CAMPATH-1 Antigen (CD52) Antibody (FITC)

Este producto es parte de CD52 - CD52 molecule
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364€ (100 tests)

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935106861
info@markelab.com
name
CAMPATH-1 Antigen (CD52) Antibody (FITC)
category
Primary Antibodies
provider
Abbexa
reference
abx347165
tested applications
FCM

Description

CAMPATH-1 Antigen (CD52) Antibody is a Mouse Monoclonal Antibody against CAMPATH-1 Antigen (CD52).

Documents del producto

Instrucciones
Data sheet
Descargar

Product specifications

Category
Primary Antibodies
Immunogen Target
CAMPATH-1 Antigen (CD52)
Host
Mouse
Reactivity
Human
Recommended Dilution
Optimal dilutions/cocentrations should be determined by the end user.
Clonality
Monoclonal
Conjugation
FITC
Isotype
IgG3
Clone ID
A715
Size 1
100 tests
Tested Applications
FCM
Buffer
Stabilizing PBS solution containing 15 mM sodium azide.
Availability
Shipped within 5-12 working days.
Storage
Store in the dark at 2-8°C. Do not freeze. Avoid exposure to light.
Dry Ice
No
UniProt ID
P31358
Gene ID
1043
Alias
HE5,CDW52,EDDM5,CAMPATH-1 antigen,Cambridge pathology 1,Epididymal secretory protein E5,Human epididymis-specific protein 5
Background
Antibody anti-CD52
Status
RUO

Descripción

CD52 is a small glycoprotein predominantly expressed on the surface of mature lymphocytes (both T and B cells), monocytes, macrophages, eosinophils, and some epithelial cells of the reproductive system. The CD52 molecule plays an important role in regulating immune cell function, and its high expression on lymphocytes makes it a valuable therapeutic target in immunology and oncology, particularly in treatments for autoimmune diseases and certain types of leukemia, such as chronic lymphocytic leukemia (CLL). The precise function of CD52 remains somewhat unclear, although it is believed to be involved in modulating immune responses and cellular interactions. CD52 is the target of the monoclonal antibody alemtuzumab, a treatment used in autoimmune conditions like multiple sclerosis (MS) and certain cancers like CLL. Alemtuzumab binds to CD52 on the surface of immune cells and triggers their destruction through immune-mediated mechanisms, leading to immunosuppression. This therapeutic aspect has drawn attention to the biological and clinical significance of the CD52 molecule.

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