Description
SFTPA1 Antibody | 18-957 | Gentaur UK, US & Europe Distribution
Host: Rabbit
Reactivity: Human, Mouse
Homology: N/A
Immunogen: A synthetic peptide of human SFTPA1
Research Area: Cell Cycle, Signal Transduction
Tested Application: WB
Application: WB: 1:500 - 1:1000
Specificiy: N/A
Positive Control 1: NCI-H460
Positive Control 2: NCI-H125
Positive Control 3: NIH/3T3
Positive Control 4: 3T3L1
Positive Control 5: Mouse intestine
Positive Control 6: N/A
Molecular Weight: Observed: 35kDa
Validation: N/A
Isoform: N/A
Purification: Affinity purification
Clonality: Polyclonal
Clone: N/A
Isotype: IgG
Conjugate: Unconjugated
Physical State: Liquid
Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
Concentration: N/A
Storage Condition: Store at -20˚C. Avoid freeze / thaw cycles.
Alternate Name: SFTPA1, surfactant, pulmonary-associated protein A1B, pulmonary-associated protein A1A, surfactant protein A1B, surfactant protein A1 variant AD' 6A4, surfactant protein A1 variant AD' 6A3, surfactant protein A1 variant AD' 6A2, surfactant protein A1 variant AD' 6A, surfactant protein A1 variant ACD' 6A4, surfactant protein A1 variant ACD' 6A3, surfactant protein A1 variant ACD' 6A2, surfactant protein A1 variant AB'D' 6A4, surfactant protein A1 variant AB'D' 6A3, surfactant protein A1 variant AB'D' 6A2, surfactant protein A1, SP-A1, SPA1, SP-A, SPA, SFTPA1B, SFTP1, pulmonary surfactant-associated protein A1, PSP-A, PSPA, PSAP, OTTHUMP00000019931, OTTHUMP00000019930, OTTHUMP00000019929, OTTHUMP00000019928, MGC198590, MGC133365, FLJ99559, FLJ79095, FLJ77898, FLJ61144, FLJ51913, FLJ50593, collectin-4, COLEC4, alveolar proteinosis protein, 35 kDa pulmonary surfactant-associated protein, SFTPA
User Note: Optimal dilutions for each application to be determined by the researcher.
BACKGROUND: This gene encodes a lung surfactant protein that is a member of a subfamily of C-type lectins called collectins. The encoded protein binds specific carbohydrate moieties found on lipids and on the surface of microorganisms. This protein plays an essential role in surfactant homeostasis and in the defense against respiratory pathogens. Mutations in this gene are associated with idiopathic pulmonary fibrosis. Alternate splicing results in multiple transcript variants.