LRRC47 抗体 (AA 309-583)
This 兔 多克隆 antibody specifically detects LRRC47 in WB, ELISA 和 FACS. It exhibits reactivity toward 人.
产品编号 ABIN7873742
发货至:
中国
Contact our Customer Service for availability and price in your country.
Contact Info
Our Local Distributor
中国
北京 101111
北京 101111
No. 88 KeChuang 6th Street
Beijing Economic Technological Development Area
Room 801-803
Quick Overview for LRRC47 抗体 (AA 309-583) (ABIN7873742)
抗原
LRRC47
(Leucine Rich Repeat Containing 47 (LRRC47))
适用
人
宿主
兔
克隆类型
多克隆
标记
This LRRC47 antibody is un-conjugated
应用范围
Western Blotting (WB), ELISA, Flow Cytometry (FACS)
-
-
抗原表位
- AA 309-583
-
原理
- LRRC47 Antibody / Leucine-rich repeat-containing protein 47
-
纯化方法
- Antigen affinity purified
-
免疫原
- An E.coli-derived human recombinant protein (amino acids L309-R583) was used as the immunogen for the LRRC47 antibody.
-
亚型
- IgG
-
-
anti-Leucine Rich Repeat Containing 47 (LRRC47) (AA 533-583) antibody
LRRC47 适用: 人, 小鼠 WB, IP 宿主: 兔 Polyclonal unconjugated
-
-
应用备注
- Optimal dilution of the LRRC47 antibody should be determined by the researcher.
-
限制
- 仅限研究用
-
-
-
状态
- Lyophilized
-
缓冲液
- 0.5 mg/mL if reconstituted with 0.2 mL sterile DI water
-
储存条件
- 4 °C,-20 °C
-
储存方法
- After reconstitution, the LRRC47 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
-
-
- LRRC47 (Leucine Rich Repeat Containing 47 (LRRC47))
-
别名
- LRRC47
-
背景
- Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8 % of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes Lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma.
-
UniProt
- Q8N1G4
抗原
-
You are here:
