应性 | human, mouse, rat |
文献引用反应性 | human, mouse, zebrafish |
免疫原 | VPS33B fusion protein Ag2833 种属同源性预测 |
宿主/亚型 | Rabbit / IgG |
抗体类别 | Polyclonal |
产品类型 | Antibody |
全称 | vacuolar protein sorting 33 homolog B (yeast) |
别名 | Vacuolar protein sorting-associated protein 33B, hVPS33B |
计算分子量 | 617 aa, 71 kDa |
观测分子量 | 65-71 kDa |
GenBank蛋白编号 | BC016445 |
基因名称 | VPS33B |
Gene ID (NCBI) | 26276 |
RRID | AB_2215198 |
偶联类型 | Unconjugated |
形式 | Liquid |
纯化方式 | Antigen affinity purification |
UNIPROT ID | Q9H267 |
储存缓冲液 | PBS with 0.02% sodium azide and 50% glycerol , pH 7.3 |
储存条件 | Store at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage. |
背景介绍
VPS33B, a homolog of yeast class C vacuolar protein sorting (vps) protein Vps33p, belongs to the STXBP/unc-18/SEC1 family. It may play a role in vesicle-mediated protein trafficking to lysosomal compartments and in membrane docking/fusion reactions of late endosomes/lysosomes. VPS33B mediates phagolysosomal fusion in macrophages (PMID: 18474358). Defects in VPS33B account for most cases of arthrogryposis-renal dysfunction-cholestasis (ARC) syndrome, which is a multisystem disorder associated with abnormalities in polarized liver and kidney cells (PMID: 20190753).
实验方案
Product Specific Protocols | |
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WB protocol for VPS33B antibody 12195-1-AP | Download protocol |
IHC protocol for VPS33B antibody 12195-1-AP | Download protocol |
IF protocol for VPS33B antibody 12195-1-AP | Download protocol |
Standard Protocols | |
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Click here to view our Standard Protocols |
发表文章
Species | Application | Title |
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Nat Genet Mutations in VIPAR cause an arthrogryposis, renal dysfunction and cholestasis syndrome phenotype with defects in epithelial polarization.
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Proc Natl Acad Sci U S A Mycobacterium tuberculosis protein tyrosine phosphatase (PtpA) excludes host vacuolar-H+-ATPase to inhibit phagosome acidification. | ||
J Cell Sci Late endosomal transport and tethering are coupled processes controlled by RILP and the cholesterol sensor ORP1L. | ||
Clin Kidney J Glomerular involvement in the arthrogryposis, renal dysfunction and cholestasis syndrome. | ||
Cancer Sci VPS33B interacts with NESG1 to suppress cell growth and cisplatin chemoresistance in ovarian cancer. |