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Rabbit Anti-FA20A antibody
Rabbit Anti-FA20A antibody
FA20A_HUMAN; Protein FAM20A.
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  • NO.:SL13619R
    Clonality:Polyclonal
    Immunogen Species:Rabbit
    React Species:Human,Mouse,(predicted: Rat,Rabbit,)
    Applications:WB ELISA IHC-P IHC-F ICC IF
    concentration:1mg/ml
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Details

Product Name FA20A
Chinese Name FA20A抗体
Alias FA20A_HUMAN; Protein FAM20A.  
Research Area Cell biology  Stem cells  Cell differentiation  
Immunogen Species Rabbit
Clonality Polyclonal
React Species Human, Mouse,  (predicted: Rat, Rabbit, )
Applications WB=1:500-2000 ELISA=1:5000-10000 IHC-P=1:100-500 IHC-F=1:100-500 ICC=1:100-500 IF=1:100-500 (Paraffin sections need antigen repair)
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
Theoretical molecular weight 57kDa
Cellular localization cytoplasmic 
Form Liquid
Concentration 1mg/ml
immunogen KLH conjugated synthetic peptide derived from human FA20A: 101-200/541 
Lsotype IgG
Purification affinity purified by Protein A
Buffer Solution 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
Storage Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
Attention This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
Product Detail FA20A belongs to the FAM20 family. All FAM20 proteins contain putative conserved signal sequences as well as a conserved C terminal domain. FA20A is a secreted glycoprotein. It has been found in EML and MPRO cell lines, with low levels in undifferentiated cells. FA20A is induced during maturation to promyelocyte stage of neutrophil differentiation and decreased during neutrophil terminal differentiation.

Subcellular Location:
Secreted

Tissue Specificity:
Highly expressed in lung and liver. Intermediate levels in thymus and ovary.

Post-translational modifications:
N-glycosylated (By similarity).

DISEASE:
Amelogenesis imperfecta and gingival fibromatosis syndrome (AIGFS) [MIM:614253]: 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. Note=The disease is caused by mutations affecting the gene represented in this entry.

Similarity:
Belongs to the FAM20 family.

SWISS:
Q96MK3

Gene ID:
54757

Database links:

Entrez Gene: 54757 Human

Omim: 611062 Human

SwissProt: Q96MK3 Human

Unigene: 268874 Human



Product Picture
Sample: Lung(Mouse) Lysate at 40 ug
Primary: Anti-FA20A(SL10196R) at 1/300 dilution
Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution
Predicted band size: 57 kD
Observed band size: 57 kD
Sample: MDA-MB-231 (human)Cell Lysate at 40 ug
Primary: Anti-FA20A(SL13619R) at 1/300 dilution
Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution
Predicted band size: 57 kD
Observed band size: 57kD
FA20A

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