Recombinant Zebrafish ACTA1B

• Cat.No.: ACTA1B-12799Z
• Product Overview: Recombinant Zebrafish ACTA1B full length or partial length protein was expressed.

Specification

• Source: Mammalian Cells
• Species: Zebrafish
• Tag: His
• Form: Liquid or lyophilized powder
• Endotoxin: < 1.0 eu per μg of the protein as determined by the LAL method.
• Purity: >80%
• Notes: This item requires custom production and lead time is between 5-9 weeks. We can custom produce according to your specifications.
• Storage: Store it at +4 oC for short term. For long term storage, store it at -20 oC～-80 oC.
• Storage Buffer: PBS buffer

Gene Information

• Gene Name: acta1b actin, alpha 1b, skeletal muscle [ Danio rerio (zebrafish) ]
• Official Symbol: ACTA1B
• Gene ID: 407658
• mRNA Refseq: NM_214784
• Protein Refseq: NP_999949
• UniProt ID: Q4KMI7

Reviews

08/16/2022

The company's commitment to quality assurance is evident in the protein product

03/21/2022

Its purity and consistency have exceeded my expectations

01/19/2021

The protein product's packaging and labeling were excellent

06/14/2018

It has proven to be highly soluble and easy to work wit

01/22/2016

Its high bioactivity and stability have allowed me to achieve accurate and meaningful data

Q&As

What is the role of Actin alpha 1 skeletal muscle b in muscle function?

Actin alpha 1 skeletal muscle b is a major component of the contractile apparatus in skeletal muscle, playing a crucial role in muscle contraction.

How does the expression pattern of Acta1b differ from Acta1a during early muscle development in zebrafish?

The expression pattern of Acta1b during early muscle development in zebrafish is similar to Acta1a. Both genes are expressed and play a role in muscle development during this stage.

What is the specific role of Acta1b in zebrafish?

The specific role of Acta1b in zebrafish is related to skeletal muscle development, similar to Acta1a. It contributes to the formation and function of skeletal muscle fibers.

Is Actin alpha 1 skeletal muscle b specific to skeletal muscle tissue?

Yes, Actin alpha 1 skeletal muscle b is predominantly expressed in skeletal muscle tissue and is a specialized isoform of actin found in those muscles.

which species is ACTA1B present?

It is prensent in zebrafish.

How does Actin alpha 1 skeletal muscle b contribute to muscle contraction?

 Actin alpha 1 skeletal muscle b combines with other proteins, such as myosin, to form actin filaments that interact with myosin filaments. This interaction generates the force necessary for muscle contraction.

Are there any notable structural or functional differences between Acta1a and Acta1b in zebrafish?

Acta1a and Acta1b in zebrafish have a high degree of structural similarity. They share common features and functions as skeletal muscle α-actin isoforms.

What is the full name of ACTA1B protein?

Actin alpha 1 skeletal muscle b (acta1b) plays a role upstream or down- stream of embryonic cardiac tube development and skeletal muscle fiber development and is expressed in the cardiovascular system and myoblasts

Can alterations in Actin alpha 1 skeletal muscle b affect muscle function?

Yes, mutations or disruptions in Actin alpha 1 skeletal muscle b can lead to muscle dysfunction and contribute to the development of muscle disorders, such as nemaline myopathy.

What immunogen of ACTA1B protein?

Its immunogen is recombinant zebrafish actin protein.

Which function is ACTA1B related to?

ACTA1B is closely related to the function of skeletal muscle.

Are there any specific research or therapeutic implications associated with Actin alpha 1 skeletal muscle b?

Understanding the structure and function of Actin alpha 1 skeletal muscle b, as well as its role in muscle disorders, can contribute to research efforts aimed at developing potential therapies for muscle-related conditions.

Are there any mutations or genetic variations associated with Actin alpha 1 skeletal muscle b?

Yes, mutations in the Actin alpha 1 skeletal muscle b gene (ACTA1) can lead to various muscle disorders, including nemaline myopathy, a condition characterized by muscle weakness and the presence of nemaline bodies in muscle fibers.