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Mouse Anti-SFTPC Recombinant Antibody (CBT3290) (V2LY-0625-LY2787)


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Tested Data
Mouse Anti-SFTPC Recombinant Antibody (CBT3290) (V2LY-0625-LY2787) in WB
Mouse Anti-SFTPC Recombinant Antibody (CBT3290) (V2LY-0625-LY2787) in WB
Mouse Anti-SFTPC Recombinant Antibody (CBT3290) (V2LY-0625-LY2787) in WB
Mouse Anti-SFTPC Recombinant Antibody (CBT3290) (V2LY-0625-LY2787) in WB
Mouse Anti-SFTPC Recombinant Antibody (CBT3290) (V2LY-0625-LY2787) in ELISA
Mouse Anti-SFTPC Recombinant Antibody (CBT3290) (V2LY-0625-LY2787) in ELISA

Summary

Host Animal
Mouse
Specificity
Human
Clone
CBT3290
Antibody Isotype
IgG1
Application
WB

Basic Information

Immunogen
Purified recombinant fragment of human SFTPC (AA: 60-180 ) expressed in E. Coli.
Host Species
Mouse
Specificity
Human
Antibody Isotype
IgG1
Clonality
Monoclonal Antibody
Application Notes
ApplicationNote
WB1:500-1:2,000
ELISA1:10,000

Formulations & Storage [For reference only, actual COA shall prevail!]

Format
Liquid
Buffer
PBS
Preservative
Sodium azide
Concentration
Batch dependent
Purity
> 95% Purity determined by SDS-PAGE.
Storage
Store at +4°C short term (1-2 weeks). Aliquot and store at -20°C long term. Avoid repeated freezethaw cycles.

Target

Full Name
Surfactant Protein C
Entrez Gene ID
6440
Function
Pulmonary surfactant associated proteins promote alveolar stability by lowering the surface tension at the air-liquid interface in the peripheral air spaces.
Biological Process
Respiratory gaseous exchange by respiratory system
Cellular Location
Secreted, extracellular space, surface film
Involvement in disease
Pulmonary surfactant metabolism dysfunction 2 (SMDP2):
A rare disease associated with progressive respiratory insufficiency and lung disease with a variable clinical course, due to impaired surfactant homeostasis. It is characterized by alveolar filling with floccular material that stains positive using the periodic acid-Schiff method and is derived from surfactant phospholipids and protein components. Excessive lipoproteins accumulation in the alveoli results in severe respiratory distress.
Respiratory distress syndrome in premature infants (RDS):
A lung disease affecting usually premature newborn infants. It is characterized by deficient gas exchange, diffuse atelectasis, high-permeability lung edema and fibrin-rich alveolar deposits called 'hyaline membranes'.
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For research use only. Not intended for any clinical use.

Custom Antibody Labeling

We also offer labeled antibodies developed using our catalog antibody products and nonfluorescent conjugates (HRP, AP, Biotin, etc.) or fluorescent conjugates (Alexa Fluor, FITC, TRITC, Rhodamine, Texas Red, R-PE, APC, Qdot Probes, Pacific Dyes, etc.).

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