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MABT837

Sigma-Aldrich

Anti-LBPA Antibody, clone 6C4

clone 6C4, from mouse

Sinônimo(s):

LBPA

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About This Item

Código UNSPSC:
12352203
eCl@ss:
32160702
NACRES:
NA.41

fonte biológica

mouse

Nível de qualidade

forma do anticorpo

purified immunoglobulin

tipo de produto de anticorpo

primary antibodies

clone

6C4, monoclonal

reatividade da espécie (prevista por homologia)

all

técnica(s)

ELISA: suitable
dot blot: suitable
electron microscopy: suitable
immunocytochemistry: suitable

Isotipo

IgG1κ

Condições de expedição

wet ice

modificação pós-traducional do alvo

unmodified

Informações sobre genes

bacterial ... Lbpa(61281717)

Descrição geral

Lyso bis-phosphatidic acid (LBPA, Lysobisphosphatidic acid, L(bis)PA) is a lipid that is exclusively located in late endosomes and is used as a late endosome marker. One of the characteristic features of late endosomes is a complex system of internal membranes within the lumen that contains large amounts of the unique, poorly degradable LBPA, and thus forms a specialized membrane domain within endosomes. Late endosomes function not only as a major protein-sorting compartment, but also an obligatory station for LDL and other endocytosed ligands destined for degradation. Research shows that the LBPA-rich membranes within late endosomes regulate cholesterol transport, presumably by acting as a collection and distribution device. The genetic disease Niemann–Pick type C (NPC) is characterized by both lysosomal and endosomal storage disorders. In skin fibroblasts from NPC patients, cholesterol accumulation is seen within vesicles containing late endosome markers LBPA and Rab7.

Especificidade

Clone 6C4 specifically detects LBPA, but not PC, PE, SM, PS, CL, PI, Sul, Chol, Cer, or CE purified from baby hamster kidney (BHK) cell lipid extract (Kobayahsi, T., et al. (1998). Nature. 392(6672):193-197).
Target molecule is not species-specific.

Imunogênio

Endosomal membranes from baby hamster kidney fibroblasts (BHK) corresponding to Hamster LBPA.

Aplicação

Immunocytochemistry Analysis: 4.0 µg/mL from a representative lot detected LBPA in A431, HUVEC and NIH/3T3 cells.
Immunocytochemistry Analysis: A representative lot detected late endosome LBPA immunoreactivity by fluorescent immunocytochemistry using MLN64-overexpressing MCF7 cells (Alpy, F., et al. (2001). J Biol Chem. 276(6):4261-4269).
Immunocytochemistry Analysis: A representative lot detected late endosome LBPA immunoreactivity in skin fibroblasts from healthy donors, as well as Niemann–Pick type C (NPC) and Tay-Sachs disease patients by fluorescent immunocytochemistry (Kobayahsi, T., et al. (1999). Nat Cell Biol. 1(2):113-118).
Immunocytochemistry Analysis: A representative lot detected late endosome LBPA immunoreactivity in baby hamster kidney (BHK) cells by fluorescent immunocytochemistry (Kobayahsi, T., et al. (1998). Nature. 392(6672):193-197).
Electron Microscopy Analysis: A representative lot detected similar cellular LBPA distribution in the skin fibroblasts from autosomal recessive Niemann–Pick type C disease (NPC) patients as seen in baby hamster kidney (BHK) cells (Kobayahsi, T., et al. (1999). Nat Cell Biol. 1(2):113-118).
Electron Microscopy Analysis: A representative lot detected LBPA immunoreactivity specifically associated with the late endosomes in baby hamster kidney (BHK) cells, but not the lgp120-positive limiting membranes of the same endosomes (Kobayahsi, T., et al. (1998). Nature. 392(6672):193-197).
ELISA Analysis: A representative lot specifically detected wells coated with total baby hamster kidney (BHK) cell lipid extract or purified LBPA, but not other lipids (PC, PE, SM, PS, CL, or PI) purified BHK lipid extract (Kobayahsi, T., et al. (1998). Nature. 392(6672):193-197)
Dot Blot Analysis: A representative lot specifically detected purified LBPA spotted on a HPTLC plate, but not other lipids (PC, PE, SM, PS, CL, PI, Sul, Chol, Cer, CE) purified from baby hamster kidney (BHK) cell lipid extract (Kobayahsi, T., et al. (1998). Nature. 392(6672):193-197).
Research Category
Cell Structure
Research Sub Category
Adhesion (CAMs)
This Anti-LBPA Antibody, clone 6C4 is validated for use in Immunocytochemistry, Electron Microscopy, ELISA and Dot Blot for the detection of LBPA.

Qualidade

Evaluated by Immunocytochemistry in HeLa cells.

Immunocytochemistry Analysis: 4.0 µg/mL of this antibody stained late endosomes in HeLa cells.

forma física

Format: Purified
Protein G Purified
Purified mouse monoclonal IgG1κ antibody in buffer containing 0.1 M Tris-Glycine (pH 7.4), 150 mM NaCl with 0.05% sodium azide.

Armazenamento e estabilidade

Stable for 1 year at 2-8°C from date of receipt.

Outras notas

Concentration: Please refer to lot specific datasheet.

Exoneração de responsabilidade

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

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Código de classe de armazenamento

12 - Non Combustible Liquids

Classe de risco de água (WGK)

WGK 1

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable


Certificados de análise (COA)

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Late endosomal membranes rich in lysobisphosphatidic acid regulate cholesterol transport.
Kobayashi, T; Beuchat, MH; Lindsay, M; Frias, S; Palmiter, RD; Sakuraba, H; Parton, RG; Gruenberg, J
Nature Cell Biology null
Jessica Venugopal et al.
Scientific reports, 12(1), 16437-16437 (2022-10-01)
Sickle cell disease (SCD) is associated with altered plasma and erythrocyte lipid profiles. In a previous study, SCD mice with deficiency of proprotein convertase subtilisin/kexin type 9 (PCSK9) were observed to have more severe anemia and increased sickling compared to control
A lipid associated with the antiphospholipid syndrome regulates endosome structure and function.
Kobayashi, T; Stang, E; Fang, KS; de Moerloose, P; Parton, RG; Gruenberg, J
Nature null
F Alpy et al.
The Journal of biological chemistry, 276(6), 4261-4269 (2000-10-29)
MLN64 is a transmembrane protein that shares homology with the cholesterol binding domain (START domain) of the steroidogenic acute regulatory protein. The steroidogenic acute regulatory protein is located in the inner membrane of mitochondria, where it facilitates cholesterol import into
Ruochen Zang et al.
Proceedings of the National Academy of Sciences of the United States of America, 117(50), 32105-32113 (2020-11-27)
Cholesterol 25-hydroxylase (CH25H) is an interferon (IFN)-stimulated gene that shows broad antiviral activities against a wide range of enveloped viruses. Here, using an IFN-stimulated gene screen against vesicular stomatitis virus (VSV)-SARS-CoV and VSV-SARS-CoV-2 chimeric viruses, we identified CH25H and its

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