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anti-FAM20A antibody :: Rabbit anti-Human Family With Sequence Similarity 20 Polyclonal Antibody

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Catalog # MBS2026377 (SPECIAL PROMOTION: Get FREE $5 Starbucks gift card (Maximum 5 gift cards/product). Gift card(s) will be included with shipment)
Unit / Price
Scan QR to view Datasheet
  0.01 mg  /  $110 +1 FREE 8GB USB
  0.02 mg  /  $130 +1 FREE 8GB USB
  0.05 mg  /  $175 +1 FREE 8GB USB
  0.1 mg  /  $225 +1 FREE 8GB USB
  0.2 mg  /  $340 +1 FREE 8GB USB
  1 mg  /  $800 +1 FREE 8GB USB
Product Name

Family With Sequence Similarity 20 (FAM20A), Polyclonal Antibody

Full Product Name

Polyclonal Antibody to Family With Sequence Similarity 20, Member A (FAM20A)

Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
OMIM
AK056789 mRNA
3D Structure
ModBase 3D Structure for Q96MK3
Clonality
Polyclonal
Isotype
IgG
Host
Rabbit
Species Reactivity
Human
Specificity
The antibody is a rabbit polyclonal antibody raised against FAM20A. It has beenselected for its ability to recognize FAM20A in immunohistochemical staining andwestern blotting.
Purity/Purification
Affinity Chromatography
Form/Format
Liquid
Concentration
200ug/ml (lot specific)
Fragment
FAM20A (Lys368~Ser541)
Organism Species
Homo sapiens (Human)
Conjugate
No Conjugate
Immunogen
Recombinant FAM20A (Lys368~Ser541) expressed in E Coli.
Conjugated Antibody
The APC conjugated antibody version of this item is also available as catalog #MBS2082248
Preparation and Storage
Store at 4 degree C for frequent use. Stored at -20 degree C to -80 degree C in a manual defrost freezer for one year without detectable loss of activity. Avoid repeated freeze-thaw cycles.
ISO Certification
Manufactured in an ISO 9001:2008 and ISO 13485:2003 Certified Laboratory.
Supply Chain Verification
Manufactured in a lab with traceable raw materials. Bulk orders can typically be prepared to the customer’s specifications, please inquire.
Other Notes
Small volumes of anti-FAM20A 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.
Applications Tested/Suitable for anti-FAM20A antibody
Western Blot (WB), Immunocytochemistry (ICC), Immunohistochemistry (IHC) Formalin/Paraffin, ELISA (EIA)
Application Notes for anti-FAM20A antibody
Western blotting: 0.2-2ug/mL;1:250-2500
Immunohistochemistry: 5-20ug/mL;1:25-100
Immunocytochemistry: 5-20ug/mL;1:25-100
Optimal working dilutions must be determined by end user.

Western Blot (WB) of anti-FAM20A antibody
Western Blot: Sample: Recombinant protein.
anti-FAM20A antibody Western Blot (WB) (WB) image
Immunohistochemistry (IHC) of anti-FAM20A antibody
DABstainingonIHC-P.Samples:HumanTissue)
anti-FAM20A antibody Immunohistochemistry (IHC) (IHC) image
NCBI/Uniprot data below describe general gene information for FAM20A. It may not necessarily be applicable to this product.
NCBI GI #
NCBI GeneID
NCBI Accession #
NCBI GenBank Nucleotide #
UniProt Primary Accession #
UniProt Secondary Accession #
UniProt Related Accession #
Molecular Weight
61,417 Da
NCBI Official Full Name
pseudokinase FAM20A isoform b
NCBI Official Synonym Full Names
FAM20A, golgi associated secretory pathway pseudokinase
NCBI Official Symbol
FAM20A  [Similar Products]
NCBI Official Synonym Symbols
AI1G; AIGFS; FP2747
  [Similar Products]
NCBI Protein Information
pseudokinase FAM20A
UniProt Protein Name
Pseudokinase FAM20A
Protein Family
UniProt Gene Name
FAM20A  [Similar Products]
NCBI Summary for FAM20A
This locus encodes a protein that is likely secreted and may function in hematopoiesis. A mutation at this locus has been associated with amelogenesis imperfecta and gingival hyperplasia syndrome. Alternatively spliced transcript variants have been identified. [provided by RefSeq, Aug 2011]
UniProt Comments for FAM20A
FAM20A: Defects in FAM20A are the cause of amelogenesis imperfecta and gingival fibromatosis syndrome (AIGFS). An autosomal recessive condition characterized by mild gingival fibromatosis and dental anomalies, including hypoplastic amelogenesis imperfecta, intrapulpal calcifications, delay of tooth eruption, hypodontia/oligodontia, pericoronal radiolucencies, and unerupted teeth. Belongs to the FAM20 family.

Protein type: Secreted; Secreted, signal peptide

Chromosomal Location of Human Ortholog: 17q24.2

Cellular Component: cell; endoplasmic reticulum; extracellular space; Golgi apparatus

Molecular Function: protein binding; protein serine/threonine kinase activator activity; protein serine/threonine kinase activity

Biological Process: biomineral formation; calcium ion homeostasis; positive regulation of protein phosphorylation

Disease: Amelogenesis Imperfecta, Type Ig
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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