FHAD1 antibody (AA 401-500)
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- Target See all FHAD1 products
- FHAD1 (Forkhead-Associated (FHA) Phosphopeptide Binding Domain 1 (FHAD1))
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Binding Specificity
- AA 401-500
- Reactivity
- Human
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This FHAD1 antibody is un-conjugated
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Application
- ELISA, Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunocytochemistry (ICC)
- Predicted Reactivity
- Human,Mouse,Rat,Cow,Sheep,Rabbit
- Purification
- Purified by Protein A.
- Immunogen
- KLH conjugated synthetic peptide derived from human FHAD1
- Isotype
- IgG
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- Application Notes
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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
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- 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
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- Target
- FHAD1 (Forkhead-Associated (FHA) Phosphopeptide Binding Domain 1 (FHAD1))
- Alternative Name
- FHAD1 (FHAD1 Products)
- Synonyms
- 2900090M10Rik antibody, B230311F11 antibody, RGD1563444 antibody, forkhead associated phosphopeptide binding domain 1 antibody, forkhead-associated (FHA) phosphopeptide binding domain 1 antibody, FHAD1 antibody, Fhad1 antibody
- Background
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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
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