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LMBRD1, Blocking Peptide

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产品名称: LMBRD1, Blocking Peptide
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简单介绍

LMBRD1, Blocking Peptide


LMBRD1, Blocking Peptide  的详细介绍
Product Name

LMBRD1, Blocking Peptide

Full Product Name

LMBRD1 Peptide

Product Synonym Names
NESI; LMBD1; MAHCF; C6orf209; NESI; BM-021; CD001; MSTP044; Probable lysosomal cobalamin transporter; HDAg-L-interacting protein NESI; LMBR1 domain containing 1
Product Gene Name

LMBRD1 blocking peptide

[Similar Products]
Antibody/Peptide Pairs
LMBRD1 peptide (MBS153047) is used for blocking the activity of LMBRD1 antibody (MBS150185)
Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
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OMIM
phenotype 612625
3D Structure
ModBase 3D Structure for Q9NUN5
Form/Format
Liquid
Concentration
200 ug/mL (lot specific)
Species
Human
Buffer
PBS pH 7.2 (10 mM NaH2PO4, 10 mM Na2HPO4, 130 mM NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide
Location
18 amino acids near the carboxy terminus of human LMBRD1.
Preparation and Storage
Store LMBRD1 peptide at -20 degree C, stable for one year.
Other Notes
Small volumes of LMBRD1 blocking peptide 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 LMBRD1 blocking peptide
Blocking (BL)
Application Notes for LMBRD1 blocking peptide
LMBRD1 peptide is used for blocking the activity of LMBRD1 antibody.
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NCBI/Uniprot data below describe general gene information for LMBRD1. It may not necessarily be applicable to this product.
NCBI GI #
261878497
NCBI GeneID
55788
NCBI Accession #
NP_060838 [Other Products]
NCBI GenBank Nucleotide #
NM_018368.3 [Other Products]
UniProt Primary Accession #
Q9NUN5 [Other Products]
UniProt Secondary Accession #
Q5VUN6; Q86Y70; Q96FW4; Q9BY56; Q9NZD6; A8K204; E1P531[Other Products]
UniProt Related Accession #
Q9NUN5[Other Products]
Molecular Weight
21,394 Da
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NCBI Official Full Name
probable lysosomal cobalamin transporter
NCBI Official Synonym Full Names
LMBR1 domain containing 1
NCBI Official Symbol
LMBRD1  [Similar Products]
NCBI Official Synonym Symbols
NESI; LMBD1; MAHCF; C6orf209
  [Similar Products]
NCBI Protein Information
probable lysosomal cobalamin transporter; HDAg-L-interacting protein NESI; liver regeneration p-53 related protein; nuclear export signal-interacting protein; hepatitis delta antigen-L interacting protein
UniProt Protein Name
Probable lysosomal cobalamin transporter
UniProt Synonym Protein Names
HDAg-L-interacting protein NESI; LMBR1 domain-containing protein 1; Nuclear export signal-interacting protein
UniProt Gene Name
LMBRD1  [Similar Products]
UniProt Synonym Gene Names
C6orf209; NESI  [Similar Products]
UniProt Entry Name
LMBD1_HUMAN
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NCBI Summary for LMBRD1
This gene encodes a lysosomal membrane protein that may be involved in the transport and metabolism of cobalamin. This protein also interacts with the large form of the hepatitis delta antigen and may be required for the nucleocytoplasmic shuttling of the hepatitis delta virus. Mutations in this gene are associated with the vitamin B12 metabolism disorder termed, homocystinuria-megaloblastic anemia complementation type F.[provided by RefSeq, Oct 2009]
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UniProt Comments for LMBRD1
LMBRD1: Probable lysosomal cobalamin transporter. Required to export cobalamin from lysosomes allowing its conversion to cofactors. Isoform 3 may play a role in the assembly of hepatitis delta virus (HDV). Defects in LMBRD1 are the cause of methylmalonic aciduria and homocystinuria type cblF (MMAHCF). A disorder of cobalamin metabolism characterized by decreased levels of the coenzymes adenosylcobalamin (AdoCbl) and methylcobalamin (MeCbl). It is due to accumulation of free cobalamin in lysosomes, thus hindering its conversion to cofactors. Clinical features include developmental delay, stomatitis, glossitis, seizures and methylmalonic aciduria responsive to vitamin B12. Belongs to the LIMR family. LMBRD1 subfamily. 4 isoforms of the human protein are produced by alternative splicing.

Protein type: Membrane protein, integral; Membrane protein, multi-pass

Chromosomal Location of Human Ortholog: 6q13

Cellular Component: membrane; lysosomal membrane; integral to membrane; plasma membrane; clathrin-coated endocytic vesicle

Molecular Function: insulin receptor binding; cobalamin binding

Biological Process: negative regulation of glucose import; negative regulation of protein kinase B signaling cascade; vitamin metabolic process; viral reproduction; cobalamin metabolic process; negative regulation of insulin receptor signaling pathway; water-soluble vitamin metabolic process

Disease: Methylmalonic Aciduria And Homocystinuria, Cblf Type
Research Articles on LMBRD1
1. LMBD1 plays an imperative role in mediating and regulating the endocytosis of the IR.
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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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