Spark PLUS V450™ anti-mouse CD4 Antibody, CD4, RM4-5,BioLegend,100589

The RM4-5 antibody blocks the binding of GK1.5 antibody and H129.19 antibody to CD4+T cells, but not RM4-4 antibody. Additional reported applications (for the relevant formats) include: blocking of ligand binding,in vivodepletion of CD4+cells1, and immunohistochemistry of acetone-fixed frozen tissue sections2,3,11and paraffin-embedded sections11. Clone RM4-5 is not recommended for immunohistochemistry of formalin-fixed paraffin sections. Instead, acetone frozen or zinc-fixed paraffin sections are recommended. The Ultra-LEAF™ Purified antibody (Endotoxin < 0.01 EU/µg, Azide-Free, 0.2 µm filtered) is recommended for functional assays (Cat. No.100575 and 100576).

Host

Rat

Reactivity

Mouse

Application

FC - Quality tested

Platform ID

BAB210899393

BioLegend

Headquarters

8999 BioLegend Way San Diego, CA 92121 United States

Contact

Tel: 1-858-455-9588
Fax: +49 (4131) 7023913

Email:

Product Specifications
Scientific Background

Specifications

NameSpark PLUS V450™ anti-mouse CD4 Antibody, CD4, RM4-5
Cat. No.100589
HostRat
IsotypeRat IgG2a, κ
ReactivityMouse
ApplicationFC - Quality tested
ClonalityMonoclonal
Clone NumberRM4-5
Concentration0.2 mg/mL
TargetCD4
ImmunogenBALB/c mouse thymocytes
PurityThe antibody was purified by affinity chromatography and conjugated with Spark PLUS V450™ under optimal conditions.
FormulationPhosphate-buffered solution, pH 7.2, containing 0.09% sodium azide
StorageThe antibody solution should be stored undiluted between 2°C and 8°C, and protected from prolonged exposure to light.Do not freeze.
Regulatory StatusResearch Use Only

Scientific Background

CD4 is a 55 kD protein also known as L3T4 or T4. It is a member of the Ig superfamily, primarily expressed on most thymocytes and a subset of T cells, and weakly on macrophages and dendritic cells. It acts as a co-receptor with the TCR during T cell activation and thymic differentiation by binding MHC class II and associating with the protein tyrosine kinase lck.

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