FAM83F antibody (AA 261-360)

Catalog No. ABIN1385891

The Rabbit Polyclonal anti-FAM83F antibody has been validated for WB, ELISA, ICC, IF (cc), IF (p), IHC (fro) and IHC (p). It is suitable to detect FAM83F in samples from Mouse.

Quick Overview for FAM83F antibody (AA 261-360) (ABIN1385891)

Target: FAM83F (Family with Sequence Similarity 83, Member F (FAM83F))

Reactivity: Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This FAM83F antibody is un-conjugated

Application: Western Blotting (WB), ELISA, Immunocytochemistry (ICC), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Product Details anti-FAM83F Antibody

Binding Specificity: AA 261-360

Cross-Reactivity: Mouse

Predicted Reactivity: Human,Rat,Cow,Pig

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human FAM83F

Isotype: IgG

Application Details

Application Notes: WB 1:300-5000
ELISA 1:500-1000
IHC-P 1:200-400
IHC-F 1:100-500
IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200
ICC 1:100-500

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 μg/μL

Buffer: 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % 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: 4 °C,-20 °C

Storage Comment: Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.

Expiry Date: 12 months

Target Details for FAM83F

Target: FAM83F (Family with Sequence Similarity 83, Member F (FAM83F))

Alternative Name: FAM83F

Background:

Synonyms: Family with sequence similarity 83 member F, Hypothetical protein LOC113828, RP3 496C20.4, FA83F_HUMAN.

Background: Chromosome 22 contains over 500 genes and about 49 million bases. Being the second smallest human chromosome, 22 contains a surprising variety of interesting genes. Phelan-McDermid syndrome, Neurofibromatosis type 2 and autism are associated with chromosome 22. A schizophrenia susceptibility locus has been identified on chromosome 22 and studies show that 22q11 deletion symptoms include a high incidence of schizophrenia. Translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia Chromosome and the subsequent production of the novel fusion protein, BCR-Abl, a potent cell proliferation activator found in several types of leukemia. The FAM83F gene product has been provisionally designated FAM83F pending further characterization.

Gene ID: 113828