PROZ antibody (AbBy Fluor® 488)
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- Target See all PROZ Antibodies
- PROZ (Protein Z, Vitamin K-Dependent Plasma Glycoprotein (PROZ))
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Reactivity
- Human
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This PROZ antibody is conjugated to AbBy Fluor® 488
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Application
- Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- Cross-Reactivity
- Human
- Purification
- Purified by Protein A.
- Immunogen
- KLH conjugated synthetic peptide derived from human Protein Z
- Isotype
- IgG
- Top Product
- Discover our top product PROZ Primary Antibody
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- Application Notes
- IF(IHC-P) 1:50-200
- Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 1 μg/μL
- Buffer
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
- Preservative
- ProClin
- Precaution of Use
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
- Storage
- -20 °C
- Storage Comment
- Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
- Expiry Date
- 12 months
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- Target
- PROZ (Protein Z, Vitamin K-Dependent Plasma Glycoprotein (PROZ))
- Alternative Name
- Protein Z (PROZ Products)
- Synonyms
- PZ antibody, 1300015B06Rik antibody, betaH1 antibody, protein Z, vitamin K dependent plasma glycoprotein antibody, protein Z, vitamin K-dependent plasma glycoprotein antibody, protein Z, vitamin K-dependent plasma glycoprotein b antibody, hemoglobin Z, beta-like embryonic chain antibody, PROZ antibody, Proz antibody, prozb antibody, Hbb-bh1 antibody
- Background
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Synonyms: Protein Z, vitamin K dependent plasma glycoprotein, PROZ, PROZ_HUMAN, PZ antibody Vitamin K-dependent protein Z.
Background: This gene encodes a liver vitamin K-dependent glycoprotein that is synthesized in the liver and secreted into the plasma. The encoded protein plays a role in regulating blood coagulation by complexing with protein Z-dependent protease inhibitor to directly inhibit activated factor X at the phospholipid surface. Deficiencies in this protein are associated with an increased risk of ischemic arterial diseases and fetal loss. Mutations in this gene are the cause of protein Z deficiency. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jan 2012].
- Gene ID
- 8858
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