Mouse Anti-FAM50A Recombinant Antibody (CBXF-0279) (V2LY-0825-LY1349)

Name: Mouse Anti-FAM50A Recombinant Antibody (CBXF-0279)
SKU: V2LY-0825-LY1349
Rating: 5 (1 reviews)

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Datasheet

SDS

Request for COA

Datasheet Target References Q & As Review & reward Protocols Associated Products

Basic Information

Host Animal

Mouse

Clone

CBXF-0279

Application

WB, IP, IF, ELISA, IHC-P

Immunogen

Amino acids 318-339 of human FAM50A.

Host Species

Mouse

Specificity

Human, Mouse, Rat

Antibody Isotype

IgG2b, κ

Clonality

Monoclonal Antibody

Application Notes

Application	Note
ELISA	1:100-1:1,000
WB	1:100-1:1,000
IP	1-2 µg per 100-500 µg of total protein (1 ml of cell lysate)
IF(ICC)	1:50-1:500
IHC-P	1:50-1:500

Formulations & Storage [For reference only, actual COA shall prevail!]

Format

Liquid

Buffer

PBS, gelatin

Preservative

Sodium azide

Concentration

0.2 mg/ml

Purity

> 95% Purity determined by SDS-PAGE.

Storage

Store at +4°C short term (1-2 weeks). Aliquot and store at -20°C long term. Avoid repeated freezethaw cycles.

More Infomation

Target

Full Name

family with sequence similarity 50, member A

Entrez Gene ID

Human	9130
Mouse	108160
Rat	293862

UniProt ID

Human	Q14320
Mouse	Q9WV03
Rat	B5DF16

Research Area

Probably involved in the regulation of pre-mRNA splicing.

Biological Process

Chromatin organization Source: GO_Central
mRNA processing Source: UniProtKB-KW
Regulation of RNA splicing Source: UniProtKB
RNA splicing Source: UniProtKB-KW
Spermatogenesis Source: UniProtKB

Cellular Location

Nucleus

Involvement in disease

Intellectual developmental disorder, X-linked, syndromic, Armfield type (MRXSA):
An X-linked recessive disorder characterized by global developmental delay with impaired intellectual development, walking difficulties and poor or absent speech. Affected individuals display a distinctive phenotype characterized by postnatal growth retardation, variable head circumference with a prominent forehead and dysmorphic facial features, ocular abnormalities, and seizures.

Lee, Y. R., Khan, K., Armfield-Uhas, K., Srikanth, S., Thompson, N. A., Pardo, M., ... & Schwartz, C. E. (2020). Mutations in FAM50A suggest that Armfield XLID syndrome is a spliceosomopathy. Nature communications, 11(1), 1-17.

Kim, Y., Hur, S. W., Jeong, B. C., Oh, S. H., Hwang, Y. C., Kim, S. H., & Koh, J. T. (2018). The Fam50a positively regulates ameloblast differentiation via interacting with Runx2. Journal of Cellular Physiology, 233(2), 1512-1522.

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Please try the standard protocols which include: protocols, troubleshooting and guide.

Enzyme-linked Immunosorbent Assay (ELISA)
Flow Cytometry
Immunofluorescence (IF)
Immunohistochemistry (IHC)
Immunoprecipitation (IP)
Western Blot (WB)
Enzyme Linked Immunospot (ELISpot)
Proteogenomic
Other Protocols

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Mouse Anti-FAM50A Recombinant Antibody (CBXF-0278) (CAT#: CBMAB-F0275-CQ)

Rabbit Anti-FAM50A Recombinant Antibody (CBXF-1106) (CAT#: CBMAB-F0792-CQ)

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Isotype control

For research use only. Not intended for any clinical use.

Custom Antibody Labeling

We also offer labeled antibodies developed using our catalog antibody products and nonfluorescent conjugates (HRP, AP, Biotin, etc.) or fluorescent conjugates (Alexa Fluor, FITC, TRITC, Rhodamine, Texas Red, R-PE, APC, Qdot Probes, Pacific Dyes, etc.).

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