PSMD12 Antibody
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货号:CSB-PA018902ESR2HU
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规格:¥440
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促销:
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图片:
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Western blot
All lanes: PSMD12antibody at 0.93μg/ml
Lane 1: U87 whole cell lysate
Lane 2: Hela whole cell lysate
Secondary
Goat polyclonal to rabbit IgG at 1/10000 dilution
Predicted band size: 53, 51 kDa
Observed band size: 53 kDa -
Immunohistochemistry of paraffin-embedded human gastric cancer using CSB-PA018902ESR2HU at dilution of 1:100
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其他:
产品详情
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产品名称:Rabbit anti-Homo sapiens (Human) PSMD12 Polyclonal antibody
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Uniprot No.:O00232
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基因名:PSMD12
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别名:26S proteasome non-ATPase regulatory subunit 12 antibody; 26S proteasome regulatory subunit p55 antibody; 26S proteasome regulatory subunit RPN5 antibody; MGC75406 antibody; p55 antibody; proteasome (prosome, macropain) 26S subunit, non ATPase12 antibody; Proteasome 26S non ATPase subunit 12 isoform 2 antibody; PSD12_HUMAN antibody; PSMD12 antibody; Rpn5 antibody
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宿主:Rabbit
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反应种属:Human
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免疫原:Recombinant Human 26S proteasome non-ATPase regulatory subunit 12 protein (197-456AA)
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免疫原种属:Homo sapiens (Human)
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标记方式:Non-conjugated
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克隆类型:Polyclonal
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抗体亚型:IgG
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纯化方式:Antigen Affinity Purified
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浓度:It differs from different batches. Please contact us to confirm it.
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保存缓冲液:PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
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产品提供形式:Liquid
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应用范围:ELISA, WB, IHC
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推荐稀释比:
Application Recommended Dilution WB 1:1000-1:5000 IHC 1:20-1:200 -
Protocols:
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储存条件:Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
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货期:Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.
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靶点详情
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功能:Component of the 26S proteasome, a multiprotein complex involved in the ATP-dependent degradation of ubiquitinated proteins. This complex plays a key role in the maintenance of protein homeostasis by removing misfolded or damaged proteins, which could impair cellular functions, and by removing proteins whose functions are no longer required. Therefore, the proteasome participates in numerous cellular processes, including cell cycle progression, apoptosis, or DNA damage repair.
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基因功能参考文献:
- we identified six de novo genomic deletions and four de novo point mutations in unrelated individuals with intellectual disability, congenital malformations, ophthalmologic anomalies, feeding difficulties, deafness, and subtle dysmorphic facial features PMID: 28132691
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相关疾病:Stankiewicz-Isidor syndrome (STISS)
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蛋白家族:Proteasome subunit p55 family
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数据库链接:
HGNC: 9557
OMIM: 604450
KEGG: hsa:5718
STRING: 9606.ENSP00000348442
UniGene: Hs.4295
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