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- Table of Contents
WDR35 antibody (A07256) performs well in ELISA, IHC-P and shows reactivity with Human.
- Validated for inter-lot consistency, specificity, and reproducibility
- Committed to quality since 1993
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Immunohistochemistry of WDR35 in human testis tissue with WDR35 antibody at 5 μg/mL.
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Anti-WDR35 Antibody
WDR35 antibody
| Reactive Species | Host | Application |
|---|---|---|
| Human | Rabbit | ELISA, IHC-P |
Recommend Dilution
Application
Dilution
Species
WDR35 antibody can be used for detection of WDR35 by immunohistochemistry at 5 μg/mL.
Antibody validated: Immunohistochemistry in human samples. All other applications and species not yet tested. Optimal dilutions for each application should be determined by the researcher.
* It is recommended to optimize the amount of this reagent in each experimental system to achieve the best results.
Product Information
Product Name
Anti-WDR35 Antibody
View all WDR35 Antibodies
View all WDR35 Antibodies
Form
Liquid
Uniprot
Gene ID
Storage & Handling
WDR35 antibody can be stored at 4°C, stable for up to one year. Avoid repeated freeze-thaw cycles. Antibodies should not be exposed to prolonged high temperatures.
Host
Rabbit
Contents
WDR35 Antibody is supplied in PBS containing ≤0.09% sodium azide.
Clonality
Polyclonal
Isotype
IgG
Immunogen
WDR35 antibody was raised against a 16 amino acid synthetic peptide near the amino terminus of human WDR35. The immunogen is located within amino acids 60 - 110 of WDR35.
Cross-Reactivity
WDR35 antibody is human specific.
Observed Molecular Weight
68 kDa
Calculated Molecular Weight
133.5 kDa
Background of WDR35
WD40 repeats are a common structural module in eukaryotic proteins, and proteins containing WD40 domains have a wide range of functions, including signal transduction, cell cycle regulation, RNA splicing, and transcription. One such protein, WDR35, also known as CED2, has been shown to be mutated in patients with Sensenbrenner syndrome/cranioectodermal dysplasia (CED), an autosomal-recessive disease that is characterized by craniosynstosis and ectodermal and skeletal abnormalities. WDR35 localizes to cilia and dentrosomes during embryogenesis and human and mouse fibroblasts that lack this gene fail to produce cilia. Mutations in this gene can also cause short-rib polydactyly syndromes due to abnormal ciliogenesis.
Cite This Product
Anti-WDR35 Antibody (Boster Biological Technology, Pleasanton CA, USA, Catalog # A07256)
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Product Promise
We promise Anti-WDR35 Antibody performs excellently in relevant applications for ELISA, IHC-P. If it doesn't perform as promised, we will refund the product. Learn more
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A07256
Buy one primary antibody get one 0.5ml HRP or Biotin secondary antibody for free.
*Sample sizes are prepared on demand and will take extra lead time. (cannot be conjugated)
$481.00
Troubleshooting
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We promise all of our products perform as described in datasheets.
This product is for Research Use Only. Not for use in diagnostic procedures.
Update date:
Oct 10, 2026