MYO7A Rabbit Polyclonal Antibody

MYO7A Rabbit Polyclonal Antibody

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MYO7A Polyclonal Antibody
E91911 100ul
EUR 225
Description: Available in various conjugation types.

MYO7A Polyclonal Antibody
E-AB-92140-120uL 120uL
EUR 320
Description: Unconjugated

MYO7A Polyclonal Antibody
E-AB-92140-200uL 200uL
EUR 530
Description: Unconjugated

MYO7A Polyclonal Antibody
E-AB-92140-60uL 60uL
EUR 200
Description: Unconjugated

MYO7A Polyclonal Antibody
E-AB-92140-each each Ask for price
Description: Unconjugated

MYO7A Polyclonal Antibody
E-AB-13433-120uL 120uL
EUR 240
Description: Unconjugated

MYO7A Polyclonal Antibody
E-AB-13433-200uL 200uL
EUR 399
Description: Unconjugated

MYO7A Polyclonal Antibody
E-AB-13433-20uL 20uL
EUR 73
Description: Unconjugated

MYO7A Polyclonal Antibody
E-AB-13433-60uL 60uL
EUR 143
Description: Unconjugated

MYO7A Polyclonal Antibody
E-AB-16626-120uL 120uL
EUR 240
Description: Unconjugated

MYO7A Polyclonal Antibody
E-AB-16626-200uL 200uL
EUR 399
Description: Unconjugated

MYO7A Polyclonal Antibody
E-AB-16626-20uL 20uL
EUR 73
Description: Unconjugated

MYO7A Polyclonal Antibody
E-AB-16626-60uL 60uL
EUR 143
Description: Unconjugated

MYO7A Polyclonal Antibody
BT-AP11646-100ul 100ul Ask for price
Description: This gene is a member of the myosin gene family. Myosins are mechanochemical proteins characterized by the presence of a motor domain, an actin-binding domain, a neck domain that interacts with other proteins, and a tail domain that serves as an anchor. This gene encodes an unconventional myosin with a very short tail. Defects in this gene are associated with the mouse shaker-1 phenotype and the human Usher syndrome 1B which are characterized by deafness, reduced vestibular function, and (in human) retinal degeneration. Alternative splicing results in multiple transcript variants.

MYO7A Polyclonal Antibody
BT-AP11646-20ul 20ul Ask for price
Description: This gene is a member of the myosin gene family. Myosins are mechanochemical proteins characterized by the presence of a motor domain, an actin-binding domain, a neck domain that interacts with other proteins, and a tail domain that serves as an anchor. This gene encodes an unconventional myosin with a very short tail. Defects in this gene are associated with the mouse shaker-1 phenotype and the human Usher syndrome 1B which are characterized by deafness, reduced vestibular function, and (in human) retinal degeneration. Alternative splicing results in multiple transcript variants.

MYO7A Polyclonal Antibody
BT-AP11646-50ul 50ul Ask for price
Description: This gene is a member of the myosin gene family. Myosins are mechanochemical proteins characterized by the presence of a motor domain, an actin-binding domain, a neck domain that interacts with other proteins, and a tail domain that serves as an anchor. This gene encodes an unconventional myosin with a very short tail. Defects in this gene are associated with the mouse shaker-1 phenotype and the human Usher syndrome 1B which are characterized by deafness, reduced vestibular function, and (in human) retinal degeneration. Alternative splicing results in multiple transcript variants.

