PEX26 polyclonal antibody
产品名称： PEX26 polyclonal antibody
英文名称： PEX26 polyclonal antibody
产品编号： PAB18622
产品价格： null
产品产地： 台湾
品牌商标： Abnova
更新时间： null
使用范围：
亚诺法生技股份有限公司（Abnova)
- 联系人 :
- 地址 : 台湾台北市内湖区洲子街 108 号 9 楼
- 邮编 : 11493
- 所在区域 : 台湾
- 电话 : +886-920**1152 点击查看
- 传真 : 点击查看
- 邮箱 : sales@abnova.com.tw
- Specification
- Product Description:
- Goat polyclonal antibody raised against synthetic peptide of PEX26.
- Immunogen:
- A synthetic peptide corresponding to amino acids at internal region of human PEX26.
- Sequence:
- C-QKPNLEGSVSHK
- Host:
- Goat
- Theoretical MW (kDa):
- 33
- Reactivity:
- Human
- Specificity:
- Reported variants represent identical protein: NP_060399.1, NP_001121121.1.
- Form:
- Liquid
- Purification:
- Antigen affinity purification
- Concentration:
- 0.5 mg/mL
- Storage Buffer:
- In 0.5 mg/mL Tris saline, pH 7.3 (0.02% sodium azide, 0.5% BSA)
- Storage Instruction:
- Store at -20°C.
Aliquot to avoid repeated freezing and thawing.
- Recommend Usage:
- ELISA (1:64000)
Western Blot (0.5-1.5 ug/mL)
The optimal working dilution should be determined by the end user.
- Note:
- This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Entrez GeneID:
- 55670
- Protein Accession#:
- NP_060399.1
- Gene Name:
- PEX26
- Gene Alias:
- FLJ20695,PEX26M1T,Pex26pM1T
- Gene Description:
- peroxisomal biogenesis factor 26
- Gene Ontology:
- Hyperlink
- Gene Summary:
- 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). Two transcript variants encoding the same protein have been identified for this gene. [provided by RefSeq
- Other Designations:
- OTTHUMP00000195598,peroxin-26,peroxisome assembly protein 26,peroxisome biogenesis disorder, complementation group 8,peroxisome biogenesis disorder, complementation group A,peroxisome biogenesis factor 26