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anti-SLC2A1 antibody product blog

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Posted on 2017-06-11 15:32:21 by mybiosource_staff
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Tags: Antibody; Monoclonal Antibody; anti-SLC2A1 antibody; SLC2A1;
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The SLC2A1 slc2a1 (Catalog #MBS9131361) is an Antibody produced from Rabbit and is intended for research purposes only. The product is available for immediate purchase. The SLC2A1 Monoclonal Antibody reacts with Human, Mouse, Rat and may cross-react with other species as described in the data sheet. MyBioSource\'s SLC2A1 can be used in a range of immunoassay formats including, but not limited to, Western Blot (WB), Immunohistochemistry (IHC), Immunofluorescence (IF).
WB: 1:500 - 1:2000
IHC: 1:50 - 1:200
IF: 1:50 - 1:200. Researchers should empirically determine the suitability of the SLC2A1 slc2a1 for an application not listed in the data sheet. Researchers commonly develop new applications and it is an integral, important part of the investigative research process.

The SLC2A1 slc2a1 product has the following accession number(s) (GI #115502394) (NCBI Accession #P11166.2) (Uniprot Accession #P11166). Researchers may be interested in using Bioinformatics databases such as those available at The National Center for Biotechnology Information (NCBI) website for more information about accession numbers and the proteins they represent. Even researchers unfamiliar with bioinformatics databases will find the NCBI databases to be quite user friendly and useful.

To buy or view more detailed product information and pricing, please click on the technical datasheet page below:


Please refer to the product datasheet for known applications of a given antibody. We\'ve tested the SLC2A1 Monoclonal Antibody with the following immunoassay(s):
Western Blot (WB) (Western blot analysis of extracts of various cell lines, using SLC2A1 antibody.
Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) (MBS128200) at 1:10000 dilution.
Lysates/proteins: 25ug per lane.
Blocking buffer: 3% nonfat dry milk in TBST.)
Western Blot (WB) SLC2A1.

Immunohistochemistry (IHC) (Immunohistochemistry of paraffin-embedded mouse kidney using SLC2A1 antibody at dilution of 1:100 (40x lens).)
Immunohistochemistry (IHC) SLC2A1.

Immunohistochemistry (IHC) (Immunohistochemistry of paraffin-embedded human mammary cancer using SLC2A1 antibody at dilution of 1:100 (40x lens).)
Immunohistochemistry (IHC) SLC2A1.

Immunohistochemistry (IHC) (Immunohistochemistry of paraffin-embedded human liver using SLC2A1 antibody at dilution of 1:100 (40x lens).)
Immunohistochemistry (IHC) SLC2A1.

Immunohistochemistry (IHC) (Immunohistochemistry of paraffin-embedded human kidney using SLC2A1 antibody at dilution of 1:100 (40x lens).)
Immunohistochemistry (IHC) SLC2A1.

Immunohistochemistry (IHC) (Immunohistochemistry of paraffin-embedded mouse liver using SLC2A1 antibody at dilution of 1:100 (40x lens).)
Immunohistochemistry (IHC) SLC2A1.

Immunofluorescence (IF) (Immunofluorescence analysis of HepG2 cells using SLC2A1 antibody.)
Immunofluorescence (IF) SLC2A1.

Immunofluorescence (IF) (Immunofluorescence analysis of MCF-7 cells using SLC2A1 antibody.)
Immunofluorescence (IF) SLC2A1.

Immunofluorescence (IF) (Immunofluorescence analysis of HeLa cells using SLC2A1 antibody.)
Immunofluorescence (IF) SLC2A1.

This gene encodes a major glucose transporter in the mammalian blood-brain barrier. The encoded protein is found primarily in the cell membrane and on the cell surface, where it can also function as a receptor for human T-cell leukemia virus (HTLV) I and II. Mutations in this gene have been found in a family with paroxysmal exertion-induced dyskinesia.

Immunogen: Recombinant protein of human SLC2A1. Storage Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3. In general, we may offer more than one antibody to a given target to enable options for the researcher. Available antibodies recognizing SLC2A1 are readily searchable from our website. Different antibodies against the same target such as SLC2A1 may be optimized or tested for different applications and species. This enables researchers to select the option that may be best for their model system, to screen more than antibody to determine which one may be best for their model system, as well as to use more than one antibody to follow up on and validate their results.
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