Anti-MYL3 Antibody

$99.00$319.00

Reactivity: Human,Mouse,Rat
Applications: ELISA,WB,IHC
Conjugation: Various
Supplier: CUSABIO BIOTECH CO.

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Rabbit Anti-MYL3 Antibody (CSB-PA015310DSR2HU)

Supplier: CUSABIO BIOTECH CO.

Alternative names:

Myosin light chain 3Curated Antibody,Cardiac myosin light chain 1 Antibody,MYL3 Antibody

More alternative names for the antibody
Cardiac myosin light chain 1 antibody|CMH8 antibody|CMLC1 antibody|MLC1SB antibody|MLC1V antibody|MYL3 antibody|MYL3_HUMAN antibody|Myosin light chain 1 antibody|Myosin light chain 1 slow twitch muscle B ventricular isoform antibody|myosin light chain 3 alkali ventricular skeletal slow antibody|Myosin light chain 3 antibody|slow-twitch muscle B/ventricular isoform antibody|Ventricular slow twitch myosin alkali light chain antibody|Ventricular/slow twitch myosin alkali light chain antibody|VLC1 antibody
Anti-Myosin light chain 3 antibody [MLM527] (ab680)
Close sc-365243|sc-98928|sc-100342|sc-168680|sc-376606|sc-9449|

Recommended applications: ELISA, WB, IHC

Recommended dilution: User optimized

Recommended protocols: check protocols

Name

Anti-MYL3 Antibody

Catalogue No.

CSB-PA015310DSR2HU

Reactivity

Human, Mouse, Rat

Immunogen

Recombinant human Myosin light chain 3 protein (1-195AA)

Host

Rabbit

Applications

ELISA, WB, IHC

Recommended dilution

User optimized

Clonality

Polyclonal

Conjugation

unconjugated

Isotype

IgG

Molecular weight

21 kDa

Purification

Antigen Affinity Purified

Storage

Shipped at 4 Celcius Degree. Upon delivery aliquot and store at -20 Celcius Degree or -80 Celcius Degree. Avoid repeated freeze.

Database links

Entrez Gene:618352( Cow), Entrez Gene:4634( Human), Entrez Gene:17897( Mouse), Entrez Gene:24585( Rat), Omim:160790( Human), SwissProt:P85100( Cow), SwissProt:P08590( Human), SwissProt:P09542( Mouse), SwissProt:P16409( Rat), Unigene:517939( Human), Unigene:7353( Mouse), Unigene:1955( Rat)

Protein function

Regulatory light chain of myosin. Does not bind calcium.

Involvement in disease

Cardiomyopathy, familial hypertrophic 8 (CMH8) [MIM:608751]: A hereditary heart disorder characterized by ventricular hypertrophy, which is usually asymmetric and often involves the interventricular septum. The symptoms include dyspnea, syncope, collapse, palpitations, and chest pain. They can be readily provoked by exercise. The disorder has inter- and intrafamilial variability ranging from benign to malignant forms with high risk of cardiac failure and sudden cardiac death. Rarely, patients present a variant of familial hypertrophic cardiomyopathy, characterized by mid-left ventricular chamber thickening. . Note=The disease is caused by mutations affecting the gene represented in this entry.

Protein post-translational modifications

The N-terminus is blocked.; N-terminus is methylated by METTL11A/NTM1. .

Research area

All research areas>Structural Proteins>Myosin
(View all antibody categories related to Structural Proteins)

Note

AntibodyPlus provides antibody trial sample for your own antibody validation and collects antibody reviews.

Supplier

CUSABIO BIOTECH CO.

Product type

Primary antibody

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