FAM91A1 antibody (AA 335-440) (AbBy Fluor® 350)

Catalog No. ABIN896706

The AbBy Fluor® 350-conjugated Rabbit Polyclonal anti-FAM91A1 antibody (ABIN896706) specifically detects FAM91A1 in WB, IF (cc) and IF (p). The antibody is reactive with Human samples.

Quick Overview for FAM91A1 antibody (AA 335-440) (AbBy Fluor® 350) (ABIN896706)

Target: FAM91A1 (Family with Sequence Similarity 91, Member A1 (FAM91A1))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This FAM91A1 antibody is conjugated to AbBy Fluor® 350

Application: Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Product Details anti-FAM91A1 Antibody (AbBy Fluor® 350)

Binding Specificity: AA 335-440

Predicted Reactivity: Human,Mouse,Rat,Chicken

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human FAM91A1

Isotype: IgG

Application Details

Application Notes: 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 FAM91A1

Target: FAM91A1 (Family with Sequence Similarity 91, Member A1 (FAM91A1))

Alternative Name: FAM91A1

Background:

Synonyms: FAM91A1, Family with sequence similarity 91 member A1, FLJ23790, Hypothetical protein LOC157769, LOC157769, F91A1_HUMAN.

Background: Made up of nearly 146 million bases, chromosome 8 encodes about 800 genes. Translocation of portions of chromosome 8 with amplifications of the c-Myc gene are found in some leukemias and lymphomas, and typically associated with a poor prognosis. Portions of chromosome 8 have been linked to schizophrenia and bipolar disorder. Trisomy 8, also known as Warkany syndrome 2, most often results in early miscarriage but is occasionally seen in a mosaic form in surviving patients who suffer to a varying degree from a number of symptoms including retarded mental and motor development, and certain facial and developmental defects. WRN is a DNA helicase encoded by chromosome 8 and shown defective in those with the early aging disorder Werner syndrome. Chromosome 8 is also associated with Pfeiffer syndrome, congenital hypothyroidism and Waardenburg syndrome. The FAM91A1 gene product has been provisionally designated FAM91A1 pending further characterization.

Gene ID: 157769