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AICDA, Polyclonal Antibody

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產(chǎn)品名稱: AICDA, Polyclonal Antibody
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AICDA, Polyclonal Antibody


AICDA, Polyclonal Antibody  的詳細介紹
Product Name

AICDA, Polyclonal Antibody

Full Product Name

Mouse Aicda Polyclonal Antibody

Product Synonym Names
Aid; Activation-induced cytidine deaminase; Cytidine aminohydrolase; AID
Product Gene Name

anti-AICDA antibody

[Similar Products]
Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
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Clonality
Polyclonal
Isotype
IgG
Host
Rabbit
Species Reactivity
Human
Purity/Purification
Immunogen Affinity Purified
Form/Format
Liquid; 0.1MxPBS, 50% Glycerol, pH7.5
Concentration
200 ug/ml (lot specific)
Immunogen
Recombinant Human Aicda Protein
Preparation and Storage
Store at 4 degree C for frequent use. Store at -20 degree C to -70 degree C for 6 months.
Other Notes
Small volumes of anti-AICDA 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.
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Applications Tested/Suitable for anti-AICDA antibody
Western Blot (WB), Immunohistochemistry (IHC)
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NCBI/Uniprot data below describe general gene information for AICDA. It may not necessarily be applicable to this product.
NCBI GI #
53854920
NCBI GeneID
57379
UniProt Related Accession #
Q9GZX7[Other Products]
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NCBI Official Full Name
activation-induced deaminase, partial
NCBI Official Synonym Full Names
activation induced cytidine deaminase
NCBI Official Symbol
AICDA??[Similar Products]
NCBI Official Synonym Symbols
AID; ARP2; CDA2; HIGM2; HEL-S-284
??[Similar Products]
NCBI Protein Information
single-stranded DNA cytosine deaminase
Protein Family
Single-stranded DNA cytosine deaminase
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NCBI Summary for AICDA
This gene encodes a RNA-editing deaminase that is a member of the cytidine deaminase family. The protein is involved in somatic hypermutation, gene conversion, and class-switch recombination of immunoglobulin genes. Defects in this gene are the cause of autosomal recessive hyper-IgM immunodeficiency syndrome type 2 (HIGM2). [provided by RefSeq, Feb 2009]
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Research Articles on AICDA
1. miR-29b acts to silence premature AID expression in naive B cells.
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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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