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Anti-Caveolin-1 (phospho-Y14) Antibody

品牌：Antibodies

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規(guī)格：50μl

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Anti-Caveolin-1 (phospho-Y14) Antibody

商品詳情參考文獻(xiàn) 相關(guān)資料

Overview

Name:	Anti-Caveolin-1 (phospho-Y14) Antibody See all Caveolin-1 primary antibodies
Description:	Rabbit polyclonal antibody to Caveolin-1 (phospho-Y14)
Specificity:	p-Caveolin-1 (Y14) pAb detects endogenous levels of Caveolin-1 protein only when phosphorylated at Tyr14.
Applications:	WB
Reactivity:	Human, Mouse, Rat
Immunogen:	Synthetic phosphopeptide derived from human Caveolin-1 around the phosphorylation site of Tyrosine 14.
Host:	Rabbit
Clonality:	Polyclonal
Conjugate:	Unconjugated
Molecular Weight:	~ 20, 25 kDa
Purity:	The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen and the purity is > 95% (by SDS-PAGE).
Product Form:	1 mg/ml in Phosphate buffered saline (PBS) with 0.05% sodium azide, approx. pH 7.2.

Target

Function:	May act as a scaffolding protein within caveolar membranes. Interacts directly with G-protein alpha subunits and can functionally regulate their activity (By similarity). Involved in the costimulatory signal essential for T-cell receptor (TCR)-mediated T-cell activation. Its binding to DPP4 induces T-cell proliferation and NF-kappa-B activation in a T-cell receptor/CD3-dependent manner. Recruits CTNNB1 to caveolar membranes and may regulate CTNNB1-mediated signaling through the Wnt pathway. Negatively regulates TGFB1-mediated activation of SMAD2/3 by mediating the internalization of TGFBR1 from membrane rafts leading to its subsequent degradation (PubMed:25893292).
Tissue Specificity:	Expressed in muscle and lung, less so in liver, brain and kidney.
Involvement in Disease:	Congenital generalized lipodystrophy 3: An autosomal recessive disorder characterized by a near complete absence of adipose tissue, extreme insulin resistance, hypertriglyceridemia, hepatic steatosis and early onset of diabetes. Pulmonary hypertension, primary, 3: A rare disorder characterized by plexiform lesions of proliferating endothelial cells in pulmonary arterioles. The lesions lead to elevated pulmonary arterial pression, right ventricular failure, and death. The disease can occur from infancy throughout life and it has a mean age at onset of 36 years. Penetrance is reduced. Although familial pulmonary hypertension is rare, cases secondary to known etiologies are more common and include those associated with the appetite-suppressant drugs. Partial lipodystrophy, congenital cataracts, and neurodegeneration syndrome: A form of familial partial lipodystrophy associated with congenital cataracts and neurodegeneration leading to cerebellar and spinal cord dysfunction.
Sequence Similarities:	Belongs to the caveolin family.
Post-Translational Modification:	The initiator methionine for isoform 2 is removed during or just after translation. The new N-terminal amino acid is then N-acetylated.
Cellular Location:	Golgi apparatus membrane. Cell membrane. Membrane > Caveola. Membrane raft. Colocalized with DPP4 in membrane rafts. Potential hairpin-like structure in the membrane. Membrane protein of caveolae.
Database Links:	Entrez Gene: 857?Human Entrez Gene: 12389?Mouse Entrez Gene: 25404?Rat Omim: 601047?Human SwissProt: Q03135?Human SwissProt: P49817?Mouse SwissProt: P41350?Rat Unigene: 74034?Human Unigene: 28278?Mouse Unigene: 470537?Mouse Unigene: 22518?Rat
Synonyms:	BSCL3 Antibody CAV Antibody CAV1 Antibody CAV1_HUMAN Antibody caveolae protein, 22 kD Antibody caveolin 1 alpha isoform Antibody caveolin 1 beta isoform Antibody Caveolin 1 caveolae protein 22kDa Antibody Caveolin-1 Antibody Caveolin1 Antibody cell growth-inhibiting protein 32 Antibody CGL3 Antibody LCCNS Antibody MSTP085 Antibody OTTHUMP00000025031 Antibody PPH3 Antibody VIP 21 Antibody VIP21 Antibody
Information:	Target information shown above is from the UniProt Consortium.