WBSCR18 purified MaxPab mouse polyclonal antibody (B01P)
产品名称： WBSCR18 purified MaxPab mouse polyclonal antibody (B01P)
英文名称： WBSCR18 purified MaxPab mouse polyclonal antibody (B01P)
产品编号： H00084277-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 WBSCR18 protein.
- Immunogen:
- WBSCR18 (AAH05056, 1 a.a. ~ 226 a.a) full-length human protein.
- Sequence:
- MAAMRWRWWQRLLPWRLLQARGFPQNSAPSLGLRARTYSQGDCSYSRTALYDLLGVPSTATQAQIKAAYYRQCFLYHPDRNSGSAEAAERFTRISQAYVVLGSATLRRKYDRGLLSDEDLRGPGVRPSRTPAPDPGSPRTPPPTSRTHDGSRASPGANRTMFNFDAFYQAHYGEQLERERRLRARREALRKRQEYRSMKGLRWEDTRDTAAIFLIFSIFIIIGFYI
- 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 DNAJC30 expression in transfected 293T cell line (H00084277-T01) by DNAJC30 MaxPab polyclonal antibody.
Lane 1: WBSCR18 transfected lysate(24.86 KDa).
Lane 2: Non-transfected lysate. - Protocol Download
- Entrez GeneID:
- 84277
- GeneBank Accession#:
- BC005056
- Protein Accession#:
- AAH05056
- Gene Name:
- DNAJC30
- Gene Alias:
- MGC12943,WBSCR18
- Gene Description:
- DnaJ (Hsp40) homolog, subfamily C, member 30
- Gene Ontology:
- Hyperlink
- Gene Summary:
- This intronless gene encodes a member of the DNAJ molecular chaperone homology domain-containing protein family. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. [provided by RefSeq
- Other Designations:
- DnaJ (Hsp40) homolog subfamily C member 30,OTTHUMP00000024908,OTTHUMP00000160500,Williams Beuren syndrome chromosome region 18