TEL: +86 571 56623320    EMAIL: [email protected]

Rabbit Anti-LRIT3 antibody
Rabbit Anti-LRIT3 antibody
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;
Total
(Vip priceV)
Regular members: $334.4
View History [Clear]

Details

Product Name LRIT3
Chinese Name LRIT3蛋白抗体
Alias 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
Research Area Cell biology  immunology  
Immunogen Species Rabbit
Clonality Polyclonal
React Species (predicted: Human, )
Applications ELISA=1:5000-10000 IHC-P=1:100-500 IHC-F=1:100-500 ICC=1:100-500 IF=1:100-500 (Paraffin sections need antigen repair)
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
Theoretical molecular weight 73kDa
Cellular localization The cell membrane 
Form Liquid
Concentration 1mg/ml
immunogen KLH conjugated synthetic peptide derived from human FLJ44691: 401-500/679 
Lsotype IgG
Purification affinity purified by Protein A
Buffer Solution 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
Storage Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
Attention This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
Product Detail 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



References (0)

No References

Bought notes(bought amounts latest0)

No one bought this product
Total 0 records, divided into1 pages First Prev Next Last

User Comment(Total0User Comment Num)

  • No comment
Total 0 records, divided into1 pages First Prev Next Last
Username: Anonymous user
E-mail:
Rank:
Content:
Verification code: captcha

Call us

+86 571 56623320

Address

Room 1-315, Kongle Changqing Building, No. 160 Guangye Road,Gongshu District, Hangzhou City, Zhejiang Province, China

Join Us with

Leave a message
* To protect against spam, please pass the CAPTCHA test below.