Human VEGF R2 / KDR Protein, Strep Tag

Proteins and Peptides

貨號 Cat. No.
KDR-H5280
規格 Size
1mg
品牌 Brand
ACROBiosystems
Species
Human
Conjugate
Unconjugated
Expression System
HEK293
Tag
Strep Tag

Description




Source : 


Human VEGF R2, Strep Tag (KDR-H5280) is expressed from human 293 cells (HEK293). It contains AA Ala 20 - Glu 764 (Accession # AAI31823).


 

Molecule : VEGF R2


 

Synonyms : KDR,CD309,FLK1,VEGFR,VEGFR2


 

Format : Powder


 

Category : Bio-Markers & CD Antigens


 

Accession : AAI31823


 

Storage : -20℃


 

Shipping condition : Powder,RT


 

Molecular Weight : 86.3 kDa


 

Characteristics :


This protein carries a twin strep tag at the C-terminus. The protein has a calculated MW of 86.3 kDa. The protein migrates as 100-110 kDa under reducing (R) condition (SDS-PAGE) due to glycosylation.


 

Endotoxin Level : Less than 1.0 EU per μg by the LAL method.


 

Buffer : PBS, pH7.4


 

Description :


Kinase insert domain receptor (KDR) is also known as CD309, FLK1, VEGFR, VEGFR2, and is one of the subtypes of VEGFR. VEGF receptors are receptors for vascular endothelial growth factor (VEGF). There are three main subtypes of VEGFR, numbered 1, 2 and 3. The VEGF receptors have an extracellular portion consisting of 7 immunoglobulin-like domains, a single transmembrane spanning region and an intracellular portion containing a split tyrosine-kinase domain. VEGF-A binds to VEGFR-1 (Flt-1) and VEGFR-2 (KDR/Flk-1). VEGFR-2 appears to mediate almost all of the known cellular responses to VEGF.The function of VEGFR-1 is less well defined, although it is thought to modulate VEGFR-2 signaling. Another function of VEGFR-1 may be to act as a dummy/decoy receptor, sequestering VEGF from VEGFR-2 binding (this appears to be particularly important during vasculogenesis in the embryo). In addition, VEGFR2 is able to interact with HIV-1 extracellular Tat protein upon VEGF activation, and seems to enhance angiogenesis in Kaposi's sarcoma lesions.


 

References :


(1) Holmes K,et al., 2007, Cell Signal. 19 (10): 2003–2012.
(2) Stuttfeld E, et al., 2009, IUBMB Life 61 (9): 915–22.
(3) Fujita, N, et al., 2008, Biochemical and biophysical research communications 372 (2): 367–372.





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