Skip to Content
MilliporeSigma
All Photos(2)

Key Documents

MABS483

Sigma-Aldrich

Anti-PL Scramblase 1 Antibody, clone 4D2

clone 4D2, from mouse

Synonym(s):

Phospholipid scramblase 1, PL scramblase 1, Ca(2+)-dependent phospholipid scramblase 1, Erythrocyte phospholipid scramblase, MmTRA1b, PL Scramblase 1

Sign Into View Organizational & Contract Pricing


About This Item

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

biological source

mouse

Quality Level

antibody form

purified immunoglobulin

antibody product type

primary antibodies

clone

4D2, monoclonal

species reactivity

human

technique(s)

immunocytochemistry: suitable
immunoprecipitation (IP): suitable
western blot: suitable

isotype

IgG1κ

NCBI accession no.

UniProt accession no.

shipped in

wet ice

target post-translational modification

unmodified

Gene Information

human ... PLSCR1(5359)

General description

Phospholipid scramblase 1 (UniProt O15162; also known as Ca(2+)-dependent phospholipid scramblase 1, Erythrocyte phospholipid scramblase, MmTRA1b, PL scramblase 1) is encoded by the PLSCR1 (also known as MMTRA1B) gene (Gene ID 5359) in human. Plasma membrane phospholipids are distributed asymmetrically between the inner and outer leaflets. Such asymmetrical distribution collapses in response to blood coagulation and apoptosis, resulting in phospholipid “scrambling” between the two leaflets of the plasma membrane. Flippases, floppases, and scramblases are three types enzymes known to mediate transbilayer lipid motion. Flippases and floppases function via an ATP-dependent mechanism, while scramblases mediate transbilayer movement in a non-selective and energy-independent manner. Originally identified in 1996 as a 37 kDa erythrocyte type II transmembrane protein that mediates calcium-dependent membrane phospholipids redistribution, PL Scramblase 1 is the protein product encoded by the founding member of the PLSCR family of genes (PLSCR1-5). All PLSCR family members, with the exception of PLSCR2, possess a proline-rich N-terminal region containing PxxP and PPxY domains, a cysteine-rich region, a conserved calcium-binding domain (EF-hand-like), and a putative transmembrane region enriched in hydrophobic amino acids. In addition, PLSCR1 contains a nuclear localization signal (NLS) and a DNA-binding domain that are essential for its nuclear localization and associated nuclear function. In addition to PLSCRs, TMEM16 and XKR family members have also been reported to mediate scramblase activity.

Immunogen

Recombinant protein corresponding to human PL Scramblase 1.

Application

Research Category
Signaling
Research Sub Category
Signaling Neuroscience
This Anti-PL Scramblase 1 Antibody, clone 4D2 is validated for use in Western Blotting, Immunoprecipitation, Immunocytochemistry for the detection of PL Scramblase 1 .
Western Blotting Analysis: 0.5 µg/mL from a representative lot detected PL Scramblase 1 in 10 µg of human erythroleukemia K562 and Jurkat cell lysate.
Immunocytochemistry Analysis: A representative lot detected endogenous PLSCR1 in paraformaldehyde-fixed, saponin-permeabilized HT1080 cells (25 µg mAb/mL) by confocal fluorescence microscopy (Zhou, Q., et al, (2000) 95(8):2593-2599).
Immunocytochemistry Analysis: A representative lot detected endogenous PLSCR1 in formaldehyde-fixed, Triton X-100-permeabilized HT1080 cells (5 µg mAb/mL) by confocal fluorescence microscopy (Wiedmer, T., et al, (2003) Biochemistry. 42(5):1227-1233).
Immunoprecipitation Analysis: A representative lot immunoprecipitated exogenously expressed human PLSCR1 constructs from lysates (25 µg mAb/0.5 mL lysate) of transfected murine SVT2 cells (Wiedmer, T., et al, (2003) Biochemistry. 42(5):1227-1233).
Western Blotting Analysis: A representative lot detected human PLSCR1 in lysates from varous human cell lines (PMID 10753839, 12564925, 15308560, 16091359).

Quality

Evaluated by Western Blotting in HeLa cell lysate.

Western Blotting Analysis: 0.5 µg/mL of this antibody detected PL Scramblase 1 in 10 µg of HeLa cell lysate.

Target description

~35 kDa observed

Physical form

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.

Storage and Stability

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

Other Notes

Concentration: Please refer to lot specific datasheet.

Disclaimer

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.

Not finding the right product?  

Try our Product Selector Tool.

Storage Class

12 - Non Combustible Liquids

wgk_germany

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Protein kinase Cdelta mediates retinoic acid and phorbol myristate acetate-induced phospholipid scramblase 1 gene expression: its role in leukemic cell differentiation.
Zhao, KW; Li, X; Zhao, Q; Huang, Y; Li, D; Peng, ZG; Shen, WZ; Zhao, J; Zhou, Q; Chen et al.
Blood null
Palmitoylation of phospholipid scramblase 1 controls its distribution between nucleus and plasma membrane.
Wiedmer, T; Zhao, J; Nanjundan, M; Sims, PJ
Biochemistry null
Phospholipid scramblase 1 binds to the promoter region of the inositol 1,4,5-triphosphate receptor type 1 gene to enhance its expression.
Zhou, Q; Ben-Efraim, I; Bigcas, JL; Junqueira, D; Wiedmer, T; Sims, PJ
The Journal of Biological Chemistry null
Q Zhou et al.
Blood, 95(8), 2593-2599 (2001-02-07)
Interferons (IFNs) mediate their diverse biologic activities through induction of the expression of multiple genes. Whereas the mode of action of certain of these IFN-regulated genes has been well characterized, most of the molecular and cellular events underlying the constellation

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service