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Very Low Density Lipoprotein Receptor, Polyclonal Antibody

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產(chǎn)品名稱: Very Low Density Lipoprotein Receptor, Polyclonal Antibody
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Very Low Density Lipoprotein Receptor, Polyclonal Antibody


Very Low Density Lipoprotein Receptor, Polyclonal Antibody  的詳細介紹
Product Name

Very Low Density Lipoprotein Receptor (VLDLR), Polyclonal Antibody

Full Product Name

Polyclonal Antibody to Very Low Density Lipoprotein Receptor (VLDLR)

Product Gene Name

anti-VLDLR antibody

[Similar Products]
Matching Pairs
Unconjugated Antibody: Very Low Density Lipoprotein Receptor (MBS2028288)
Immunogen: Very Low Density Lipoprotein Receptor (MBS2030231)
Matching Pairs
Unconjugated Antibody: Very Low Density Lipoprotein Receptor (MBS2028288)
APC-CY7 Conjugated Antibody: Very Low Density Lipoprotein Receptor (VLDLR) (MBS2050418)
Matching Pairs
Unconjugated Antibody: Very Low Density Lipoprotein Receptor (MBS2028288)
PE Conjugated Antibody: Very Low Density Lipoprotein Receptor (VLDLR) (MBS2050419)
Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
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Immunogen Sequence
Antigen: The target protein is fused with two N-terminal Tags, His-tag and T7-tag and its sequence is listed below.
MGSSHHHHHH SSGLVPRGSH MASMTGGQQM GRGSEF- KCE CSRGYQMDLA TGVCKAVGKE PSLIFTNRRD IRKIGLERKE YIQLVEQLRN TVALDADIAA QKLFWADLSQ KAIFSASIDD KVGRHVKMID NVYNPAAIAV DWVYKTIYWT DAASKTISVA TLDGTKRKFL FNSDLREPAS IAVDPLSGFV YWSDWGEPAK IEKAGMNGFD RRPLVTADIQ WPNGITLDLI KSRLYWLDSK LHMLSSVDLN GQDRRIVLKS LEFLAHPLAL TIFEDRVYWI DGENEAVYGA NKFTGSELAT LVNNLNDAQD IIVYHELVQP SGKNWCEEDM ENGGCEYLCL PA
OMIM
L20470 mRNA
3D Structure
ModBase 3D Structure for P98155
Clonality
Polyclonal
Isotype
IgG
Host
Rabbit
Species Reactivity
Human
Specificity
The antibody is a rabbit polyclonal antibody raised against VLDLR. It has beenselected for its ability to recognize VLDLR in immunohistochemical staining andwestern blotting.
Purity/Purification
Affinity Chromatography
Form/Format
Liquid
Concentration
200ug/ml (lot specific)
Fragment
VLDLR (Lys418~Ala722)
Organism Species
Homo sapiens (Human)
Conjugate
No Conjugate
Immunogen
Recombinant VLDLR (Lys418~Ala722) expressed in E Coli.
Conjugated Antibody
The APC conjugated antibody version of this item is also available as catalog #MBS2050420
Preparation and Storage
Store at 4 degree C for frequent use. Stored at -20 degree C to -80 degree C in a manual defrost freezer for one year without detectable loss of activity. Avoid repeated freeze-thaw cycles.
ISO Certification
Manufactured in an ISO 9001:2008 and ISO 13485:2003 Certified Laboratory.
Supply Chain Verification
Manufactured in a lab with traceable raw materials. Bulk orders can typically be prepared to the customera??s specifications, please inquire.
Other Notes
Small volumes of anti-VLDLR 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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Applications Tested/Suitable for anti-VLDLR antibody
Western Blot (WB), Immunocytochemistry (ICC), Immunohistochemistry (IHC) Formalin/Paraffin, ELISA (EIA)
Application Notes for anti-VLDLR antibody
Western blotting: 1-5ug/mL
Immunocytochemistry in formalin fixed cells: 5-20ug/mL
Immunohistochemistry in formalin fixed frozen section: 5-20ug/mL
Immunohistochemistry in paraffin section: 5-20ug/mL
Enzyme-linked Immunosorbent Assay: 0.05-2ug/mL
Optimal working dilutions must be determined by end user.

