CYLD (phospho-Ser418) rabbit pAb

CYLD (phospho-Ser418) rabbit pAb

AO-06-ES17131-50

CYLD (phospho-Ser418) rabbit pAb 50μL

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Antibody Product Overview

ELK.NoES17131
Product nameCYLD (phospho-Ser418) rabbit pAb
ReactivityHuman;Rat;Mouse;
ApplicationsWB
Other nameUbiquitin carboxyl-terminal hydrolase CYLD (EC 3.4.19.12) (Deubiquitinating enzyme CYLD) (Ubiquitin thioesterase CYLD) (Ubiquitin-specific-processing protease CYLD)
Size50μL
Unit price ($)148
Human gene ID1540
Human Swiss-ProtQ9NQC7
SourceRabbit
IsotypeIgG
TargetCYLD
Fields>>NF-kappa B signaling pathway;>>Necroptosis;>>Osteoclast differentiation;>>RIG-I-like receptor signaling pathway;>>C-type lectin receptor signaling pathway
Gene nameCYLD CYLD1 KIAA0849 HSPC057
Protein nameCYLD (Ser418)
Human gene linkView Human Gene
Human Swiss linkView Human Swiss-Prot
Mouse gene ID74256
Mouse gene linkView Mouse Gene
Mouse Swiss-ProtQ80TQ2
Mouse Swiss linkView Mouse Swiss-Prot
Rat gene ID312937
Rat gene linkView Rat Gene
Rat Swiss-ProtQ66H62
Rat Swiss linkView Rat Swiss-Prot
ImmunogenSynthesized phosho peptide around human CYLD (Ser418)
SpecificityThis antibody detects endogenous levels of Human CYLD (phospho-Ser418)
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
ClonalityPolyclonal
DilutionWB 1:1000-2000
PurificationThe antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen.
Concentration1 mg/ml
Storage stability-20°C/1 year
Molecular Weight (Da)
Observed band (KD)105kD
BackgroundThis gene is encodes a cytoplasmic protein with three cytoskeletal-associated protein-glycine-conserved (CAP-GLY) domains that functions as a deubiquitinating enzyme. Mutations in this gene have been associated with cylindromatosis, multiple familial trichoepithelioma, and Brooke-Spiegler syndrome. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008],
Functioncatalytic activity:Ubiquitin C-terminal thioester + H(2)O = ubiquitin + a thiol.,disease:Defects in CYLD are the cause of Brooke-Spiegler syndrome (BRSS) [MIM:605041]. BRSS is an autosomal dominant disorder characterized by the appearance of multiple skin appendage tumors such as cylindroma, trichoepithelioma, and spiradenoma. These tumors are typically located in the head and neck region, appear in early adulthood, and gradually increase in size and number throughout life.,disease:Defects in CYLD are the cause of familial cylindromatosis [MIM:132700]; also known as Ancell-Spiegler cylindromas or turban tumor syndrome or dermal eccrine cylindromatosis. CYLD is an autosomal dominant and highly tumor type-specific disorder. The tumors (known as cylindromas because of their characteristic microscopic architecture) are believed to arise from or recapitulate the appearance of the eccrine or a
Subcellular locationCytoplasm . Cytoplasm, perinuclear region. Cytoplasm, cytoskeleton. Cell membrane; Peripheral membrane protein; Cytoplasmic side. Cytoplasm, cytoskeleton, microtubule organizing center, centrosome . Cytoplasm, cytoskeleton, spindle . Cytoplasm, cytoskeleton, cilium basal body . Detected at the microtubule cytoskeleton during interphase. Detected at the midbody during telophase. During metaphase, it remains localized to the centrosome but is also present along the spindle (PubMed:25134987). .
ExpressionDetected in fetal brain, testis, and skeletal muscle, and at a lower level in adult brain, leukocytes, liver, heart, kidney, spleen, ovary and lung. Isoform 2 is found in all tissues except kidney.

Additional Images

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Western Blot analysis of 1 A431 treated with LPS, 2 A431,using primary antibody at 1:1000 dilution. Secondary antibody(catalog#:RS23920) was diluted at 1:10000
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: AO-06-ES17131-50
: 10 Produits
Hurry! only 10 items left in stock.

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