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. 2020 Oct 14;16:1744806920963807. doi: 10.1177/1744806920963807

Table 1.

Primary antibodies and IgG controls used in this study.

Antibody Host Supplier/Cat#/RRIDb Dilution
IB4 LF/I21413 1.0 µg/ml
CaV3.2a Rabbit polyclonal Alomone/ACC025/AB2039781 1:500 (IHC), 1:1000 (Wb)
ATF3 Rabbit polyclonal SCB/SC188 1:200 (IHC), 1:800 (Wb)
Iba1 Rabbit polyclonal Wako/019-19741 1:1000 (IHC)
GFAP Rabbit polyclonal monoclonal Dako/Z0334 1:500 (IHC)
Tubb3 Mouse monoclonal monoclonal SCB/sc-80016 1:400 (IHC), 1:1000 (Wb)
GAPDH Mouse monoclonal monoclonal Sigma/SAB1403850 1:2000 (WB)
IgG control Mouse LF/31903 1:100∼400
IgG control Rabbit LF/MA5-16384 1:100∼1000

CaV3.2: T-type voltage-gated calcium channel 3.2; IB4: isolectin IB4; ATF3: activated transcriptional factor 3; Iba1: ionized calcium-binding adapter molecule 1; GFAP: glial fibrillary acidic protein; Tubb3: β3-Tubulin; GAPDH: glycolytic enzyme glyceraldehyde-3-phosphate dehydrogenase; IgG: immunoglobulin G; IHC: immunohistochemistry; WB: weight bearing.

aAntigenic peptide: CHVEGPQERARVAHS, corresponding to amino acid residues 581–595 of rat CaV3.2 intracellular loop between domains D1 and D2.

bLF, Life Technologies, Carlsbad, CA; Alomone, Alomone Labs, Jerusalem, Israel; SCB, Santa Cruz Biotechnology, Santa Cruz, CA; Wako, Richmond, VA; Dako: Carpinteria, California; Sigma, Sigma–Aldrich, St Louis, MO.