FAM91A1 antibody (AA 335-440) (HRP)

Catalog No. ABIN896718

The HRP-conjugated Rabbit Polyclonal anti-FAM91A1 antibody (ABIN896718) specifically detects FAM91A1 in WB, ELISA, IHC (p) and IHC (fro). The antibody is reactive with Human samples.

Quick Overview for FAM91A1 antibody (AA 335-440) (HRP) (ABIN896718)

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

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This FAM91A1 antibody is conjugated to HRP

Application: Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))

Product Details anti-FAM91A1 Antibody (HRP)

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: WB 1:300-5000
IHC-P 1:200-400
IHC-F 1:100-500

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.

Handling Advice: Do NOT add Sodium Azide! Use of Sodium Azide will inhibit enzyme activity of horseradish peroxidase.

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