TRIM37 polyclonal antibody
产品名称： TRIM37 polyclonal antibody
英文名称： TRIM37 polyclonal antibody
产品编号： PAB6245
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 TRIM37.
- Immunogen:
- A synthetic peptide corresponding to human TRIM37.
- Sequence:
- C-EDLSFNTDENSGR
- Host:
- Goat
- Theoretical MW (kDa):
- 111
- Form:
- Liquid
- Purification:
- Antigen affinity purification
- Concentration:
- 0.5 mg/mL
- Storage Buffer:
- In Tris saline, pH 7.3 (0.5% BSA, 0.02% sodium azide)
- Storage Instruction:
- Store at -20°C.
Aliquot to avoid repeated freezing and thawing.
- Quality Control Testing:
- Antibody Reactive Against Synthetic Peptide.
- Recommend Usage:
- ELISA (1:64000)
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.
- Publication Reference
- 1.
- Gene encoding a new RING-B-box-Coiled-coil protein is mutated in mulibrey nanism.
Avela K, Lipsanen-Nyman M, Idanheimo N, Seemanova E, Rosengren S, Makela TP, Perheentupa J, Chapelle AD, Lehesjoki AE.Nat Genet. 2000 Jul;25(3):298-301.
- Application Image
- ELISA
- Entrez GeneID:
- 4591
- Protein Accession#:
- NP_056109
- Gene Name:
- TRIM37
- Gene Alias:
- KIAA0898,MUL,POB1,TEF3
- Gene Description:
- tripartite motif-containing 37
- Gene Ontology:
- Hyperlink
- Gene Summary:
- This gene encodes a member of the tripartite motif (TRIM) family, whose members are involved in diverse cellular functions such as developmental patterning and oncogenesis. The TRIM motif includes zinc-binding domains, a RING finger region, a B-box motif and a coiled-coil domain. The RING finger and B-box domains chelate zinc and might be involved in protein-protein and/or protein-nucleic acid interactions. The gene mutations are associated with mulibrey (muscle-liver-brain-eye) nanism, an autosomal recessive disorder that involves several tissues of mesodermal origin. Alternatively spliced transcript variants encoding the same protein have been identified. [provided by RefSeq
- Other Designations:
- RING-B-box-coiled-coil protein,tripartite motif-containing 37 protein
- Gene Pathway