Rabbit Recombinant Monoclonal SCIN antibody. C-terminal. Suitable for WB, IHC-P and reacts with Mouse, Rat, Human samples. Cited in 2 publications.
pH: 7.2 - 7.4
Preservative: 0.01% Sodium azide
Constituents: 59% PBS, 40% Glycerol (glycerin, glycerine), 0.05% BSA
WB | IHC-P | |
---|---|---|
Human | Tested | Tested |
Mouse | Tested | Expected |
Rat | Tested | Expected |
Species | Dilution info | Notes |
---|---|---|
Species Mouse | Dilution info 1/1000 | Notes Perform heat-mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol. |
Species Rat | Dilution info 1/1000 | Notes - |
Species Human | Dilution info 1/1000 | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info 1/250 | Notes Perform heat-mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol. |
Species | Dilution info | Notes |
---|---|---|
Species Mouse, Rat | Dilution info Use at an assay dependent concentration. | Notes - |
Select an associated product type
Ca(2+)-dependent actin filament-severing protein that has a regulatory function in exocytosis by affecting the organization of the microfilament network underneath the plasma membrane (PubMed:26365202, PubMed:8547642). Severing activity is inhibited by phosphatidylinositol 4,5-bis-phosphate (PIP2) (By similarity). In vitro, also has barbed end capping and nucleating activities in the presence of Ca(2+). Required for megakaryocyte differentiation, maturation, polyploidization and apoptosis with the release of platelet-like particles (PubMed:11568009). Plays a role in osteoclastogenesis (OCG) and actin cytoskeletal organization in osteoclasts (By similarity). Regulates chondrocyte proliferation and differentiation (By similarity). Inhibits cell proliferation and tumorigenesis. Signaling is mediated by MAPK, p38 and JNK pathways (PubMed:11568009).
KIAA1905, SCIN, Scinderin, Adseverin
Rabbit Recombinant Monoclonal SCIN antibody. C-terminal. Suitable for WB, IHC-P and reacts with Mouse, Rat, Human samples. Cited in 2 publications.
pH: 7.2 - 7.4
Preservative: 0.01% Sodium azide
Constituents: 59% PBS, 40% Glycerol (glycerin, glycerine), 0.05% BSA
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
This product is a recombinant monoclonal antibody, which offers several advantages including:
For more information, read more on recombinant antibodies.
SCIN also known as scinderin or adseverin is an actin-severing protein involved in cytoskeletal dynamics. This protein has a mass of approximately 80 kDa. SCIN is expressed in a variety of tissues including neural hematopoietic and endocrine systems. Its mechanical function includes binding to filamentous actin and promoting severing which helps in the reorganization of the actin cytoskeleton. This activity is calcium-dependent making SCIN responsive to intracellular calcium levels.
SCIN influences cellular processes like secretion motility and division. SCIN belongs to the gelsolin/villin family of actin-modulating proteins and often acts within a protein complex to disassemble actin filaments. It regulates exocytosis by modulating actin dynamics near the plasma membrane especially in cells such as chromaffin cells and platelets. Its ability to rearrange actin filaments is important for maintaining cellular homeostasis and responsive adaptation to environmental changes.
SCIN is involved in the cytoskeletal signaling and calcium signaling pathways. It plays a role in actin filament dynamics and is related to other actin-binding proteins like gelsolin and cofilin through these pathways. SCIN interacts with phosphatidylinositol 45-bisphosphate (PIP2) and calcium ions which are important for its activity in cellular signaling networks. These pathways optimize how cells react to stimuli by altering their shape and function.
SCIN has been linked to neurodegenerative disorders and cancer. Disruptions in SCIN function can contribute to diseases such as Alzheimer’s where abnormal actin dynamics impact neuronal function. SCIN is also associated with certain cancers through its role in cell migration and metastasis. The protein may interact with tau in neurodegenerative disorders and it interacts with proteins like cortactin in cancer progression influencing cellular motility.
We have tested this species and application combination and it works. It is covered by our product promise.
We have not tested this specific species and application combination in-house, but expect it will work. It is covered by our product promise.
This species and application combination has not been tested, but we predict it will work based on strong homology. However, this combination is not covered by our product promise.
We do not recommend this combination. It is not covered by our product promise.
We are dedicated to supporting your work with high quality reagents and we are here for you every step of the way should you need us.
In the unlikely event of one of our products not working as expected, you are covered by our product promise.
Full details and terms and conditions can be found here:
Terms & Conditions.
Blocking/dilution buffer: 5% NFDM/TBST.
All lanes: Western blot - Anti-SCIN antibody [EPR16310] - C-terminal (ab199723) at 1/10000 dilution
Lane 1: Human fetal kidney lysate at 20 µg
Lane 2: HEK293 (Human embryonic kidney) whole cell lysate at 20 µg
All lanes: Anti-Rabbit IgG (HRP), specific to the non-reduced form of IgG at 1/1000 dilution
Predicted band size: 80 kDa
Observed band size: 80 kDa
Exposure time: 30s
Blocking/dilution buffer: 5% NFDM/TBST.
All lanes: Western blot - Anti-SCIN antibody [EPR16310] - C-terminal (ab199723) at 1/1000 dilution
Lane 1: Mouse kidney lysate at 10 µg
Lane 2: Mouse spleen lysate at 10 µg
Lane 3: Rat kidney lysate at 10 µg
Lane 4: Rat spleen lysate at 10 µg
All lanes: Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated at 1/1000 dilution
Predicted band size: 80 kDa
Observed band size: 80 kDa
Exposure time: 1min
Blocking/dilution buffer: 5% NFDM/TBST.
All lanes: Western blot - Anti-SCIN antibody [EPR16310] - C-terminal (ab199723) at 1/1000 dilution
Lane 1: C6 (rat glial tumor cells) whole cell lysate at 10 µg
Lane 2: PC-12 (rat adrenal gland pheochromocytoma) whole cell lysate at 10 µg
Lane 3: NIH/3T3 (mouse embryo fibroblast cells) whole cell lysate at 10 µg
All lanes: Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated at 1/1000 dilution
Predicted band size: 80 kDa
Observed band size: 80 kDa
Exposure time: 5s
Immunohistochemical analysis of paraffin-embedded Human clear cell carcinoma of kidney tissue labeling SCIN with ab199723 at 1/500 dilution followed by Goat Anti-Rabbit IgG H&L (HRP) (Goat Anti-Rabbit IgG H&L (HRP) ab97051) at 1/500 dilution. Cytoplasm staining on Human clear cell carcinoma of kidney tissue is observed. Counter stained with Hematoxylin.
Negative control: Used PBS instead of primary antibody, secondary antibody is Goat Anti-Rabbit IgG H&L (HRP) (Goat Anti-Rabbit IgG H&L (HRP) ab97051).
Perform heat mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.
Immunohistochemical analysis of paraffin-embedded Human pancreas tissue labeling SCIN with ab199723 at 1/500 dilution followed by Goat Anti-Rabbit IgG H&L (HRP) (Goat Anti-Rabbit IgG H&L (HRP) ab97051) at 1/500 dilution. Cytoplasm staining on Human pancreas tissue is observed. Counter stained with Hematoxylin.
Negative control: Used PBS instead of primary antibody, secondary antibody is Goat Anti-Rabbit IgG H&L (HRP) (Goat Anti-Rabbit IgG H&L (HRP) ab97051).
Perform heat mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
For licensing inquiries, please contact partnerships@abcam.com