OTC mouse monoclonal antibody, clone OTI2G6 (formerly 2G6)

Name: OTC mouse monoclonal antibody, clone OTI2G6 (formerly 2G6)
SKU: GAM913701
Price: 169 CNY
Availability: InStock

AliasesOrnithine Carbamoyltransferase

ReactivityHuman / Mouse / Rat

ApplicationsIHC · WB

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

IHC

Recommended dilutionNo data

Reactivity: Human / Mouse / Rat
Assay: IHC

Recommended dilution1:2000

Reactivity: Human / Mouse / Rat
Assay: WB

Product Images

Product ImagesImages

OTC mouse monoclonal antibody, clone OTI2G6 (formerly 2G6) 图 1 — Image 1 / 2No text caption for this image

OTC mouse monoclonal antibody, clone OTI2G6 (formerly 2G6) 图 2 — Image 2 / 2Immunohistochemical staining of paraffin-embedded Human liver tissue within the normal limits using anti-OTC mouse monoclonal antibody. (GAM913701) Dilution: 1:150. Heat-induced epitope retrieval by EDTA solution buffer pH 8.0 at 120°C for 3 min.

Product Specifications

SpecificationsProduct Specifications

Core Attributes CORE ATTRIBUTES

Species Reactivity: HumanMouseRat

Applications: IHCWB

Clone name: OTI2G6

Calculated molecular weight: 36.1 kDa

Immunogen: Human recombinant protein fragment corresponding to amino acids 33-354 of human OTC (NP_000522)produced in SF9 cell.

Isotype: IgG2a

Host species: Mouse

Clonality: Monoclonal

Purification method: Affinity Purification

Uniprot-A: P00480

Recommended Dilution RECOMMENDED DILUTION

WB: 1:2000

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.

This nuclear gene encodes a mitochondrial matrix enzyme. Missense, nonsense, and frameshift mutations in this enzyme lead to ornithine transcarbamylase deficiency, which causes hyperammonemia. Since the gene for this enzyme maps close to that for Duchenne muscular dystrophy, it may play a role in that disease also. [provided by RefSeq, Jul 2008]