NEC1 rabbit pAb

NEC1 rabbit pAb

AO-06-ES14532-100

NEC1 rabbit pAb 100μL

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Antibody Product Overview

ELK.NoES14532
Product nameNEC1 rabbit pAb
ReactivityHuman; Mouse;Rat
ApplicationsWB
Other name
Size100μL
Unit price ($)248
Human gene ID5122
Human Swiss-ProtP29120
SourceRabbit
IsotypeIgG
TargetNEC1
Fields
Gene namePCSK1 NEC1
Protein nameNEC1
Human gene linkView Human Gene
Human Swiss linkView Human Swiss-Prot
Mouse gene ID18548
Mouse gene linkView Mouse Gene
Mouse Swiss-ProtP63239
Mouse Swiss linkView Mouse Swiss-Prot
Rat gene ID100911216
Rat gene linkView Rat Gene
Rat Swiss-ProtP28840
Rat Swiss linkView Rat Swiss-Prot
ImmunogenSynthesized peptide derived from human NEC1 AA range: 125-175
SpecificityThis antibody detects endogenous levels of NEC1 at Human/Mouse/Rat
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
ClonalityPolyclonal
DilutionWB 1:500-2000
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)83kD
Observed band (KD)
BackgroundThis gene encodes a member of the subtilisin-like proprotein convertase family, which includes proteases that process protein and peptide precursors trafficking through regulated or constitutive branches of the secretory pathway. The encoded protein undergoes an initial autocatalytic processing event in the ER to generate a heterodimer which exits the ER and sorts to subcellular compartments where a second autocatalytic even takes place and the catalytic activity is acquired. The protease is packaged into and activated in dense core secretory granules and expressed in the neuroendocrine system and brain. This gene encodes one of the seven basic amino acid-specific members which cleave their substrates at single or paired basic residues. It functions in the proteolytic activation of polypeptide hormones and neuropeptides precursors. Mutations in this gene have been associated with susceptibility to obesity and proprotein convertase 1/3 deficiency. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene [provided by RefSeq, Jan 2014],
Functioncatalytic activity:Release of protein hormones, neuropeptides and renin from their precursors, generally by hydrolysis of -Lys-Arg-|- bonds.,cofactor:Calcium.,disease:Defects in PCSK1 are the cause of proprotein convertase 1 deficiency (PC1 deficiency) [MIM:600955]. PC1 deficiency is characterized by obesity, hypogonadism, hypoadrenalism, reactive hypoglycemia as well as marked small-intestinal absorptive dysfunction It is due to impaired processing of prohormones.,function:Involved in the processing of hormone and other protein precursors at sites comprised of pairs of basic amino acid residues. Substrates include POMC, renin, enkephalin, dynorphin, somatostatin and insulin.,polymorphism:Genetic variations in PCSK1 define the body mass index quantitative trait locus 12 (BMIQ12) [MIM:612362]. Variance in body mass index is a susceptibility factor for obesity.,similarity:Belongs to the pe
Subcellular locationCytoplasmic vesicle, secretory vesicle. Localized in the secretion granules.
Expression

Additional Images

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Western blot analysis of lysates from 293T cells, primary antibody was diluted at 1:1000, 4°over night
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: AO-06-ES14532-100
: 10 Produits
Hurry! only 10 items left in stock.

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