SLC22A18AS Antibodies

AND SLC22A18AS ELISA kits, SLC22A18AS Proteins

Many biological assays use antibodies to detect SLC22A18AS, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with SLC22A18AS in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop SLC22A18AS antibodies...

We validate the specificity of these antibodies to SLC22A18AS by testing them on tissues known to express SLC22A18AS positively and negatively. Browse below to find the SLC22A18AS antibody that suites your experiment. We have 1 of these antibodies and many publications and validation images.

If you cannot find antibodies that fit your needs, contact us for making custom antibodies. We have a full suite of custom antibody services covering from research to diagnostic and therapeutic applications.

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SLC22A18AS Infographic by Boster Bio

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SLC22A18AS (NM_007105) Human Over-expression Lysate

Human

$628
Cat # LS005003
20 µg, 100 µg

SLC22A18AS Overview

Facts about Beckwith-Wiedemann syndrome chromosomal region 1 candidate gene B protein.

SLC22A18AS 3D structure. Source: alphafold

Beckwith-Wiedemann syndrome chromosomal region 1 candidate gene B protein (SLC22A18AS)

Gene Information

Human
Gene Name:	SLC22A18AS
Uniprot:	Q8N1D0
Entrez:	5003

Family

Belongs to:

No superfamily

Alternative Names

BWR1BSolute carrier family 22 member 18 antisense protein; BWSCR1BBeckwith-Wiedemann region 1B; ORCTL2Sbeckwith-Wiedemann syndrome chromosomal region 1 candidate gene B protein; organic cation transporter-like 2 antisense; Organic cation transporter-like protein 2 antisense protein; p27-BWR1Bp27-Beckwith-Wiedemann region 1 B; SLC22A1LSBeckwith-Wiedemann syndrome chromosome region 1, candidate b; solute carrier family 22 (organic cation transporter), member 18 antisense; solute carrier family 22 (organic cation transporter), member 1-like antisense; Solute carrier family 22 member 1-like antise

Molecular Weight

Mass (kDA):
27.061 kDA

Genomic Context


Human

Location:	11p15.4
Sequence:	11; NC_000011.10 (2887344..2905504, complement)

Diseases

Adenocarcinoma
Cell Transformation, Neoplastic
Lung Neoplasms
Malignant Neoplasm Of Breast
Beckwith-wiedemann Syndrome
Malignant Paraganglionic Neoplasm
Nephroblastoma
Malignant Neoplasms
Neoplasms

Liver Neoplasms
Mammary Neoplasms
Hepatoblastoma

Pathways

Methylation
Translation
Localization

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/SLC22A18AS

References

PMID: 9570947 by Cooper P.R., et al. Divergently transcribed overlapping genes expressed in liver and kidney and located in the 11p15.5 imprinted domain.

PMID: 9520460 by Schwienbacher C., et al. Transcriptional map of 170-kb region at chromosome 11p15.5: identification and mutational analysis of the BWR1A gene reveals the presence of mutations in tumor samples.