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OSTM1 Human Recombinant Protein

For Research Use Only. Not for use in diagnostic procedures. Catalog #: MBS2546014

Background: Osteopetrosis-associated transmembrane protein 1 (OSTM1) is a Single-pass type I  membrane protein. It is expressed in many hematopoietic cells of the myeloid and lymphoid B- and T-lineages. The analysis of OSTM1 association with CLCN7… More details

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Product Overview

Online Datasheet in PDF
Product Name
OSTM1, Recombinant Protein
Full Product Name
Recombinant Human OSTM1 Protein (His tag)
Product Gene Name
Product Synonym Names
GIPN, GL, HSPC019, OPTB5, OSTM1
Host
Human Cells
Form/Format
Lyophilized from sterile PBS, pH 7.4
Purity/Purification
> 97 % as determined by SDS-PAGE
Preparation and Storage
Samples are stable for up to twelve months from date of receipt at -70 degree C
Molecular Weight
37,257 Da
OMIM
AF533891 mRNA
3D Structure
ModBase 3D Structure for Q86WC4
Predicted N Terminal
Ala 32
Endotoxin
< 1.0 EU per mug of the protein as determined by the LAL method
ISO Certification
Manufactured in an ISO 9001:2015 Certified Laboratory.
Application Notes for OSTM1 recombinant protein
The recombinant human OSTM1 comprises 264 amino acids and has a calculated molecular mass of 29.7 kDa. As a result of glycosylation, the recombinant protein migrates as an approximately 40-50 kDa protein in SDS-PAGE under reducing conditions.

Other Notes

Small volumes of OSTM1 recombinant protein 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.

Searchable Terms for OSTM1 purchase

MBS2546014 is a recombinant protein targeting OSTM1. Also known as Recombinant Human OSTM1 Protein (His tag). Host: Human Cells.

Additional Details

NCBI/Uniprot data below describe general gene information for OSTM1. It may not necessarily be applicable to this product.

NCBI GI #
NCBI GeneID
NCBI Accession #
UniProt Primary Accession #
UniProt Secondary Accession #
UniProt Related Accession #
GenBank Nucleotide #
NCBI Official Full Name
osteopetrosis-associated transmembrane protein 1
NCBI Official Synonym Full Names
osteopetrosis associated transmembrane protein 1
NCBI Official Symbol
OSTM1
NCBI Official Synonym Symbols
GL; GIPN; OPTB5; HSPC019
UniProt Protein Name
Osteopetrosis-associated transmembrane protein 1
UniProt Synonym Protein Names
Chloride channel 7 beta subunit
UniProt Gene Name
OSTM1
UniProt Synonym Gene Names
GL
NCBI Protein Information
osteopetrosis-associated transmembrane protein 1

NCBI Summary for OSTM1

This gene encodes a protein that may be involved in the degradation of G proteins via the ubiquitin-dependent proteasome pathway. The encoded protein binds to members of subfamily A of the regulator of the G-protein signaling (RGS) family through an N-terminal leucine-rich region. This protein also has a central RING finger-like domain and E3 ubiquitin ligase activity. This protein is highly conserved from flies to humans. Defects in this gene may cause the autosomal recessive, infantile malignant form of osteopetrosis. [provided by RefSeq, Jul 2008]
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UniProt Comments for OSTM1

OSTM1: Required for osteoclast and melanocyte maturation and function. Defects in OSTM1 are the cause of osteopetrosis autosomal recessive type 5 (OPTB5); also called infantile malignant osteopetrosis 3. Osteopetrosis is a rare genetic disease characterized by abnormally dense bone, due to defective resorption of immature bone. The disorder occurs in two forms: a severe autosomal recessive form occurring in utero, infancy, or childhood, and a benign autosomal dominant form occurring in adolescence or adulthood. OPTB5 patients manifest primary central nervous system involvement in addition to the classical stigmata of severe bone sclerosis, growth failure, anemia, thrombocytopenia and visual impairment with optic atrophy.

Protein type: EC 6.3.2.-; Ligase; Membrane protein, integral; Ubiquitin conjugating system; Ubiquitin ligase

Chromosomal Location of Human Ortholog: 6q21

Cellular Component: cytoplasm; intracellular membrane-bound organelle; lysosomal membrane; nucleus

Disease: Osteopetrosis, Autosomal Recessive 5
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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.

Product Note

Select online data sheet information is drawn from bioinformatics databases, occasionally resulting in ambiguous or non-relevant product information. It is the responsibility of the customer to review, verify, and evaluate the information to make sure it matches their requirements before purchasing the kit. Our ELISA Kit assays are dynamic research tools and sometimes they may be updated and improved. If the format of this assay is important to you then please request the current manual or contact our technical support team with a presales inquiry before placing an order. We will confirm the current details of the assay. We cannot guarantee the sample manual posted online is the most current manual, it is intended to serve as an example only. Please refer to the instructions For Use provided with the assay kit for precise details.

Product PubMed Publications

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