Primary indication for advanced muscle wasting therapies and research
Origin of Medicine
Biotechnological synthesis
Salt Composition
Recombinant GDF-8 analogue
Drug Type
Biological injectable
Ingredients
Recombinant Myostatin (GDF-8) analogues, sterile water for injection, stabilizing agents
Physical Form
Liquid
Function
Promotes muscle hypertrophy by inhibiting myostatin activity
Recommended For
Muscle growth, performance enhancement, research purposes
Dosage
1 mg per vial (as per vial marking)
Dosage Guidelines
As directed by healthcare professional or researcher
Suitable For
Adults
Quantity
1 vial per box
Storage Instructions
Store in a cool, dry place at 2-8C; protect from light
Caution
For research use or prescribed professional administration only; not for self-administration
Molecular Weight
Approx. 26 kDa (GDF-8 protein)
Route of Administration
Intramuscular or subcutaneous injection
Registration Status
Not for retail sale, laboratory/clinical research use only
Appearance
Clear to light yellow liquid
Shelf Life
24 months from manufacturing date (when stored as instructed)
Sterility
Sterile, single-use vial
GDF-8 Injection gold bond Trade Information
Supply Ability
100 Per Day
Delivery Time
7 Days
Sample Available
No
Sample Policy
Contact us for information regarding our sample policy
About GDF-8 Injection gold bond
Strength
2mg-10mg
Age Group
Adult
Purity
100%
Grade
A1
Usage/Application
Muscle Building
Brand
GOLD BOND LABS
Dose
1 mg
Packaging Size
1mg X 3 Vials
Quantity Per Pack
1mg X 3 Vials
Minimum Order Quantity
5 Pack
Product Specification
Usage
Recombinant Myostatin
Packaging Size
3 Vials
Dose
1mg X 3 Vials
Packaging Type
Box
Product Description
Our firm is a foremost name, involved in providing a diverse range ofiRecombinant Myostatin GDF-8 Injection.iExperts use the advanced techniques to develop this product as per client's demand.
Precise Muscle Growth Enhancement
GDF-8 Injection Gold Bond works by inhibiting myostatin activity, which in turn promotes muscle hypertrophy. This action makes it valuable for research into muscle wasting therapies and performance enhancement studies. The standardized 1 mg dosage per vial allows for consistent experimental results, provided the administration is conducted by qualified professionals.
Safe and Controlled Application
Each sterile vial is intended for single use and should be administered either intramuscularly or subcutaneously, as directed by a healthcare professional or qualified researcher. Laboratory or clinical settings are recommended for its use, ensuring adherence to safety protocols and regulatory guidelines. The formulation remains stable for up to 24 months when stored correctly.
FAQ's of GDF-8 Injection gold bond:
Q: How should GDF-8 Injection Gold Bond be stored for maximum shelf life?
A: Store the injection in a cool, dry place at temperatures between 2-8C, ensuring it is protected from light. Proper storage conditions help maintain sterility and effectiveness for up to 24 months from the manufacturing date.
Q: What is the recommended route of administration for this injection?
A: GDF-8 Injection Gold Bond is designed for intramuscular or subcutaneous injection, and should be administered by a qualified healthcare professional or researcher in a controlled setting.
Q: Can individuals self-administer this product for muscle growth?
A: No, self-administration is not recommended. This product is intended only for research use or prescribed professional administration, and should not be used without appropriate supervision.
Q: Who is suitable to receive GDF-8 Injection Gold Bond?
A: The product is suitable for adults participating in approved research studies or advanced therapeutic protocols for muscle wasting. It is not available for retail or general consumer use.
Q: What are the key benefits of using GDF-8 Injection Gold Bond in research applications?
A: The primary benefit is its ability to promote muscle hypertrophy via myostatin inhibition, making it valuable for studying muscle growth, performance enhancement, and muscle wasting conditions.
Q: Where should the injection be performed to ensure safety and compliance?
A: Administration should take place in laboratory or clinical environments under professional supervision, strictly adhering to institutional safety guidelines and regulatory requirements.
Q: What process should be followed for dosage and administration?
A: Use the 1 mg (per vial) dosage as marked, following specific instructions provided by a healthcare professional or designated researcher. Exact dosage may vary depending on the research protocol or treatment plan.
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