Recombinant Human CD20 (C-6His-Flag)

Recombinant Human CD20 (C-6His-Flag)

Size1:10μg price1:$405
Size2:50μg price2:$1118
Size3:500μg price3:$5900
SKU: PHH2441 Category: Target Proteins Tags: ,

Datasheet

Name

Recombinant Human CD20 (C-6His-Flag)

Purity

Greater than 95% as determined by reducing SDS-PAGE

Endotoxin level

<1 EU/µg as determined by LAL test.

Construction

Recombinant Human B-lymphocyte antigen CD20 is produced by our Mammalian expression system and the target gene encoding Met1-Pro297 is expressed with a 6His, Flag tag at the C-terminus.The product is not recommended for cell based experiments.*The product is not recommended for cell based experiments.

Accession #

P11836

Host

Human cells

Species

Human

Predicted Molecular Mass

35.1 kDa

Buffer

Supplied as a 0.2 μm filtered solution of 50mM HEPES-Na, 150mM NaCl, 0.02%DDM, 0.004%CHS, 5%Glycerol, pH7.5.

Form

Liquid

Shipping

The product is shipped on dry ice/polar packs.Upon receipt, store it immediately at the temperature listed below.

Stability&Storage

Store at ≤-70°C, stable for 6 months after receipt.Store at ≤-70°C, stable for 3 months under sterile conditions after opening. Please minimize freeze-thaw cycles.

 

 

 

Alternative Names

B-lymphocyte antigen CD20; B-lymphocyte surface antigen B1; Leukocyte surface antigen Leu-16; Membrane-spanning 4-domains subfamily A member 1; Bp35; CD20; MS4A1

 

Background

CD20 is a 33-37 kDa non-glycosylated protein expressed on the surface of normal and malignant B lymphocytes, and belongs to the MS4A (membrane-spanning 4-domain family A) protein family. CD20 protein consists of four hydrophobic transmembrane domains, one intracellular and two extracellular domains (large and small loops) with both N- and C- termini residing within the cytosol. CD20 is also known to be physically coupled to major histocompatibility complex class II (MHCII), CD40 molecule, BCR, and the C-terminal src kinase-binding protein (CBP) that interacts with Src kinases such as LYN, FYN, and LCK. CD20 deficiency resulted in a reduced number of circulating memory B cells, reduced isotype switching of Ig, and decreased IgG antibody levels. In agreement with this observation, challenging the patient’s primary B cells in vitro using T-dependent and Tindependent antigens led to the normal proliferation and secretion of IgM but reduced production of IgG.

 

Note

For Research Use Only , Not for Diagnostic Use.