Mouse Anti-SERPINC1 Recombinant Antibody (clone 22B11)

CAT#: MOB-1168z

This product is a mouse antibody that recognizes human SERPINC1. It can be used in the following applications: ELISA, WB, FuncS.

Gene Expression
Figure 1 Liver Figure 2 RNA cell line category: Cell line enriched (Hep G2)

Specifications

  • Immunogen
  • Human Serpin Peptidase Inhibitor, Clade C (Antithrombin), Member 1
  • Host Species
  • Mouse
  • Derivation
  • Mouse
  • Type
  • Mouse IgG1
  • Specificity
  • Human SERPINC1
  • Species Reactivity
  • Human
  • Clone
  • 22B11
  • Applications
  • ELISA, WB, FuncS

Product Property

  • Purity
  • >95% as determined by SDS-PAGE
  • Concentration
  • Please refer to the vial label for the specific concentration.
  • Storage
  • Store at 4°C short term (1-2 weeks). Aliquot and store at -20°C long term. Avoid repeated freeze/thaw cycles.

Applications

  • Application Notes
  • This antibody has been reported for use in Enzyme-linked Immunosorbent Assay, Western blot, Functional Study.

Target

  • Alternative Names
  • SERPINC1; AT3D; Signal Peptide Antithrombin Part 1; Antithrombin III; AT3; Antithrombin-III; THPH7; Serpin C1; Antithrombin (Aa 375-432); Serine (Or Cysteine) Proteinase Inhibitor, Clade C (Antithrombin), Member 1; Coding Sequence Signal Peptide Antithrom
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Product Notes

This is a product of Creative Biolabs' Hi-Affi™ recombinant antibody portfolio, which has several benefits including:

• Increased sensitivity
• Confirmed specificity
• High repeatability
• Excellent batch-to-batch consistency
• Sustainable supply
• Animal-free production

See more details about Hi-Affi™ recombinant antibody benefits.

Datasheet

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COA

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CAT Product Name Application Type
NEUT-1943CQ Recombinant Mouse Anti-SERPINC1 Antibody (BDI205) WB, BL, ELISA, Dot, ICC, IF, IHC-P, IP IgG1
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For research use only. Not intended for any clinical use. No products from Creative Biolabs may be resold, modified for resale or used to manufacture commercial products without prior written approval from Creative Biolabs.

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