MYO7A Polyclonal Antibody
E44H08516 100ul
EUR 255
Description: Biotin-Conjugated, FITC-Conjugated , AF350 Conjugated , AF405M-Conjugated ,AF488-Conjugated, AF514-Conjugated ,AF532-Conjugated, AF555-Conjugated ,AF568-Conjugated , HRP-Conjugated, AF405S-Conjugated, AF405L-Conjugated , AF546-Conjugated, AF594-Conjugated , AF610-Conjugated, AF635-Conjugated , AF647-Conjugated , AF680-Conjugated , AF700-Conjugated , AF750-Conjugated , AF790-Conjugated , APC-Conjugated , PE-Conjugated , Cy3-Conjugated , Cy5-Conjugated , Cy5.5-Conjugated , Cy7-Conjugated Antibody

MYO7A Polyclonal Antibody
MBS9132755-002mL 0.02mL
EUR 200

MYO7A Polyclonal Antibody
MBS9132755-005mL 0.05mL
EUR 255

MYO7A Polyclonal Antibody
MBS9132755-01mL 0.1mL
EUR 345

MYO7A Polyclonal Antibody
MBS9132755-02mL 0.2mL
EUR 545

MYO7A Polyclonal Antibody
MBS9132755-5x02mL 5x0.2mL
EUR 2265

MYO7A Polyclonal Antibody
MBS8572502-01mL 0.1mL
EUR 305

MYO7A Polyclonal Antibody
MBS8572502-01mLAF405L 0.1mL(AF405L)
EUR 565

MYO7A Polyclonal Antibody
MBS8572502-01mLAF405S 0.1mL(AF405S)
EUR 565

MYO7A Polyclonal Antibody
MBS8572502-01mLAF610 0.1mL(AF610)
EUR 565

MYO7A Polyclonal Antibody
MBS8572502-01mLAF635 0.1mL(AF635)
EUR 565

MYO7A Polyclonal Antibody
MBS8530243-01mg 0.1mg
EUR 305

MYO7A Polyclonal Antibody
MBS8530243-01mLAF405L 0.1mL(AF405L)
EUR 465

MYO7A Polyclonal Antibody
MBS8530243-01mLAF405S 0.1mL(AF405S)
EUR 465

MYO7A Polyclonal Antibody
MBS8530243-01mLAF610 0.1mL(AF610)
EUR 465

MYO7A Polyclonal Antibody
MBS8530243-01mLAF635 0.1mL(AF635)
EUR 465

MYO7A Polyclonal Antibody
MBS2527365-002mL 0.02mL
EUR 135

MYO7A Polyclonal Antibody
MBS2527365-006mL 0.06mL
EUR 190

MYO7A Polyclonal Antibody
MBS2527365-012mL 0.12mL
EUR 265

MYO7A Polyclonal Antibody
MBS2527365-02mL 0.2mL
EUR 415

MYO7A Polyclonal Antibody
MBS2527365-5x02mL 5x0.2mL
EUR 1835

MYO7A Polyclonal Antibody
MBS2525891-002mL 0.02mL
EUR 135

MYO7A Polyclonal Antibody
MBS2525891-006mL 0.06mL
EUR 190

MYO7A Polyclonal Antibody
MBS2525891-012mL 0.12mL
EUR 265

MYO7A Polyclonal Antibody
MBS2525891-02mL 0.2mL
EUR 415

MYO7A Polyclonal Antibody
MBS2525891-5x02mL 5x0.2mL
EUR 1835

MYO7A Polyclonal Antibody
RD76975A-120uL 120μL
EUR 360
Description: This gene is a member of the myosin gene family. Myosins are mechanochemical proteins characterized by the presence of a motor domain, an actin-binding domain, a neck domain that interacts with other proteins, and a tail domain that serves as an anchor. This gene encodes an unconventional myosin with a very short tail. Defects in this gene are associated with the mouse shaker-1 phenotype and the human Usher syndrome 1B which are characterized by deafness, reduced vestibular function, and (in human) retinal degeneration. Alternative splicing results in multiple transcript variants.

