PRKCD/PRKCQ/Prkcd Recombinant Monoclonal Antibody

Code CSB-RA057607A0HU
Size US$210
Order now
Image
  • Western Blot
    Positive WB detected in: THP-1 whole cell lysate(30µg), A431 whole cell lysate(30µg), Jurkat whole cell lysate(30µg), HT-29 whole cell lysate(30µg), MCF7 whole cell lysate(30µg), A375 whole cell lysate(30µg), Mouse brain tissue lysate(30µg), Rat brain tissue lysate(30µg)
    All lanes: PKC delta/theta antibody at 1:1000
    Secondary
    Goat polyclonal to rabbit IgG at 1/40000 dilution
    Predicted band size: 78 kDa
    Observed band size: 78 kDa
    Exposure time:2min
  • IHC image of CSB-RA057607A0HU diluted at 1:100 and staining in paraffin-embedded human lung tissue performed on a Leica BondTM system. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4°C overnight. The primary is detected by a Goat anti-rabbit polymer IgG labeled by HRP and visualized using 0.05% DAB.
  • IHC image of CSB-RA057607A0HU diluted at 1:100 and staining in paraffin-embedded human liver cancer performed on a Leica BondTM system. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4°C overnight. The primary is detected by a Goat anti-rabbit polymer IgG labeled by HRP and visualized using 0.05% DAB.
  • Immunofluorescence staining of HeLa cell with CSB-RA057607A0HU at 1:50 , counter-stained with DAPI. The cells were fixed in 4% formaldehyde, permeabilized using 0.2% Triton X-100 and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4°C. The secondary antibody was Alexa Fluor 488-congugated AffiniPure Goat Anti-Rabbit IgG(H+L).
  • Overlay Peak curve showing A431 cells stained with CSB-RA057607A0HU (red line) at 1:100. The cells were fixed in 4% formaldehyde and permeated by 0.2% TritonX-100 for 10min. Then 10% normal goat serum to block non-specific protein-protein interactions followed by the antibody (1ug/1*106cells) for 45min at 4℃. The secondary antibody used was FITC-conjugated goat anti-rabbit IgG (H+L) at 1/200 dilution for 35min at 4℃.Control antibody (green line) was Rabbit IgG (1ug/1*106cells) used under the same conditions. Acquisition of >10, 000 events was performed.
Have Questions? Leave a Message or Start an on-line Chat

Product Details

Uniprot No.
Target Names
PRKCD/PRKCQ/Prkcd
Alternative Names
CVID9 antibody; D14Ertd420e antibody; Kinase PKC delta antibody; KPCD antibody; KPCD_HUMAN antibody; MAY 1 antibody; MAY1 antibody; MGC49908 antibody; nPKC delta antibody; nPKC-delta antibody; PCKd antibody; PKC d antibody; PKC delta antibody; PKCD antibody; PKCdelta antibody; PRKC D antibody; PRKC delta antibody; Prkcd antibody; Protein Kinase C delta antibody; Protein kinase C delta type antibody; Protein kinase C delta VIII antibody; Protein Kinase Cdelta antibody; Tyrosine protein kinase PRKCD antibody; KPCT_HUMAN antibody; MGC126514 antibody; MGC141919 antibody; nPKC theta antibody; nPKC-theta antibody; nPKCtheta antibody; OTTHUMP00000043364 antibody; OTTHUMP00000043365 antibody; PKC 0 antibody; PKC0 antibody; Prkcq antibody; PRKCT antibody; Protein kinase C theta antibody; Protein kinase C theta type antibody; Protein Kinase Ctheta antibody;Prkcd; PkcdProtein kinase C delta type; EC 2.7.11.13; Tyrosine-protein kinase PRKCD; EC 2.7.10.2; nPKC-delta) [Cleaved into: Protein kinase C delta type regulatory subunit; Protein kinase C delta type catalytic subunit; Sphingosine-dependent protein kinase-1; SDK1)]
Species Reactivity
Human, Mouse, Rat
Immunogen
A synthesized peptide from human PRKCD/PRKCQ/Prkcd protein
Immunogen Species
Homo sapiens (Human)
Conjugate
Non-conjugated
Clonality
Monoclonal
Isotype
Rabbit IgG
Clone No.
24F7
Purification Method
Affinity-chromatography
Concentration
It differs from different batches. Please contact us to confirm it.
Buffer
Rabbit IgG in 10mM phosphate buffered saline , pH 7.4, 150mM sodium chloride, 0.05% BSA, 0.02% sodium azide and 50% glycerol.
Form
Liquid
Tested Applications
ELISA, WB, IHC, IF, FC
Recommended Dilution
Application Recommended Dilution
WB 1:500-1:5000
IHC 1:50-1:200
IF 1:50-1:200
FC 1:50-1:200
Troubleshooting and FAQs
Storage
Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
Lead Time
Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.
Description

Protein kinase C delta and theta isoforms represent critical nodes in cellular signaling networks, mediating diverse processes including apoptosis, immune cell activation, and proliferation. PKC delta functions as a tumor suppressor in many contexts and plays essential roles in oxidative stress responses, while PKC theta is particularly important in T cell receptor signaling and immune function. The involvement of these kinases in cancer biology, inflammation, and metabolic regulation makes them valuable targets for researchers investigating fundamental cell biology and disease mechanisms.

This recombinant monoclonal antibody, produced from a stable rabbit host and defined by clone 24F7, offers the reproducibility that demanding experimental workflows require. Because recombinant production ensures sequence-defined consistency between lots, researchers can confidently compare results across extended studies without concerns about batch-to-batch variation that can complicate data interpretation with traditional hybridoma-derived antibodies.

Validation across multiple platforms demonstrates genuine experimental flexibility. Western blot analysis confirms detection at the expected 78 kDa molecular weight across diverse human cell lines including THP-1, A431, Jurkat, HT-29, MCF7, and A375, with cross-species reactivity confirmed in mouse and rat brain tissue lysates. Immunohistochemistry staining has been validated in human lung tissue and liver cancer sections using citrate buffer antigen retrieval, while immunofluorescence studies in HeLa cells reveal clear cytoplasmic localization patterns. Flow cytometry applications have been demonstrated in A431 cells with distinct signal separation from isotype controls.

The broad application compatibility and validated cross-species reactivity make this antibody particularly suitable for comparative studies examining PKC delta and theta signaling in oncology research, immunology, and neuroscience applications where consistent, reliable detection is essential.

Usage
For Research Use Only. Not for use in diagnostic or therapeutic procedures.

Customer Reviews and Q&A

 Customer Reviews

There are currently no reviews for this product.

Submit a Review here

icon of phone
Call us
301-363-4651 (Available 9 a.m. to 5 p.m. CST from Monday to Friday)
icon of address
Address
No. 269, Shendun 5th Road, Donghu Hi-Tech Development Area, Hubei Province, 430206, P.R.China
icon of social media
Join us with

Subscribe newsletter

Leave a message

* To protect against spam, please pass the CAPTCHA test below.
CAPTCHA verification
© 2007-2026 CUSABIO TECHNOLOGY LLC All rights reserved. 鄂ICP备15011166号-1
Place an order now

I. Product details

*
*
*
*

II. Contact details

*
*

III. Ship To

*
*
*
*
*
*
*

IV. Bill To

*
*
*
*
*
*
*
*