HSPB1 mouse monoclonal antibody, clone OTI8C7

Name: HSPB1 mouse monoclonal antibody, clone OTI8C7
SKU: GAM924515
Price: 169 CNY
Availability: InStock

AliasesHSPB1

ReactivityHuman / Monkey

ApplicationsWB

Host / ClonalityMouse / Monoclonal

Lead timeIn stock · ships in 48h

$169/ 50μlIn stock 199 · Ready to ship

50μl$169

100μl$299

Applications & Recommended Dilution

Applications & DilutionRecommended Dilution

Recommended dilution1:500-1000

Reactivity: Human / Monkey
Assay: WB

Product Images

Product ImagesImages

HSPB1 mouse monoclonal antibody, clone OTI8C7 图 1 — Image 1 / 2HEK293T cells were transfected with the pCMV6-ENTRY control (Left lane) or pCMV6-ENTRY HSPB1 (Right lane) cDNA for 48 hrs and lysed. Equivalent amounts of cell lysates (5 ug per lane) were separated by SDS-PAGE and immunoblotted with anti-HSPB1.(1:1000)

HSPB1 mouse monoclonal antibody, clone OTI8C7 图 2 — Image 2 / 2Western blot analysis of extracts (35ug) from 3 cell lines lysates by using anti-HSPB1 monoclonal antibody. (1:500)

Product Specifications

SpecificationsProduct Specifications

Core Attributes CORE ATTRIBUTES

Species Reactivity: HumanMonkey

Applications: WB

Clone name: OTI8C7

Calculated molecular weight: 22.8 kDa

Immunogen: Full length human recombinant protein of human HSPB1 (NP_001531) produced in E.coli.

Isotype: IgG1

Host species: Mouse

Clonality: Monoclonal

Purification method: Affinity Purification

Uniprot-A: P04792

Recommended Dilution RECOMMENDED DILUTION

WB: 1:500-1000

Product Properties PRODUCT PROPERTIES

Shipping: They are shipped out with dry ice/blue ice unless customers require otherwise

Storage Condition: Store at -20°C PBS (pH 7.3) containing 1% BSA, 50% glycerol and 0.02% sodium azide.Stable for 12 months from date of receipt.

Formulation: Liquid

Storage Buffer: PBS (pH 7.3) containing 1% BSA, 50% glycerol and 0.02% sodium azide.

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].