FAM98A antibody (AA 251-350) (Cy5)

Catalog No. ABIN1406650

Product Details anti-FAM98A Antibody (Cy5)

Target: FAM98A (Family with Sequence Similarity 98, Member A (FAM98A))

Binding Specificity: AA 251-350

Reactivity: Human, Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This FAM98A antibody is conjugated to Cy5

Application: Flow Cytometry (FACS), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Cross-Reactivity: Human, Mouse

Predicted Reactivity: Rat,Cow,Sheep,Pig,Horse,Chicken

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human FAM98A

Isotype: IgG

Application Details

Application Notes: FCM 1:20-100
IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

Preservative: ProClin

Precaution of Use: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

Storage: -20 °C

Storage Comment: Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Expiry Date: 12 months

Target Details for FAM98A

Target: FAM98A (Family with Sequence Similarity 98, Member A (FAM98A))

Alternative Name: FAM98A (FAM98A Products)

Synonyms: 2810405J04Rik antibody, AL024114 antibody, RGD1305486 antibody, family with sequence similarity 98 member A antibody, family with sequence similarity 98, member A antibody, FAM98A antibody, Fam98a antibody

Background:

Synonyms: FAM 98A, Family with sequence similarity 98 member A, Hypothetical protein LOC25940, LOC25940, Protein FAM98A, FA98A_HUMAN.

Background: Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is about 3 % of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene. The FAM98 gene product has been provisionally designated FAM98 pending further characterization.

Gene ID: 25940

Pathways: SARS-CoV-2 Protein Interactome