SC23A rabbit pAb

SC23A rabbit pAb

AO-06-ES13191-100

SC23A rabbit pAb 100μL

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Antibody Product Overview

ELK.NoES13191
Product nameSC23A rabbit pAb
ReactivityHuman; Mouse
ApplicationsWB
Other nameProtein transport protein Sec23A (SEC23-related protein A)
Size100μL
Unit price ($)248
Human gene ID10484
Human Swiss-ProtQ15436
SourceRabbit
IsotypeIgG
TargetSC23A
Fields>>Protein processing in endoplasmic reticulum
Gene nameSEC23A
Protein nameSC23A
Human gene linkView Human Gene
Human Swiss linkView Human Swiss-Prot
Mouse gene ID20334
Mouse gene linkView Mouse Gene
Mouse Swiss-ProtQ01405
Mouse Swiss linkView Mouse Swiss-Prot
Rat gene ID
Rat gene link
Rat Swiss-Prot
Rat Swiss link
ImmunogenSynthesized peptide derived from human SC23A AA range: 352-402
SpecificityThis antibody detects endogenous levels of SC23A at Human/Mouse
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.308% 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)
Observed band (KD)85kD
BackgroundThe protein encoded by this gene is a member of the SEC23 subfamily of the SEC23/SEC24 family. It is part of a protein complex and found in the ribosome-free transitional face of the endoplasmic reticulum (ER) and associated vesicles. This protein has similarity to yeast Sec23p component of COPII. COPII is the coat protein complex responsible for vesicle budding from the ER. The encoded protein is suggested to play a role in the ER-Golgi protein trafficking. [provided by RefSeq, Jul 2008],
Functiondisease:Defects in SEC23A are the cause of craniolenticulosutural dysplasia (CLSD) [MIM:607812]. Cranio-lenticulo-sutural dysplasia (CLSD) is an autosomal recessive syndrome characterized by late-closing fontanels, sutural cataracts, facial dysmorphisms and skeletal defects.,function:Component of the COPII coat, that covers ER-derived vesicles involved in transport from the endoplasmic reticulum to the Golgi apparatus. COPII acts in the cytoplasm to promote the transport of secretory, plasma membrane, and vacuolar proteins from the endoplasmic reticulum to the Golgi complex.,similarity:Belongs to the SEC23/SEC24 family. SEC23 subfamily.,subcellular location:In the ribosome-free transitional face of the ER and associated vesicles.,subunit:COPII is composed of at least five proteins: the Sec23/24 complex, the Sec13/31 complex and Sar1. Interacts with SEC23IP. Interacts with HTR4 (By simila
Subcellular locationCytoplasmic vesicle, COPII-coated vesicle membrane ; Peripheral membrane protein ; Cytoplasmic side . Endoplasmic reticulum membrane ; Peripheral membrane protein ; Cytoplasmic side . Cytoplasm, cytosol . Enriched at endoplasmic reticulum exit sites, also known as transitional endoplasmic reticulum (tER). .
ExpressionUbiquitously expressed.

Additional Images

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Western blot analysis of lysates from K562 cells, primary antibody was diluted at 1:1000, 4°over night
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: AO-06-ES13191-100
: 10 Items
Hurry! only 10 items left in stock.

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