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The protein encoded by SLURP1 is a member of the Ly6/uPAR family but lacks a GPI-anchoring signal sequence. Zusätzlich bieten wir Ihnen SLURP1 Antikörper (37) und SLURP1 Kits (6) und viele weitere Produktgruppen zu diesem Protein an.
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Human SLURP1 Protein expressed in Wheat germ - ABIN1320581
Fujii, Horiguchi, Sunaga, Moriwaki, Misawa, Kasahara, Tsuji, Kawashima: SLURP-1, an endogenous ?7 nicotinic acetylcholine receptor allosteric ligand, is expressed in CD205(+) dendritic cells in human tonsils and potentiates lymphocytic cholinergic activity. in Journal of neuroimmunology 2014
novel splice site mutation c.58+5G>T in mal (zeige MAL Proteine) de Meleda in India
Results of this study suggest understand Mal (zeige MAL Proteine) de Meleda, it will be important to identify proteins that interact with mutatated SLURP1. In any such studies, it will be important to assess binding of mutant SLURP1 proteins that cause Mal (zeige MAL Proteine) de Meleda.
To our knowledge, the present study is the fi rst (zeige SLC22A12 Proteine) report on molecular investigation of Mal (zeige MAL Proteine) de Meleda from Libya.
This supports the hypothesis that the antiproliferative activity of SLURP-1 is related to 'metabotropic' signaling pathway through alpha7-nAChR (zeige CHRNA7 Proteine), that activates intracellular signaling cascades without opening the receptor channel.
SLURP1 participates in pathophysiology of psoriasis by regulating keratinocyte proliferation and differentiation, and by suppressing the growth of S. aureus
Palmoplantar keratoderma of the Gamborg-Nielsen type is caused by mutations in the SLURP1 gene and represents a variant of Mal (zeige MAL Proteine) de Meleda.
rSLURP-1 decreased production of TNFalpha (zeige TNF Proteine) by T-cells, downregulated IL-1 beta (zeige IL1B Proteine) and IL-6 (zeige IL6 Proteine) secretion by macrophages, and moderately upregulated IL-10 (zeige IL10 Proteine) production by both types of immunocytes
This report further expands the spectrum of clinical phenotypes associated with mutations in SLURP1 in the Mediterranean population.
mutations in SLURP1 as a cause for mal (zeige MAL Proteine) de Meleda and suggest an ancient founder effect for p.W15R in the western European population.
Those findings suggested that SLURP-1 and stimulus through alpha7 nicotinic ACh (zeige FGFR3 Proteine) receptors actively controlled asthmatic condition by stimulating ciliary beating and also by suppressing airway inflammation.
SLURP1 nonsense mutation is responsible for the pathogenesis of palmoplantar keratoderma.
These data describe the influence of age, sex, genetic background, and ocular surface health on mouse corneal expression of Slurp1, establish the baseline for human tear SLURP1 expression.
Slurp1 in mice has a role in neuromuscular and metabolic phenotypes in addition to its role in palmoplantar keratoderma
Those findings suggest that diminished expression of SLURP-1 in asthma attenuates its negative regulation of airway inflammation, and that perhaps changes in SLURP-1 expression could serve as a marker of airway damage in asthma.
The protein encoded by this gene is a member of the Ly6/uPAR family but lacks a GPI-anchoring signal sequence. It is thought that this secreted protein contains antitumor activity. Mutations in this gene have been associated with Mal de Meleda, a rare autosomal recessive skin disorder. This gene maps to the same chromosomal region as several members of the Ly6/uPAR family of glycoprotein receptors.
secreted Ly-6/uPAR-related protein 1
, secreted LY6/PLAUR domain containing 1
, ARS component B
, ARS(component B)-81/S
, anti-neoplastic urinary protein
, lymphocyte antigen 6-like secreted
, secreted Ly6/uPAR related protein 1
, Ars component B
, secreted Ly-6/uPAR related protein 1