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Cytoskeleton Proteins

Gamma-synuclein (1H10) Antibody

$264.00
SKU: 252664
SNCG (Gamma-synuclein) is a 127-amino acid protein (~14kDa), belongs to the synuclein family, which also includes alpha- and beta- synuclein. Three synucleins are located in the neuronal cytosol and enriched in presynaptic terminals, while SNCG is also expressed in many other non-neuronal tissues. SNCG is abnormally expressed in a high percentage of tumor tissues of diversified cancer types, including liver, esophagus, colon, gastric, lung, prostate, cervical and breast cancer, but rarely expressed in tumor-matched non-neoplastic adjacent tissues.
List price: $0.00
Price: $264.00

Calcyclin (7D11) Antibody

$264.00
SKU: 252639
Calcyclin (S100A6) 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, involved in the regulation of a number of cellular processes such as cell cycle progression and differentiation. This protein may function in stimulation of Ca2+-dependent insulin release, stimulation of prolactin secretion and exocytosis. Chromosomal rearrangements and altered expression of this gene have been implicated in melanoma.
List price: $0.00
Price: $264.00

cTnI (3A10) Antibody

$264.00
SKU: 252637
Troponin I is the inhibitory subunit of troponin, the thin filament regulatory complex which confers calcium-sensitivity to striated muscle actomyosin ATPase activity. Troponin I binds to actin and tropomyosin. Defects in Troponin I are the cause of cardiomyopathies characterized by ventricular anomalies.
List price: $0.00
Price: $264.00

Tau (Ser416) Antibody

$350.00
SKU: 252587
Tau protein promotes microtubule assembly and stability. Tau is also involved in the establishment and maintenance of neural polarity. The C-terminus domain of Tau binds to axonal microtubules whereas the N-terminus domain binds to neural plasma membrane components, therefore suggesting that Tau protein functions as a linker between the two. Axonal polarity is predetermined by tau localization in the domain of the cell body defined by the centrosome. The short isoforms allow plasticity of the cytoskeleton whereas the longer isoforms may preferentially play a role in its stabilization.
List price: $0.00
Price: $350.00

Gap-43 (Ser41) Antibody

$350.00
SKU: 252546
GAP-43 (Growth associated protein-43, neuromodulin) is a cytoplasmic axonal membrane protein that is involved in the neuronal outgrowth and synaptic plasticity of developing and regenerating neurons . Palmitoylated GAP-43 attaches to the membrane via lipid rafts, while the unmodified form is a component of the centrosome. GAP-43 binds to calmodulin in the absence of Ca++ and functions as a substrate for PKC in the nerve growth factor (NGF) signaling pathway.
List price: $0.00
Price: $350.00

SMA Antibody

$245.00
SKU: 252037

Smooth muscle actin (SMA, ACTA2), the human aortic smooth muscle actin gene, is one of six different actin isoforms which have been identified. Actins are highly conserved proteins that are involved in cell motility, structure, and integrity. Alpha-actins are a major constituent of the contractile apparatus. Defects in SMA are the cause of aortic aneurysm familial thoracic type 6, characterized by permanent dilation of the thoracic aorta.

List price: $0.00
Price: $245.00

Annexin I Antibody

$280.00
SKU: 252065
Annexin I is a calcium/phospholipid-binding protein which promotes membrane fusion and is involved in exocytosis. Annexin I regulates phospholipase A2 activity. Annexin I binds from two to four calcium ions with high affinity. Annexin I is phosphorylated by protein kinase C, epidermal growth factor receptor/kinase and TRPM7. Phosphorylation results in loss of the inhibitory activity.
List price: $0.00
Price: $280.00

Ankyrin-1 Antibody

$245.00
SKU: 252063
Ankyrin-1 attaches (ANK1) integral membrane proteins to cytoskeletal elements. Erythrocyte ankyrins link spectrin (beta chain) to the cytoplasmic domain of the erythrocytes anion exchange protein. Defects in ANK1 are a cause of spherocytosis type 1 (SPH1), also called hereditary spherocytosis type 1 (HS1). Spherocytosis is a hematologic disorder leading to chronic hemolytic anemia and characterized by numerous abnormally shaped erythrocytes which are generally spheroidal. Inheritance can be autosomal dominant or recessive.
List price: $0.00
Price: $245.00

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