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anti-S100A1, DyLight 680, Clone: 4C4.9, Novus Biologicals™

Manufacturer:  Novus BiologicalsSupplier Diversity Partner NBP233168FR

Catalog No. NBP233168FR

This item has been discontinued by the manufacturer and is no longer available. Please call customer service for assistance: 1-800-766-7000.


Specifications

Specifications

S100A1
4C4.9
ELISA
Purified
S100A1
S100 protein purified from bovine brain was used as the immunogen for the S100 4C4.9 antibody.
11 kDa
0.1 ml
Astrocyte Markers, Breast Cancer, Cancer, Cell Biology, Cellular Markers, Cytoskeleton Markers, Hypoxia, Lipid and Metabolism, Neuronal Cell Markers, Neuroscience, Peroxisome Markers, Signal Transduction
Primary
6271
Human, Mouse, Rat, Bovine
ELISA
DyLight 680
50mM Sodium Borate with 0.05% Sodium Azide
protein S100-A1, S100 alpha, S100 calcium binding protein A1, S100 calcium-binding protein A1S100, S-100 protein alpha chain, S-100 protein subunit alpha, S100 protein, alpha polypeptide, S100A, S100-alpha
Mouse
IgG2a Kappa
Protein A purified
RUO
Store at 4C in the dark.
Monoclonal
S100 belongs to the family of calcium binding proteins. S100A and S100B proteins are two members of the S100 family. S100A is composed of an alpha and beta chain whereas S100B is composed of two beta chains. S-100 protein has been found in normal melanocytes, Langerhans cells, histiocytes, chondrocytes, lipocytes, skeletal and cardiac muscle, Schwann cells, epithelial and myoepithelial cells of the breast, salivary and sweat glands, as well as in glial cells. Neoplasms derived from these cells also express S-100 protein, albeit non-uniformly. A large number of well-differentiated tumors of the salivary gland, adipose and cartilaginous tissue, and Schwann cell-derived tumors express S-100 protein. Almost all malignant melanomas and cases of histiocytosis X are positive for S-100 protein. Despite the fact that S-100 protein is an ubiquitous substance, its demonstration is of great value in the identification of several neoplasms, particularly melanomas and their metastases.
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