CLDN19 (Human) Recombinant Protein (Q01)
产品名称： CLDN19 (Human) Recombinant Protein (Q01)
英文名称： CLDN19 (Human) Recombinant Protein (Q01)
产品编号： H00149461-Q01
产品价格： 0
产品产地： 台湾
品牌商标： Abnova
更新时间： null
使用范围： null
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:
- Human CLDN19 partial ORF ( NP_683763.1, 29 a.a. - 81 a.a.) recombinant protein with GST-tag at N-terminal.
- Sequence:
- QWKQSSYAGDAIITAVGPYEGLWMSCASQSTGQVQCKLYDSLLALDGHIQSAR
- Theoretical MW (kDa):
- 31.57
- Preparation Method:
- in vitro wheat germ expression system
- Purification:
- Glutathione Sepharose 4 Fast Flow
- Storage Buffer:
- 50 mM Tris-HCI, 10 mM reduced Glutathione, pH=8.0 in the elution buffer.
- Storage Instruction:
- Store at -80°C. Aliquot to avoid repeated freezing and thawing.
- Quality Control Testing:
- 12.5% SDS-PAGE Stained with Coomassie Blue.
- Note:
- Best use within three months from the date of receipt of this protein.
- MSDS:
Download
- Application Image
- Enzyme-linked Immunoabsorbent Assay
- Western Blot (Recombinant protein)
- Antibody Production
- Protein Array
- Entrez GeneID:
- 149461
- GeneBank Accession#:
- NM_148960
- Protein Accession#:
- NP_683763.1
- Gene Name:
- CLDN19
- Gene Alias:
- -
- Gene Description:
- claudin 19
- Gene Ontology:
- Hyperlink
- Gene Summary:
- The product of this gene belongs to the claudin family. It plays a major role in tight junction-specific obliteration of the intercellular space, through calcium-independent cell-adhesion activity. Defects in this gene are the cause of hypomagnesemia renal with ocular involvement (HOMGO). HOMGO is a progressive renal disease characterized by primary renal magnesium wasting with hypomagnesemia, hypercalciuria and nephrocalcinosis associated with severe ocular abnormalities such as bilateral chorioretinal scars, macular colobomata, significant myopia and nystagmus. Two transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq
- Other Designations:
- OTTHUMP00000008733