PEX19 抗体
Quick Overview for PEX19 抗体 (ABIN7467211)
抗原
See all PEX19 抗体适用
宿主
克隆类型
标记
应用范围
克隆位点
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交叉反应
- 人, 大鼠
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纯化方法
- Affinity purified by Protein G.
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免疫原
- Recombinant protein encompassing a sequence within the center region of human PEX19. The exact sequence is proprietary.
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亚型
- IgG2b
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anti-Peroxisomal Biogenesis Factor 19 (PEX19) antibody
PEX19 适用: 人 WB, IF, ICC, IHC (p) 宿主: 兔 Polyclonal unconjugated
anti-Peroxisomal Biogenesis Factor 19 (PEX19) (AA 1-299) antibodyPEX19 适用: 人 WB, ELISA 宿主: 小鼠 Monoclonal 2E4 unconjugated
anti-Peroxisomal Biogenesis Factor 19 (PEX19) (AA 1-299) antibodyPEX19 适用: 人 WB, IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-Peroxisomal Biogenesis Factor 19 (PEX19) (AA 1-299) antibodyPEX19 适用: 人 ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-Peroxisomal Biogenesis Factor 19 (PEX19) (AA 1-299) antibodyPEX19 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
anti-Peroxisomal Biogenesis Factor 19 (PEX19) antibodyPEX19 适用: 人, 小鼠, 大鼠 IF 宿主: 兔 Polyclonal unconjugated
anti-Peroxisomal Biogenesis Factor 19 (PEX19) (C-Term) antibodyPEX19 适用: 人, 小鼠, 大鼠, 兔, 猴 WB 宿主: 兔 Polyclonal unconjugated
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应用备注
- WB: 1:500-1:3000. ICC/IF: 1:100-1:1000. FACS: 1:50-1:200. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.
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说明
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Positive Control: PC-12 , Rat-2 , Jurkat , Raji , K562 , THP-1 , NCI-H929
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限制
- 仅限研究用
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状态
- Liquid
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浓度
- 1.17 mg/mL
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缓冲液
- PBS, No Preservative
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储存液
- Without preservative
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储存条件
- 4 °C,-20 °C
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储存方法
- Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
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- PEX19 (Peroxisomal Biogenesis Factor 19 (PEX19))
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别名
- peroxisomal biogenesis factor 19
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背景
- Peroxisomal biogenesis factor 19 , D1S2223E , HK33 , PBD12A , PMP1 , PMPI , PXF , PXMP1,This gene is necessary for early peroxisomal biogenesis. It acts both as a cytosolic chaperone and as an import receptor for peroxisomal membrane proteins (PMPs). Peroxins (PEXs) are proteins that are essential for the assembly of functional peroxisomes. The peroxisome biogenesis disorders (PBDs) are a group of genetically heterogeneous autosomal recessive, lethal diseases characterized by multiple defects in peroxisome function. The peroxisomal biogenesis disorders are a heterogeneous group with at least 14 complementation groups and with more than 1 phenotype being observed in cases falling into particular complementation groups. Although the clinical features of PBD patients vary, cells from all PBD patients exhibit a defect in the import of one or more classes of peroxisomal matrix proteins into the organelle. Defects in this gene are a cause Zellweger syndrome (ZWS). [provided by RefSeq]
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分子量
- 33 kDa
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基因ID
- 5824
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UniProt
- P40855
抗原
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