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Mouse Anti-MRAS Recombinant Antibody (CBFYM-2528) (CBMAB-M2715-FY)

This product is mouse antibody that recognizes MRAS. The antibody CBFYM-2528 can be used for immunoassay techniques such as: WB, FC, IF.
See all MRAS antibodies
Published Data

Summary

Host Animal
Mouse
Specificity
Human
Clone
CBFYM-2528
Antibody Isotype
IgG2a
Application
WB, FC, IF

Basic Information

Immunogen
Full length human recombinant protein of human MRAS (NP_036351) produced in HEK293T cell
Specificity
Human
Antibody Isotype
IgG2a
Clonality
Monoclonal
Application Notes
The COA includes recommended starting dilutions, optimal dilutions should be determined by the end user.

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

Format
Liquid
Storage
Store at +4°C short term (1-2 weeks). Aliquot and store at -20°C long term. Avoid repeated freeze/thaw cycles.

Target

Full Name
MUSCLE RAS ONCOGENE HOMOLOG
Introduction
This gene encodes a member of the Ras family of small GTPases. These membrane-associated proteins function as signal transducers in multiple processes including cell growth and differentiation, and dysregulation of Ras signaling has been associated with many types of cancer. The encoded protein may play a role in the tumor necrosis factor-alpha and MAP kinase signaling pathways. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene.
Entrez Gene ID
UniProt ID
Alternative Names
Muscle RAS Oncogene Homolog; Ras-Related Protein R-Ras3; RRAS3; Muscle And Microspikes RAS; Ras-Related Protein M-Ras; R-RAS3; M-RAs
Function
Serves as an important signal transducer for a novel upstream stimuli in controlling cell proliferation. Activates the MAP kinase pathway.
Biological Process
Actin cytoskeleton organization Source: ProtInc
Cellular response to leukemia inhibitory factor Source: Ensembl
Ras protein signal transduction Source: UniProtKB
Cellular Location
Cell membrane
Involvement in disease
Noonan syndrome 11 (NS11):
A form of Noonan syndrome, a disease characterized by short stature, facial dysmorphic features such as hypertelorism, a downward eyeslant and low-set posteriorly rotated ears, and a high incidence of congenital heart defects and hypertrophic cardiomyopathy. Other features can include a short neck with webbing or redundancy of skin, deafness, motor delay, variable intellectual deficits, multiple skeletal defects, cryptorchidism, and bleeding diathesis. Individuals with Noonan syndrome are at risk of juvenile myelomonocytic leukemia, a myeloproliferative disorder characterized by excessive production of myelomonocytic cells. NS11 inheritance is autosomal dominant.
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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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