S100B Polyclonal Antibody, Invitrogen™
Manufacturer: Fischer Scientific
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | FEPA5145376-Each-of-1 | In Stock | ₹ 15,913.20 |
FEPA5145376 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 15,913.20
GST (18%): ₹ 2,864.376
Total Price: ₹ 18,777.576
Antigen
S100B
Classification
Polyclonal
Conjugate
Unconjugated
Gene
S100B
Gene Alias
AI850290, Bpb, hypothetical protein LOC525716, NEF, protein S100-B, S100, S100 calcium binding protein B, S100 calcium binding protein beta (neural), S100 calcium-binding protein B, S100 calcium-binding protein beta (neural), S-100 calcium-binding protein beta subunit, S100 calcium-binding protein, beta (neural), S-100 calcium-binding protein, beta chain, S100 protein beta chain, S-100 protein beta chain, S-100 protein subunit beta, S100 protein, beta polypeptide, S100 protein, beta polypeptide, neural, S100B, S100-B, S100beta, S100P
Host Species
Rabbit
Purification Method
Protein A
Regulatory Status
RUO
Gene ID (Entrez)
100623510, 20203, 25742, 6285
Content And Storage
Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Isotype
IgG
Applications
Immunocytochemistry, Immunohistochemistry (Paraffin), Western Blot
Concentration
0.5 mg/mL
Formulation
PBS with 50% glycerol and 0.05% Proclin 300, pH 7.4
Gene Accession No.
P04271, P04631, P50114
Gene Symbols
S100B
Immunogen
Recombinant Human S100B protein, Met1-Glu92 (Accession #P04271)
Quantity
20 μL
Primary or Secondary
Primary
Target Species
Human, Mouse, Porcine, Rat
Form
Liquid
Related Products
Description
- S100B is a member of the S100 family of proteins containing 2 EF-hand calcium-binding motifs
- S100 proteins are localized in the cytoplasm and/or nucleus of a wide range of cells and are involved in the regulation of a number of cellular processes such as cell cycle progression and differentiation
- S100B may function in neurite extension, proliferation of melanoma cells, stimulation of Ca2+ fluxes, inhibition of PKC-mediated phosphorylation, astrocytosis and axonal proliferation, and inhibition of microtubule assembly
- Chromosomal rearrangements and altered expression of this gene have been implicated in several diseases, including Alzheimer's disease, Down's syndrome, epilepsy, amyotrophic lateral sclerosis, melanoma, and type I diabetes.