FSIP1 antibody (AA 101-200) (AbBy Fluor® 680)
-
- Target See all FSIP1 Antibodies
- FSIP1 (Fibrous Sheath Interacting Protein 1 (FSIP1))
-
Binding Specificity
- AA 101-200
-
Reactivity
- Rat
-
Host
- Rabbit
-
Clonality
- Polyclonal
-
Conjugate
- This FSIP1 antibody is conjugated to AbBy Fluor® 680
-
Application
- Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- Cross-Reactivity
- Rat
- Predicted Reactivity
- Human,Mouse,Dog,Cow,Sheep
- Purification
- Purified by Protein A.
- Immunogen
- KLH conjugated synthetic peptide derived from human FSIP1
- Isotype
- IgG
- Top Product
- Discover our top product FSIP1 Primary Antibody
-
-
- Application Notes
-
IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200 - Restrictions
- For Research Use only
-
- 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
- FSIP1 (Fibrous Sheath Interacting Protein 1 (FSIP1))
- Alternative Name
- FSIP1 (FSIP1 Products)
- Synonyms
- zgc:113106 antibody, 1700012M13Rik antibody, 4933432K11Rik antibody, fibrous sheath interacting protein 1 antibody, fibrous sheath-interacting protein 1 antibody, FSIP1 antibody, Fsip1 antibody, fsip1 antibody
- Background
-
Synonyms: Fibrous sheath interacting protein 1, FLJ35989, HSD10, FSIP1_HUMAN.
Background: FSIP1 is a 581 amino acid protein that is expressed in airway epithelium. A member of the FSIP1 family, FSIP1 is encoded by a gene that maps to human chromosome 15q14 and mouse chromosome 2 E5. Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is about 3 % of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene.
- Gene ID
- 161835
-