The Goat Anti-Rabbit IgG(H+L) (CABS070) is a high-quality antibody developed for reliable detection and analysis of target proteins. This antibody is raised in goats and is highly reactive with rabbit IgG, making it an ideal choice for detecting and analyzing target proteins in various research settings. With a strong binding affinity to rabbit IgG, this secondary antibody allows for sensitive and specific detection of primary antibodies in Western blot experiments. Its versatility and reliability make it a valuable tool for researchers studying protein expression and localization in a wide range of biological samples.
This antibody is validated for use in WB, ELISA, CUT&Tag applications and has demonstrated reactivity against Rabbit samples.
Product Name:
Goat Anti-Rabbit IgG(H+L)
SKU:
CABS070
Size:
100μL
Reactivity:
Rabbit
Conjugate:
Unconjugated
Immunogen:
This information is considered to be commercially sensitive.
Tested Applications:
WBELISACUT&Tag
Recommended Dilution:
WB
1:1000 - 1:6000
ELISA
Recommended starting concentration is 1 μg/mL. Please optimize the concentration based on your specific assay requirements.
CUT&Tag
1:100
Positive Sample:
Rabbit control IgG
Observed MW:
25kDa(Lightchain),55kDa(Heavychain)
Secondary antibodies are affinity-purified antibodies which will work with target-specific primary antibody in the detection, sorting or purification of its specified target. Secondary antibodies offer increased versatility enabling users to use many detection systems (e.g. HRP, AP, fluorescence). They can also provide greater sensitivity through signal amplification as multiple secondary antibodies . Most commonly, secondary antibodies are generated by immunizing the host animal (different from host species of primary antibody) with a pooled population of normal immunoglobulins from the host species of primary antibody and can be further purified and modified (i.e. antibody fragmentation, label conjugation, etc.) to ensure well-characterized specificity to corresponding normal immunoglobulins.
Purification Method
Affinity purification
RRID
AB_2769651
Buffer Information
Store at -20℃. Avoid freeze / thaw cycles. Buffer: PBS containing 50% glycerol, preserved with proclin300 or sodium azide, pH 7.3.
Western blot analysis of recombinant Rabbit/Mouse/Rat control IgG Protein using Goat Anti-Rabbit IgG(H+L) (CABS070) at 1:1000 dilution. Secondary antibody: HRP Donkey Anti-Goat IgG (H+L) (CABS031) at 1:10000 dilution. Lysates/proteins: 100ng/50ng/25ng/10ng per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Basic Kit (AbGn00020). Exposure time: 3s.
CUT&Tag was performed using the CUT&Tag Assay Kit (pAG-Tn5) for Illumina (RK20265) from 10⁵ K-562 cells with 1 μg of TriMethyl-Histone H3-K4 Rabbit mAb (CAB22146), followed by incubation with Goat Anti-Rabbit IgG(H+L)(CABS070). The CUT&Tag results denote the enrichment pattern of TriMethyl-Histone H3-K4 around RPL30 gene.
