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Anti-IQCF6 Polyclonal Antibody

Catalog No. TMAB-07776 Copy Product Info
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Anti-IQCF6 Polyclonal Antibody is a Rabbit antibody targeting IQCF6. Anti-IQCF6 Polyclonal Antibody can be used in WB.

Anti-IQCF6 Polyclonal Antibody

Copy Product Info
🥰Excellent
Catalog No. TMAB-07776

Anti-IQCF6 Polyclonal Antibody is a Rabbit antibody targeting IQCF6. Anti-IQCF6 Polyclonal Antibody can be used in WB.

Anti-IQCF6 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-IQCF6 Polyclonal Antibody is a Rabbit antibody targeting IQCF6. Anti-IQCF6 Polyclonal Antibody can be used in WB.
Ig Type
IgG
Reactivity
Human (predicted:Mouse,Rat)
Verified Activity
Sample: A431 (Human) Cell Lysate at 30 μg
Primary: Anti-IQCF6 (TMAB-07776) at 1/1000 dilution
Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution
Predicted band size: 117 kD
Observed band size: 117 kD
Application
Recommended Dose
WB: 1:500-2000
Antibody Type
Polyclonal
Host SpeciesRabbit
Tissue SpecificityExpressed in fetal and adult testis, in germ cells but not somatic cells.
ConstructionPolyclonal Antibody
PurificationProtein A purified
AppearanceLiquid
Formulation0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
Concentration1mg/ml
Research BackgroundEncoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is about 3% of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene.
Antigen Details
Immunogen
KLH conjugated synthetic peptide: human IQCF6
Antigen Species
Human
Gene Name
IQCH
Gene ID
Protein Name
IQ domain-containing protein H
Uniprot ID
Function
May play a regulatory role in spermatogenesis.
Chemical Properties
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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