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LRIT3 Rabbit pAb (bs-16142R)  
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50ul/1180.00元
100ul/1980.00元
200ul/2800.00元
大包装/询价
产品编号 bs-16142R
英文名称 LRIT3 Rabbit pAb
中文名称 LRIT3蛋白抗体
别    名 CSNB1F; Fibronectin type III immunoglobulin and leucine rich repeat domains 4; FIGLER4; immunoglobulin-like domain and transmembrane domain-containing protein 3; Leucine rich repeat immunoglobulin like domain and transmembrane domain containing protein 3; Leucine-rich repeat; leucine-rich repeat, immunoglobulin like and transmembrane domains 3; LRIT3 protein; LRIT3_HUMAN; MGC120618,  FLJ44817
研究领域 细胞生物  免疫学  
抗体来源 Rabbit
克隆类型 Polyclonal
克 隆 号
交叉反应 (predicted: Human)
产品应用 IHC-P=1:100-500,IHC-F=1:100-500,IF=1:100-500,ICC/IF=1:100-500,ELISA=1:5000-10000
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理论分子量 73 kDa
检测分子量
细胞定位 细胞膜 
性    状 Liquid
浓    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human FLJ44691: 401-500/679 
亚    型
纯化方法 affinity purified by Protein A
缓 冲 液 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
保存条件 Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
注意事项 This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
产品介绍 This gene encodes a protein that has a fibronectin type III domain and a C-terminal transmembrane domain, as well as a leucine-rich repeat domain and immunoglobulin-like domain near the N-terminus. The encoded protein may regulate fibroblast growth factor receptors and affect the modification of these receptors, which are glycosylated differently in the Golgi and endoplasmic reticulum. Mutations in this gene are associated with congenital stationary night blindness, type 1F. [provided by RefSeq, May 2013]

Subcellular Location:
Membrane.

Similarity:
Contains 1 fibronectin type-III domain.
Contains 1 Ig-like (immunoglobulin-like) domain.
Contains 4 LRR (leucine-rich) repeats.
Contains 1 LRRCT domain.

SWISS:
Q3SXY7

Gene ID:
345193

Database links:

Entrez Gene: 345193 Human

Omim: 615004 Human

SwissProt: Q3SXY7 Human

Unigene: 308127 Human



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