HSP27 (HSPB1) Mouse Monoclonal Antibody [Kloon ID: LBI8D6]

The protein encoded by this gene is induced by environmental stress and developmental changes. The encoded protein is involved in stress resistance and actin organization and translocates from the cytoplasm to the nucleus upon stress induction. Defects in this gene are a cause of Charcot-Marie-Tooth disease type 2F (CMT2F) and distal hereditary motor neuropathy (dHMN) . [provided by RefSeq, Oct 2008].

Carrier-free (BSA/glycerol-free) HSPB1 mouse monoclonal antibody, clone LBI8D6

CMT2F; HEL-S-102; HMN2B; HS.76067; Hsp25; HSP27; HSP28; SRP27

Homo sapiens heat shock protein family B (small) member 1 (HSPB1), mRNA.

3315

P04792

Unconjugated

MAPK signaling pathway, VEGF signaling pathway

MAPK signaling pathway, VEGF signaling pathway

WB 1:500-1000

Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)

Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)

Stable for 1 year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and opening the cap. Aliquot will be stable at 4°C short term. For long-term storage, aliquot and store at -20°C or below. Stable for 12 months at -20°C. Avoid repeated freeze-thaw cycles.

HSPB1

https://www.ncbi.nlm.nih.gov/gene/?term=3315

https://www.uniprot.org/uniprot/P04792