Peroxisomal Biogenesis Factor 26 (PEX26) (Middle Region) Peptide
PEX26
适用: 人
宿主: 合成
BP, WB
产品编号 ABIN5513718
发货至:
中国
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Contact Info
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Quick Overview for Peroxisomal Biogenesis Factor 26 (PEX26) (Middle Region) Peptide (ABIN5513718)
抗原
PEX26
(Peroxisomal Biogenesis Factor 26 (PEX26))
宿主
人
资源
合成
应用范围
Blocking Peptide (BP), Western Blotting (WB)
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蛋白结构域
- Middle Region
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序列
- AIHTARQQQK QEHSGSEEAQ KPNLEGSVSH KFLSLPMLVR QLWDSAVSHF
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产品特性
- This is a synthetic peptide designed for use in combination with anti- PEX26 Antibody. It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
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应用备注
- Optimal working dilution should be determined by the investigator.
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限制
- 仅限研究用
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状态
- Lyophilized
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溶解方式
- Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
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储存条件
- -20 °C
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储存方法
- For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
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- PEX26 (Peroxisomal Biogenesis Factor 26 (PEX26))
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背景
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This gene belongs to the peroxin-26 gene family. It is probably required for protein import into peroxisomes. It anchors PEX1 and PEX6 to peroxisome membranes, possibly to form heteromeric AAA ATPase complexes required for the import of proteins into peroxisomes. Defects in this gene are the cause of peroxisome biogenesis disorder complementation group 8 (PBD-CG8). PBD refers to a group of peroxisomal disorders arising from a failure of protein import into the peroxisomal membrane or matrix. The PBD group is comprised of four disorders: Zellweger syndrome (ZWS), neonatal adrenoleukodystrophy (NALD), infantile Refsum disease (IRD), and classical rhizomelic chondrodysplasia punctata (RCDP). Alternatively spliced transcript variants have been identified for this gene.
Alias Symbols: PBD7A, PBD7B, PEX26M1T, Pex26pM1T
Protein Size: 305 -
基因ID
- 55670
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NCBI登录号
- NM_001127649, NP_001121121
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UniProt
- Q7Z412
抗原
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