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MIPOL1 Antibody – Rabbit Polyclonal

For Research Use Only. Not for use in diagnostic procedures. Catalog #: MBS6320893

This gene encodes a coiled-coil domain-containing protein. The encoded protein may function as a tumor suppressor. A translocation that results in truncation of the protein encoded by this locus has been associated with mirror-image polydactyly, also known as… More details

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Testing Data View PDF
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Technical Datasheet View PDF
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Product Overview

Online Datasheet in PDF
Product Name
MIPOL1, Polyclonal Antibody
Full Product Name
MIPOL1, ID (Mirror-image polydactyly gene 1 protein,MIPOL1,) (MaxLight 405)
Product Gene Name
Product Synonym Names
Mirror-image polydactyly gene 1 protein,MIPOL1
Clonality
Polyclonal
Isotype
IgG
Host
Rabbit
Species Reactivity
Human
Form/Format
Supplied as a liquid in PBS, pH 7.2. No preservative added. Labeled with MaxLight405.
Purity/Purification
Purified by Protein A Affinity Chromatography.
Preparation and Storage
Store product at 4 degree C in the dark. DO NOT FREEZE! Stable at 4 degree C for 12 months after receipt as an undiluted liquid. Dilute required amount only prior to immediate use. Further dilutions can be made in assay buffer. Caution: MaxLight405 conjugates are sensitive to light. For maximum recovery of product, centrifuge the original vial prior to removing the cap.
Molecular Weight
19,900 Da
OMIM
606850
3D Structure
ModBase 3D Structure for Q8TD10
Immunogen
MIPOL1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 117-147 amino acids from the Central region of human MIPOL1.
Conjugate
MaxLight405
Note
Preservative Free

Product Categories/Family for anti-MIPOL1 antibody

Applications Tested/Suitable for anti-MIPOL1 antibody
Western Blot (WB), FLISA
Application Notes for anti-MIPOL1 antibody
WB: 1:100-500
FLISA: 1:1,000
Applications are based on unconjugated antibody.

Product References and Citations for anti-MIPOL1 antibody

Cheung, A.K., et al. Proc. Natl. Acad. Sci. U.S.A. 106(34):14478-14483(2009). Kamnasaran, D., et al. Eur. J. Hum. Genet. 11(4):315-324(2003). Kondoh, S., et al. J. Hum. Genet. 47(3):136-139(2002).

Other Notes

Small volumes of anti-MIPOL1 antibody 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 MIPOL1 purchase

MBS6320893 is an antibody targeting MIPOL1. Also known as MIPOL1, ID (Mirror-image polydactyly gene 1 protein,MIPOL1,) (MaxLight 405). Reactive in Human. Host: Rabbit.

Additional Details

NCBI/Uniprot data below describe general gene information for MIPOL1. It may not necessarily be applicable to this product.

NCBI GI #
NCBI GeneID
NCBI Accession #
NCBI Related Accession #
UniProt Primary Accession #
UniProt Secondary Accession #
UniProt Related Accession #
GenBank Nucleotide #
NCBI Official Full Name
mirror-image polydactyly gene 1 protein
NCBI Official Synonym Full Names
mirror-image polydactyly 1
NCBI Official Symbol
MIPOL1
UniProt Protein Name
Mirror-image polydactyly gene 1 protein
UniProt Gene Name
MIPOL1
UniProt Entry Name
MIPO1_HUMAN
NCBI Protein Information
mirror-image polydactyly gene 1 protein

UniProt Comments for MIPOL1

MIPOL1: A chromosomal aberration involving MIPOL1 is found in a patient with mirror-image polydactyly of hands and feet without other anomalies (MIP). Translocation t(2;14)(p23.3;q13). MIP is a very rare congenital anomaly characterized by mirror- image duplication of digits. MIP is occasionally associated with dimelia of the ulna and fibula, tibial and/or fibular hypoplasia, nasal abnormality and other malformations. Most MIP cases are sporadic, but very rare parent-child transmissions observed in familial cases suggest an autosomal mode of inheritance. 3 isoforms of the human protein are produced by alternative splicing.

Protein type: Unknown function

Chromosomal Location of Human Ortholog: 14q13.3

Cellular Component: nucleus

Disease: Laurin-sandrow Syndrome
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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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