PEX3 purified MaxPab mouse polyclonal antibody (B01P)
产品名称： PEX3 purified MaxPab mouse polyclonal antibody (B01P)
英文名称： PEX3 purified MaxPab mouse polyclonal antibody (B01P)
产品编号： H00008504-B01P
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:
- Mouse polyclonal antibody raised against a full-length human PEX3 protein.
- Immunogen:
- PEX3 (NP_003621.1, 1 a.a. ~ 373 a.a) full-length human protein.
- Sequence:
- MLRSVWNFLKRHKKKCIFLGTVLGGVYILGKYGQKKIREIQEREAAEYIAQARRQYHFESNQRTCNMTVLSMLPTLREALMQQLNSESLTALLKNRPSNKLEIWEDLKIISFTRSTVAVYSTCMLVVLLRVQLNIIGGYIYLDNAAVGKNGTTILAPPDVQQQYLSSIQHLLGDGLTELITVIKQAVQKVLGSVSLKHSLSLLDLEQKLKEIRNLVEQHKSSSWINKDGSKPLLCHYMMPDEETPLAVQACGLSPRDITTIKLLNETRDMLESPDFSTVLNTCLNRGFSRLLDNMAEFFRPTEQDLQHGNSMNSLSSVSLPLAKIIPIVNGQIHSVCSETPSHFVQDLLTMEQVKDFAANVYEAFSTPQQLEK
- Host:
- Mouse
- Reactivity:
- Human
- Storage Buffer:
- In 1x PBS, pH 7.2
- Storage Instruction:
- Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.
- Quality Control Testing:
- Antibody reactive against mammalian transfected lysate.
- MSDS:
Download
- Applications
- Western Blot (Transfected lysate)
- Western Blot analysis of PEX3 expression in transfected 293T cell line (H00008504-T01) by PEX3 MaxPab polyclonal antibody.
Lane 1: PEX3 transfected lysate(41.03 KDa).
Lane 2: Non-transfected lysate. - Protocol Download
- Entrez GeneID:
- 8504
- GeneBank Accession#:
- NM_003630.1
- Protein Accession#:
- NP_003621.1
- Gene Name:
- PEX3
- Gene Alias:
- DKFZp686N14184,FLJ13531,TRG18
- Gene Description:
- peroxisomal biogenesis factor 3
- Gene Ontology:
- Hyperlink
- Gene Summary:
- The product of this gene is involved in peroxisome biosynthesis and integrity. It assembles membrane vesicles before the matrix proteins are translocated. 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
- Other Designations:
- OTTHUMP00000017334,OTTHUMP00000040175,peroxin-3,peroxisomal assembly protein PEX3,transformation-related protein 18