ARG65296
anti-MYO5A antibody
anti-MYO5A antibody for ICC/IF,Western blot and Human,Mouse
Metabolism antibody; Neuroscience antibody; Signaling Transduction antibody
Overview
Product Description | Goat Polyclonal antibody recognizes MYO5A |
---|---|
Tested Reactivity | Hu, Ms |
Predict Reactivity | Cow, Rat |
Tested Application | ICC/IF, WB |
Specificity | This antibody is expected to recognize both reported isoforms (NP_000250.3; NP_001135967.1). |
Host | Goat |
Clonality | Polyclonal |
Isotype | IgG |
Target Name | MYO5A |
Antigen Species | Human |
Immunogen | C-ETKQLELDLN |
Conjugation | Un-conjugated |
Alternate Names | GS1; MYH12; Unconventional myosin-Va; MYR12; Myosin-12; MYO5; Dilute myosin heavy chain, non-muscle; Myoxin; Myosin heavy chain 12 |
Application Instructions
Application Suggestion |
|
||||||
---|---|---|---|---|---|---|---|
Application Note | WB: Recommend incubate at RT for 1h. * The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist. |
Properties
Form | Liquid |
---|---|
Purification | Purified from goat serum by antigen affinity chromatography. |
Buffer | Tris saline (pH 7.3), 0.02% Sodium azide and 0.5% BSA. |
Preservative | 0.02% Sodium azide |
Stabilizer | 0.5% BSA |
Concentration | 0.5 mg/ml |
Storage Instruction | For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C or below. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use. |
Note | For laboratory research only, not for drug, diagnostic or other use. |
Bioinformation
Database Links | |
---|---|
Background | This gene is one of three myosin V heavy-chain genes, belonging to the myosin gene superfamily. Myosin V is a class of actin-based motor proteins involved in cytoplasmic vesicle transport and anchorage, spindle-pole alignment and mRNA translocation. The protein encoded by this gene is abundant in melanocytes and nerve cells. Mutations in this gene cause Griscelli syndrome type-1 (GS1), Griscelli syndrome type-3 (GS3) and neuroectodermal melanolysosomal disease, or Elejalde disease. Multiple alternatively spliced transcript variants encoding different isoforms have been reported, but the full-length nature of some variants has not been determined. [provided by RefSeq, Dec 2008] |
Research Area | Metabolism antibody; Neuroscience antibody; Signaling Transduction antibody |
Calculated MW | 215 kDa |