HRP-conjugated Goat Anti-Rat IgG(H+L)

Cat No. SA00001-15

Applications

ELISA, WB, Dot blot

Conjugate

HRP

Host

Goat

Reactivity

Rat

Size: 

-/ -

Freight/Packing: -

Quantity

Please visit your regions distributor:


Product Information

Concentration 0.2 mg/mL
Applications ELISA, WB, Dot blot
Host Species Goat
Species Reactivity Rat
Physical State Liquid
Suggested Dilution Range 1:1000-1:5000 for western blotting with ECL substrates
1:1000-1:20,000 for ELISA and Western blotting with chromogenic substrates
Purity The antibody was purified from antisera by immunoaffinity chromatography using antigens coupled to agarose beads.
Storage Buffer 0.01 M Sodium phosphate, 0.25 M NaCl, 50% glycerol, 3 mg/ml BSA, pH 7.6.
Storage Instructions Store at -20°C. Stable for one year after shipment.
Stabilizer3 mg/ml BSA
ClonalityPolyclonal
RRIDAB_2864369
NoteThis product is for research use only,not for diagnostic or therapeutic use.

Publications

Title

Cell Metab

Dual impacts of serine/glycine-free diet in enhancing antitumor immunity and promoting evasion via PD-L1 lactylation

Authors - Huan Tong

Adv Sci (Weinh)

cAMP-Induced Nuclear Condensation of CRTC2 Promotes Transcription Elongation and Cystogenesis in Autosomal Dominant Polycystic Kidney Disease.

Authors - Zeyun Mi

Nat Commun

TBC1D23 mediates Golgi-specific LKB1 signaling

Authors - Yingfeng Tu

J Pineal Res

Melatonin pretreatment alleviates the long-term synaptic toxicity and dysmyelination induced by neonatal Sevoflurane exposure via MT1 receptor-mediated Wnt signaling modulation.

Authors - Lirong Liang

Nat Commun

Chimeric design of pyrrolysyl-tRNA synthetase/tRNA pairs and canonical synthetase/tRNA pairs for genetic code expansion.

Authors - Wenlong Ding

J Clin Invest

Iron-dependent epigenetic modulation promotes pathogenic T cell differentiation in lupus.

Authors - Xiaofei Gao

Reviews

The reviews below have been submitted by verified Proteintech customers who received an incentive for providing their feedback.


FH

Danielle (Verified Customer) (09-11-2025)

We observed signal in tissues that we expected to be positive in our testing of Ly6G primary antibody on various mouse immune tissues. We also had a very clean negative secondary-only control. For our testing, we used a 1:1000 dilution for the secondary and used Tris-EDTA antigen retrieval for the experiment. In future studies, we will likely need to use 1:750 for better signal intensity.

  • Applications: Immunohistochemistry
  • Primary Antibody Dilution: Secondary Antibody: 1:1000
  • Cell Tissue Type: Mouse bone marrow, mouse lung, mouse plasmacytoma
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