FHAD1 antibody (AA 401-500)

Catalog No. ABIN1714364

The Rabbit Polyclonal anti-FHAD1 antibody has been validated for IF (cc), IF (p), ELISA, IHC (p), IHC (fro) and ICC. It is suitable to detect FHAD1 in samples from Human.

Quick Overview for FHAD1 antibody (AA 401-500) (ABIN1714364)

Target: FHAD1 (Forkhead-Associated (FHA) Phosphopeptide Binding Domain 1 (FHAD1))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This FHAD1 antibody is un-conjugated

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

Product Details anti-FHAD1 Antibody

Binding Specificity: AA 401-500

Predicted Reactivity: Human,Mouse,Rat,Cow,Sheep,Rabbit

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human FHAD1

Isotype: IgG

Application Details

Application Notes: 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 FHAD1

Target: FHAD1 (Forkhead-Associated (FHA) Phosphopeptide Binding Domain 1 (FHAD1))

Alternative Name: FHAD1

Background:

Synonyms: FHA domain-containing protein 1, Forkhead-associated FHA phosphopeptide binding domain, Forkhead-associated domain-containing protein 1, KIAA1937, RP3-467K16.1, FHAD1_HUMAN.

Background: The FHAD1 gene encodes a 1,420 amino acid protein and maps to human chromosome 1, the largest human chromosome which spans about 260 million base pairs and makes up 8 % of the human genome. Other notable genes located on chromosome 1 include LMNA, which is associated with the rare aging disease Hutchinson-Gilford progeria, and the MUTYH gene, which is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma.

Gene ID: 114827