FGD2 Polyclonal antibody
FGD2 Polyclonal Antibody for WB, IHC, ELISA
Host / Isotype
Rabbit / IgG
Reactivity
human
Applications
WB, IHC, ELISA
Conjugate
Unconjugated
Cat no : 27068-1-AP
Synonyms
Validation Data Gallery
Tested Applications
Positive WB detected in | Raji cells |
Positive IHC detected in | human tonsillitis tissue, human intrahepatic cholangiocarcinoma tissue Note: suggested antigen retrieval with TE buffer pH 9.0; (*) Alternatively, antigen retrieval may be performed with citrate buffer pH 6.0 |
Recommended dilution
Application | Dilution |
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Western Blot (WB) | WB : 1:500-1:2000 |
Immunohistochemistry (IHC) | IHC : 1:50-1:500 |
It is recommended that this reagent should be titrated in each testing system to obtain optimal results. | |
Sample-dependent, Check data in validation data gallery. |
Product Information
27068-1-AP targets FGD2 in WB, IHC, ELISA applications and shows reactivity with human samples.
Tested Reactivity | human |
Host / Isotype | Rabbit / IgG |
Class | Polyclonal |
Type | Antibody |
Immunogen | FGD2 fusion protein Ag25782 |
Full Name | FYVE, RhoGEF and PH domain containing 2 |
Calculated Molecular Weight | 655 aa, 75 kDa |
Observed Molecular Weight | 75 kDa |
GenBank Accession Number | BC023645 |
Gene Symbol | FGD2 |
Gene ID (NCBI) | 221472 |
RRID | AB_2880740 |
Conjugate | Unconjugated |
Form | Liquid |
Purification Method | Antigen affinity purification |
Storage Buffer | PBS with 0.02% sodium azide and 50% glycerol pH 7.3. |
Storage Conditions | Store at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage. 20ul sizes contain 0.1% BSA. |
Background Information
FGD2 is a member of the formin family of proteins, which are known for their role in regulating the assembly of actin filaments. Formins are characterized by their ability to nucleate and elongate actin filaments, and they play a crucial role in processes that require dynamic actin structures, such as cell motility and cell division. Mutations or alterations in FGD2 have been associated with certain developmental disorders and diseases. For example, mutations in FGD2 are a cause of faciogenital dysplasia (Aarskog-Scott syndrome), a condition characterized by facial and genital abnormalities and short stature.
Protocols
Product Specific Protocols | |
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WB protocol for FGD2 antibody 27068-1-AP | Download protocol |
IHC protocol for FGD2 antibody 27068-1-AP | Download protocol |
Standard Protocols | |
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Click here to view our Standard Protocols |