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OCA2, Blocking Peptide

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產(chǎn)品名稱: OCA2, Blocking Peptide
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OCA2, Blocking Peptide


OCA2, Blocking Peptide  的詳細(xì)介紹
Product Name

OCA2, Blocking Peptide

Full Product Name

OCA2 Antibody (N-Term) Blocking peptide

Product Synonym Names
P protein; Melanocyte-specific transporter protein; Pink-eyed dilution protein homolog; OCA2; D15S12; P
Product Gene Name

OCA2 blocking peptide

[Similar Products]
Product Synonym Gene Name
D15S12; P[Similar Products]
Antibody/Peptide Pairs
OCA2 peptide (MBS9217478) is used for blocking the activity of OCA2 antibody (MBS9204399)
Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
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OMIM
203200
3D Structure
ModBase 3D Structure for Q04671
Form/Format
Synthetic peptide was lyophilized with 100% acetonitrile and is supplied as a powder. Reconstitute with 0.1 ml DI water for a final concentration of 1 mg/ml.
Cellular Location
Melanosome membrane; Multi-pass membrane protein
Preparation and Storage
Maintain refrigerated at 2-8 degree C for up to 6 months. For long term storage store at -20 degree C.
Other Notes
Small volumes of OCA2 blocking peptide vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.
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Related Product Information for
OCA2 blocking peptide
Could be involved in the transport of tyrosine, the precursor to melanin synthesis, within the melanocyte. Regulates the pH of melanosome and the melanosome maturation. One of the components of the mammalian pigmentary system. Seems to regulate the post-translational processing of tyrosinase, which catalyzes the limiting reaction in melanin synthesis. May serve as a key control point at which ethnic skin color variation is determined. Major determinant of brown and/or blue eye color.
NCBI/Uniprot data below describe general gene information for OCA2. It may not necessarily be applicable to this product.
NCBI GI #
157266326
NCBI GeneID
4948
NCBI Accession #
NP_000266.2 [Other Products]
NCBI GenBank Nucleotide #
NM_000275.2 [Other Products]
UniProt Primary Accession #
Q04671 [Other Products]
UniProt Secondary Accession #
Q15211; Q15212; Q96EN1; Q9UMI5[Other Products]
UniProt Related Accession #
Q04671[Other Products]
Molecular Weight
74,312 Da
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NCBI Official Full Name
P protein isoform 1
NCBI Official Synonym Full Names
OCA2 melanosomal transmembrane protein
NCBI Official Symbol
OCA2??[Similar Products]
NCBI Official Synonym Symbols
P; BEY; PED; BEY1; BEY2; BOCA; EYCL; HCL3; EYCL2; EYCL3; SHEP1; D15S12
??[Similar Products]
NCBI Protein Information
P protein
UniProt Protein Name
P protein
UniProt Synonym Protein Names
Melanocyte-specific transporter protein; Pink-eyed dilution protein homolog
Protein Family
P protein
UniProt Gene Name
OCA2??[Similar Products]
UniProt Synonym Gene Names
D15S12; P??[Similar Products]
UniProt Entry Name
P_HUMAN
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NCBI Summary for OCA2
This gene encodes the human homolog of the mouse p (pink-eyed dilution) gene. The encoded protein is believed to be an integral membrane protein involved in small molecule transport, specifically tyrosine, which is a precursor to melanin synthesis. It is involved in mammalian pigmentation, where it may control skin color variation and act as a determinant of brown or blue eye color. Mutations in this gene result in type 2 oculocutaneous albinism. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014]
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UniProt Comments for OCA2
OCA2: a transporer of tyrosine, a precursor for melanin synthesis, within melanocytes. Regulates the pH of melanosomes and melanosome maturation. One of the components of the mammalian pigmentary system. Seems to regulate the postranslational processing of tyrosinase, which catalyzes the limiting reaction in melanin synthesis. May serve as a key control point at which ethnic skin color variation is determined. Major determinant of brown and/or blue eye color. Belongs to the SLC13A transporter family.

Protein type: Membrane protein, integral; Membrane protein, multi-pass; Transporter

Chromosomal Location of Human Ortholog: 15q

Cellular Component: cytoplasm; endoplasmic reticulum membrane; endosome membrane; lysosomal membrane; melanosome membrane

Molecular Function: L-tyrosine transmembrane transporter activity; protein binding; transporter activity

Biological Process: eye pigment biosynthetic process

Disease: Albinism, Oculocutaneous, Type Ii; Skin/hair/eye Pigmentation, Variation In, 1
Research Articles on OCA2
1. Two nonsynonymous OCA2 polymorphisms (rs1800414 and rs74653330) are independently associated with normal skin pigmentation variation in East Asian populations and have very different frequency distributions in East Asia.
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Precautions
All of MyBioSource's Products are for scientific laboratory research purposes and are not for diagnostic, therapeutics, prophylactic or in vivo use. Through your purchase, you expressly represent and warrant to MyBioSource that you will properly test and use any Products purchased from MyBioSource in accordance with industry standards. MyBioSource and its authorized distributors reserve the right to refuse to process any order where we reasonably believe that the intended use will fall outside of our acceptable guidelines.
Disclaimer
While every efforts were made to ensure the accuracy of the information provided in this datasheet, MyBioSource will not be liable for any omissions or errors contained herein. MyBioSource reserves the right to make changes to this datasheet at any time without prior notice.

It is the responsibility of the customer to report product performance issues to MyBioSource within 30 days of receipt of the product. Please visit our Terms & Conditions page for more information.
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