Western Blot (WB) of anti-VLDLR antibody
Western Blot: Sample: Recombinant VLDLR, Human.
anti-VLDLR antibody Western Blot (WB) (WB) image
Immunohistochemistry (IHC) of anti-VLDLR antibody
DAB staining on IHC-P; Samples: Human Kidney Tissue.
anti-VLDLR antibody Immunohistochemistry (IHC) (IHC) image
Immunohistochemistry (IHC) of anti-VLDLR antibody
DAB staining on IHC-P; Samples: Human Stomach Tissue.
anti-VLDLR antibody Immunohistochemistry (IHC) (IHC) image
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NCBI/Uniprot data below describe general gene information for VLDLR. It may not necessarily be applicable to this product.
NCBI GI #
65301164
NCBI GeneID
7436
NCBI Accession #
NP_001018066.1 [Other Products]
NCBI GenBank Nucleotide #
NM_001018056.2 [Other Products]
UniProt Primary Accession #
P98155 [Other Products]
UniProt Secondary Accession #
Q5VVF6; B2RMZ7; D3DRH6[Other Products]
UniProt Related Accession #
P98155[Other Products]
Molecular Weight
93,383 Da
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NCBI Official Full Name
very low-density lipoprotein receptor isoform b
NCBI Official Synonym Full Names
very low density lipoprotein receptor
NCBI Official Symbol
VLDLR??[Similar Products]
NCBI Official Synonym Symbols
CAMRQ1; CARMQ1; CHRMQ1; VLDL-R; VLDLRCH
??[Similar Products]
NCBI Protein Information
very low-density lipoprotein receptor
UniProt Protein Name
Very low-density lipoprotein receptor
Protein Family
Very low-density lipoprotein receptor
UniProt Gene Name
VLDLR??[Similar Products]
UniProt Synonym Gene Names
VLDL receptor; VLDL-R??[Similar Products]
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NCBI Summary for VLDLR
The low density lipoprotein receptor (LDLR) gene family consists of cell surface proteins involved in receptor-mediated endocytosis of specific ligands. This gene encodes a lipoprotein receptor that is a member of the LDLR family and plays important roles in VLDL-triglyceride metabolism and the reelin signaling pathway. Mutations in this gene cause VLDLR-associated cerebellar hypoplasia. Alternative splicing generates multiple transcript variants encoding distinct isoforms for this gene. [provided by RefSeq, Aug 2009]
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UniProt Comments for VLDLR
VLDLR: Binds VLDL and transports it into cells by endocytosis. In order to be internalized, the receptor-ligand complexes must first cluster into clathrin-coated pits. Binding to Reelin induces tyrosine phosphorylation of Dab1 and modulation of Tau phosphorylation. Defects in VLDLR are the cause of cerebellar ataxia mental retardation and dysequilibrium syndrome type 1 (CMARQ1); also known as dysequilibrium syndrome (DES) or non- progressive cerebellar disorder with mental retardation. CMARQ1 is a congenital, non-progressive cerebellar ataxia associated with disturbed equilibrium, delayed ambulation, mental retardation and cerebellar hypoplasia. Additional features include short stature, strabismus, pes planus and, rarely, seizures. 2 isoforms of the human protein are produced by alternative splicing.

Protein type: Membrane protein, integral; Receptor, misc.

Chromosomal Location of Human Ortholog: 9p24.2

Cellular Component: clathrin-coated pit; integral component of membrane; lysosomal membrane; membrane; plasma membrane; receptor complex

Molecular Function: apolipoprotein binding; calcium ion binding; calcium-dependent protein binding; low-density lipoprotein receptor activity; protein binding; very-low-density lipoprotein binding; very-low-density lipoprotein receptor activity

Biological Process: axon guidance; cholesterol metabolic process; dendrite morphogenesis; lipid transport; low-density lipoprotein particle receptor catabolic process; memory; negative regulation of transcription from RNA polymerase II promoter; nervous system development; positive regulation of protein kinase activity; receptor-mediated endocytosis; signal transduction; ventral spinal cord development

Disease: Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 1
Research Articles on VLDLR
1. C (p.Cys52Arg) in the VLDLR gene">In the second family, we identified a previously unreported homozygous missense change, c.154T > C (p.Cys52Arg) in the VLDLR gene
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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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