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Anti-C16orf7 Polyclonal Antibody

Catalog No. TMAB-03306 Copy Product Info
🥰Excellent
Anti-C16orf7 Polyclonal Antibody is a Rabbit antibody targeting C16orf7. Anti-C16orf7 Polyclonal Antibody can be used in WB.

Anti-C16orf7 Polyclonal Antibody

Copy Product Info
🥰Excellent
Catalog No. TMAB-03306

Anti-C16orf7 Polyclonal Antibody is a Rabbit antibody targeting C16orf7. Anti-C16orf7 Polyclonal Antibody can be used in WB.

Anti-C16orf7 Polyclonal Antibody
Pack SizePriceUSA StockGlobal StockQuantity
50 μL$2227-10 days7-10 days
100 μL$3737-10 days7-10 days
200 μL$5277-10 days7-10 days
For In stock only · Estimated delivery: USA Stock (1-2 days) Global Stock (5-7 days)
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For research use only—not for human use. No sales to individuals. Use as intended only.
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Product Introduction

Bioactivity
Description
Anti-C16orf7 Polyclonal Antibody is a Rabbit antibody targeting C16orf7. Anti-C16orf7 Polyclonal Antibody can be used in WB.
Ig Type
IgG
Reactivity
Human,Rat (predicted:Mouse,Cow)
Verified Activity
Sample:
SY5Y (Human) Cell Lysate at 30 μg
Primary: Anti-C16orf7 (TMAB-03306) at 1/1000 dilution
Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution
Predicted band size: 69 kD
Observed band size: 69 kD
Application
Recommended Dose
WB: 1:500-2000
Antibody Type
Polyclonal
Host SpeciesRabbit
Subcellular LocalizationUbiquitous.
ConstructionPolyclonal Antibody
PurificationProtein A purified
AppearanceLiquid
Formulation0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
Concentration1mg/ml
Research BackgroundChromosome 16 encodes over 900 genes in approximately 90 million base pairs, makes up nearly 3% of human cellular DNA and is associated with a variety of genetic disorders. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, though through the CREBBP gene which encodes a critical CREB binding protein. Signs of Rubinstein-Taybi include mental retardation and predisposition to tumor growth and white blood cell neoplasias. Crohn's disease is a gastrointestinal inflammatory condition associated with chromosome 16 through the NOD2 gene. An association with systemic lupus erythematosis and a number of other autoimmune disorders with the pericentromeric region of chromosome 16 has led to the identification of SLC5A11 as a potential autoimmune modifier.
Antigen Details
Immunogen
KLH conjugated synthetic peptide: human C16orf7/ATP-BL
Antigen Species
Human
Gene Name
VPS9D1
Gene ID
Protein Name
VPS9 domain-containing protein 1
Uniprot ID
Chemical Properties
Molecular WeightTheoretical: 69 kDa.
Stability & Storage
Stability & StorageStore at 2°C-8°C for 1 month. Store at -20°C or -80°C for 12 months. Avoid repeated freeze-thaw cycles.
TransportShipping with blue ice.

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