MYO7A Polyclonal Antibody
RD76975A-200uL 200μL
EUR 630
Description: This gene is a member of the myosin gene family. Myosins are mechanochemical proteins characterized by the presence of a motor domain, an actin-binding domain, a neck domain that interacts with other proteins, and a tail domain that serves as an anchor. This gene encodes an unconventional myosin with a very short tail. Defects in this gene are associated with the mouse shaker-1 phenotype and the human Usher syndrome 1B which are characterized by deafness, reduced vestibular function, and (in human) retinal degeneration. Alternative splicing results in multiple transcript variants.

MYO7A Polyclonal Antibody
RD76975A-20uL 20μL
EUR 109.5
Description: This gene is a member of the myosin gene family. Myosins are mechanochemical proteins characterized by the presence of a motor domain, an actin-binding domain, a neck domain that interacts with other proteins, and a tail domain that serves as an anchor. This gene encodes an unconventional myosin with a very short tail. Defects in this gene are associated with the mouse shaker-1 phenotype and the human Usher syndrome 1B which are characterized by deafness, reduced vestibular function, and (in human) retinal degeneration. Alternative splicing results in multiple transcript variants.

MYO7A Polyclonal Antibody
RD76975A-60uL 60μL
EUR 214.5
Description: This gene is a member of the myosin gene family. Myosins are mechanochemical proteins characterized by the presence of a motor domain, an actin-binding domain, a neck domain that interacts with other proteins, and a tail domain that serves as an anchor. This gene encodes an unconventional myosin with a very short tail. Defects in this gene are associated with the mouse shaker-1 phenotype and the human Usher syndrome 1B which are characterized by deafness, reduced vestibular function, and (in human) retinal degeneration. Alternative splicing results in multiple transcript variants.

MYO7A Polyclonal Antibody
RD79162A-120uL 120μL
EUR 360
Description: This gene is a member of the myosin gene family. Myosins are mechanochemical proteins characterized by the presence of a motor domain, an actin-binding domain, a neck domain that interacts with other proteins, and a tail domain that serves as an anchor. This gene encodes an unconventional myosin with a very short tail. Defects in this gene are associated with the mouse shaker-1 phenotype and the human Usher syndrome 1B which are characterized by deafness, reduced vestibular function, and (in human) retinal degeneration. Alternative splicing results in multiple transcript variants.

MYO7A Polyclonal Antibody
RD79162A-200uL 200μL
EUR 630
Description: This gene is a member of the myosin gene family. Myosins are mechanochemical proteins characterized by the presence of a motor domain, an actin-binding domain, a neck domain that interacts with other proteins, and a tail domain that serves as an anchor. This gene encodes an unconventional myosin with a very short tail. Defects in this gene are associated with the mouse shaker-1 phenotype and the human Usher syndrome 1B which are characterized by deafness, reduced vestibular function, and (in human) retinal degeneration. Alternative splicing results in multiple transcript variants.

MYO7A Polyclonal Antibody
RD79162A-20uL 20μL
EUR 109.5
Description: This gene is a member of the myosin gene family. Myosins are mechanochemical proteins characterized by the presence of a motor domain, an actin-binding domain, a neck domain that interacts with other proteins, and a tail domain that serves as an anchor. This gene encodes an unconventional myosin with a very short tail. Defects in this gene are associated with the mouse shaker-1 phenotype and the human Usher syndrome 1B which are characterized by deafness, reduced vestibular function, and (in human) retinal degeneration. Alternative splicing results in multiple transcript variants.

MYO7A Polyclonal Antibody
RD79162A-60uL 60μL
EUR 214.5
Description: This gene is a member of the myosin gene family. Myosins are mechanochemical proteins characterized by the presence of a motor domain, an actin-binding domain, a neck domain that interacts with other proteins, and a tail domain that serves as an anchor. This gene encodes an unconventional myosin with a very short tail. Defects in this gene are associated with the mouse shaker-1 phenotype and the human Usher syndrome 1B which are characterized by deafness, reduced vestibular function, and (in human) retinal degeneration. Alternative splicing results in multiple transcript variants.

MYO7A Rabbit Polyclonal Antibody