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Apolipoprotein B (Apo B), Polyclonal Antibody

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產(chǎn)品名稱: Apolipoprotein B (Apo B), Polyclonal Antibody
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Apolipoprotein B (Apo B), Polyclonal Antibody


Apolipoprotein B (Apo B), Polyclonal Antibody  的詳細(xì)介紹
Product Name

Apolipoprotein B (Apo B) (APOB), Polyclonal Antibody

Full Product Name

Goat anti Apo B

Product Synonym Names
Goat Antibody to Human Apolipoprotein B (Apo B)
Product Gene Name

anti-APOB antibody

[Similar Products]
Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
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Chromosome Location
Chromosome: 2; NC_000002.11 (21224301..21266945, complement). Location: 2p24-p23
OMIM
107730
3D Structure
ModBase 3D Structure for P04114
Clonality
Polyclonal
Host
Goat
Species Reactivity
Human
Specificity
Apolipoprotein B (Apo B) (Monospecific by IEP with neat antibody versus 2X pooled human serum and neat pooled human plasma.)
Purity/Purification
Defribrinated, delipidized and adsorbed by solid phase chromatography. Product is 0.2um filtered.
Form/Format
Monospecific, Liquid
Concentration
Total protein: 8.0 g/dL (lot specific)
Preservative
0.1% Sodium Azide
Immunogen
Purified Human Apolipoprotein B
Titer
26mg/ml (Becker)
Buffer
0.05M Tris-HC1, pH 7.5 containing 0.5 M Sodium Chloride
Preparation and Storage
Short term (up to 7 days) store at 2-8 degree C. Long term, aliquot and store at -20 degree C. If aliquoted for long term storage, fill volume should be equal to or greater than 50% of the nominal fill volume of the vial used. Avoid repeated freeze/thaw cycles.
ISO Certification
Manufactured in an ISO 13485:2003 and EN ISO 13485:2012 Certified Laboratory.
Other Notes
Small volumes of anti-APOB antibody vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.
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Product Categories/Family for anti-APOB antibody
Polyclonal Antibodies to Lipoproteins
NCBI/Uniprot data below describe general gene information for APOB. It may not necessarily be applicable to this product.
NCBI GI #
105990532
NCBI GeneID
338
NCBI Accession #
NP_000375.2 [Other Products]
NCBI GenBank Nucleotide #
NM_000384.2 [Other Products]
UniProt Primary Accession #
P04114 [Other Products]
UniProt Secondary Accession #
O00502; P78479; P78480; P78481; Q13779; Q13785; Q13786; Q13787; Q13788; Q4ZG63; Q53QC8[Other Products]
UniProt Related Accession #
P04114[Other Products]
Molecular Weight
515,605 Da[Similar Products]
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NCBI Official Full Name
apolipoprotein B-100
NCBI Official Synonym Full Names
apolipoprotein B (including Ag(x) antigen)
NCBI Official Symbol
APOB??[Similar Products]
NCBI Official Synonym Symbols
FLDB; LDLCQ4
??[Similar Products]
NCBI Protein Information
apolipoprotein B-100; apoB-48; apoB-100; apo B-100; mutant Apo B 100; apolipoprotein B48
UniProt Protein Name
Apolipoprotein B-100
Protein Family
Apolipoprotein
UniProt Gene Name
APOB??[Similar Products]
UniProt Synonym Gene Names
Apo B-100; Apo B-48??[Similar Products]
UniProt Entry Name
APOB_HUMAN
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NCBI Summary for APOB
This gene product is the main apolipoprotein of chylomicrons and low density lipoproteins. It occurs in plasma as two main isoforms, apoB-48 and apoB-100: the former is synthesized exclusively in the gut and the latter in the liver. The intestinal and the hepatic forms of apoB are encoded by a single gene from a single, very long mRNA. The two isoforms share a common N-terminal sequence. The shorter apoB-48 protein is produced after RNA editing of the apoB-100 transcript at residue 2180 (CAA->UAA), resulting in the creation of a stop codon, and early translation termination. Mutations in this gene or its regulatory region cause hypobetalipoproteinemia, normotriglyceridemic hypobetalipoproteinemia, and hypercholesterolemia due to ligand-defective apoB, diseases affecting plasma cholesterol and apoB levels. [provided by RefSeq, Jul 2008]
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UniProt Comments for APOB
Function: Apolipoprotein B is a major protein constituent of chylomicrons (apo B-48), LDL (apo B-100) and VLDL (apo B-100). Apo B-100 functions as a recognition signal for the cellular binding and internalization of LDL particles by the apoB/E receptor.

Subcellular location: Secreted.

Induction: Up-regulated in response to enterovirus 71 (EV71) infection (at protein level). Ref.34

Post-translational modification: Palmitoylated; structural requirement for proper assembly of the hydrophobic core of the lipoprotein particle. Ref.31

Involvement in disease: Defects in APOB are a cause of familial hypobetalipoproteinemia type 1 (FHBL1) [

MIM:107730]. A disorder characterized by highly reduced plasma concentrations of low density lipoproteins, and dietary fat malabsorption. Clinical presentation may vary from no symptoms to severe gastrointestinal and neurological dysfunction similar to abetalipoproteinemia. Ref.46Defects in APOB are a cause of familial ligand-defective apolipoprotein B-100 (FDB) [

MIM:144010]. FDB is a dominantly inherited disorder of lipoprotein metabolism leading to hypercholesterolemia and increased proneness to coronary artery disease (CAD). The plasma cholesterol levels are dramatically elevated due to impaired clearance of LDL particles by defective APOB/E receptors. Ref.40 Ref.42 Ref.44 Ref.49Note=Defects in APOB associated with defects in other genes (polygenic) can contribute to hypocholesterolemia.

Sequence similarities: Contains 1 vitellogenin domain.

RNA editing: Edited at position 2180.The stop codon (UAA) at position 2180 is created by RNA editing. Apo B-48, derived from the fully edited RNA, is produced only in the intestine and is found in chylomicrons. Apo B-48 is a shortened form of apo B-100 which lacks the LDL-receptor region. The unedited version (apo B-100) is produced by the liver and is found in the VLDL and LDL.

Sequence caution: The sequence AAA51752.1 differs from that shown. Reason: Frameshift at positions 942, 951, 1139, 1165, 1164, 1371 and 1385.
Research Articles on APOB
1. The low plasma Apo-B100 and Apo-AI concentrations in the patients with Anderson disease were mainly related to low rates of production.
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Precautions
All of MyBioSource's Products are for scientific laboratory research purposes and are not for diagnostic, therapeutics, prophylactic or in vivo use. Through your purchase, you expressly represent and warrant to MyBioSource that you will properly test and use any Products purchased from MyBioSource in accordance with industry standards. MyBioSource and its authorized distributors reserve the right to refuse to process any order where we reasonably believe that the intended use will fall outside of our acceptable guidelines.
Disclaimer
While every efforts were made to ensure the accuracy of the information provided in this datasheet, MyBioSource will not be liable for any omissions or errors contained herein. MyBioSource reserves the right to make changes to this datasheet at any time without prior notice.

It is the responsibility of the customer to report product performance issues to MyBioSource within 30 days of receipt of the product. Please visit our Terms & Conditions page for more information.
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