Slc45a2 Antibodies

AND Slc45a2 ELISA kits, Slc45a2 Proteins

Many biological assays use antibodies to detect Slc45a2, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with Slc45a2 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop Slc45a2 antibodies...

We validate the specificity of these antibodies to Slc45a2 by testing them on tissues known to express Slc45a2 positively and negatively. Browse below to find the Slc45a2 antibody that suites your experiment. We have 0 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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Slc45a2 Infographic by Boster Bio

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Slc45a2 Overview

Facts about Membrane-associated transporter protein.

Membrane-associated transporter protein (Slc45a2)

Melanocyte differentiation antigen. May transport substances needed for melanin biosynthesis (By similarity).

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Gene Information

Mouse
Gene Name:	Slc45a2
Uniprot:	P58355
Entrez:	22293

Family

Belongs to:

glycoside-pentoside-hexuronide (GPH) cation symporter transporter (TC 2.A.2) family

Alternative Names

AIM-1; AIM11A1; MATPmembrane associated transporter; Melanoma antigen AIM1; membrane-associated transporter protein; Protein AIM-1; SHEP5; Solute carrier family 45 member 2; solute carrier family 45, member 2; underwhite

Molecular Weight

Mass (kDA):
57.961 kDA

Genomic Context


Mouse

Location:	15 A1\|15 5.4 cM
Sequence:	15;

Tissue Specificity

Melanocytes, eyes, kidney and uterus.

Diseases

Albinism, Oculocutaneous
Albinism
Hypopigmentation Disorder
Melanoma
Malignant Neoplasms
Malignant Neoplasm Of Skin
Skin Neoplasms
Oculocutaneous Albinism Type 2
Hereditary Diseases
Nystagmus
Hermanski-pudlak Syndrome
Albinism, Ocular

Malignant Paraganglionic Neoplasm
Strabismus
Carcinoma
Photophobia
Dysequilibrium Syndrome
Cutaneous Melanoma
Basal Cell Carcinoma

Pathways

Pigmentation
Transport
Cell-cell Signaling
Response To Stress
Eye Pigmentation
Dna Methylation
Reflex
Methylation
Cytoskeleton Organization
Response To Uv

Cell Death
Pathogenesis
Eye Development
Secretion

PTMs

Methylation

Research Areas

Breast Cancer

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/Slc45a2

References

PMID: 11479596 by Fukamachi S., et al. Mutations in the gene encoding B, a novel transporter protein, reduce melanin content in medaka.

PMID: 11574907 by Newton J.M., et al. Mutations in the human orthologue of the mouse underwhite gene (uw) underlie a new form of oculocutaneous albinism, OCA4.