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Anti-C2orf29 Polyclonal Antibody

Catalog No. TMAB-03412 Copy Product Info
🥰Excellent
Anti-C2orf29 Polyclonal Antibody is a Rabbit antibody targeting C2orf29. Anti-C2orf29 Polyclonal Antibody can be used in WB.

Anti-C2orf29 Polyclonal Antibody

Copy Product Info
🥰Excellent
Catalog No. TMAB-03412

Anti-C2orf29 Polyclonal Antibody is a Rabbit antibody targeting C2orf29. Anti-C2orf29 Polyclonal Antibody can be used in WB.

Anti-C2orf29 Polyclonal Antibody
Pack SizePriceUSA StockGlobal StockQuantity
50 μL$2207-10 days7-10 days
100 μL$3727-10 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-C2orf29 Polyclonal Antibody is a Rabbit antibody targeting C2orf29. Anti-C2orf29 Polyclonal Antibody can be used in WB.
Ig Type
IgG
Reactivity
Human (predicted:Mouse,Rat)
Verified Activity
Sample: MCF-7 Cell (Human) Lysate at 40 μg
Primary: Anti-C2orf29 (TMAB-03412) at 1/300 dilution
Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution
Predicted band size: 55 kD
Observed band size: 55 kD
Application
Recommended Dose
WB: 1:500-2000
Antibody Type
Polyclonal
Host SpeciesRabbit
ConstructionPolyclonal Antibody
PurificationProtein A purified
AppearanceLiquid
Formulation0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
Concentration1mg/ml
Research BackgroundC2orf29, also known as C40, is a 510 amino acid protein that belongs to the UPF0760 family and is encoded by a gene that maps to human chromosome 2q11.2. As the second largest human chromosome, chromosome 2 makes up approximately 8% of the human genome and contains 237 million bases encoding over 1,400 genes. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alström syndrome, is related to mutations in the ALMS1 gene. Chromosome 2 contains a probable vestigial second centromere as well as vestigial telomeres, which gives credence to the hypothesis that human chromosome 2 formed as a result of an ancient fusion of two ancestral chromosomes, which are still present in modern day apes.
Antigen Details
Immunogen
KLH conjugated synthetic peptide: human C2orf29
Antigen Species
Human
Gene Name
CNOT11
Gene ID
Protein Name
CCR4-NOT transcription complex subunit 11
Uniprot ID
Chemical Properties
Molecular WeightTheoretical: 55 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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