89-933-722

CASP1 Mouse anti-Human, Clone: 14F468, Abnova™

Manufacturer: Abnova Corporation

Select a Size

Pack Size SKU Availability Price
Each of 1 89-933-722-Each-of-1 In Stock ₹ 85,173.00

89-933-722 - Each of 1

₹ 85,173.00

In Stock

Quantity

1

Base Price: ₹ 85,173.00

GST (18%): ₹ 15,331.14

Total Price: ₹ 1,00,504.14

Antigen

CASP1

Classification

Monoclonal

Conjugate

Unconjugated

Dilution

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) (20 ug/mL) Western Blot (0.5-2 ug/mL) The optimal working dilution should be determined by the end user.

Gene Alias

ICE/IL1BC/P45

Host Species

Mouse

Purification Method

Protein G purification

Regulatory Status

RUO

Gene ID (Entrez)

834

Content And Storage

Store at 4°C. For long term storage store at -20°C.Aliquot to avoid repeated freezing and thawing.

Isotype

IgG1 κ

Applications

Immunohistochemistry (PFA fixed), Western Blot

Clone

14F468

Description

Mouse monoclonal antibody raised against human CASP1.

Formulation

In PBS (0.05% BSA, 0.05% sodium azide).

Gene Symbols

CASP1

Immunogen

A synthetic peptide corresponding to amino acids 371-390 of human CASP1.

Quantity

50 μg

Primary or Secondary

Primary

Target Species

Human

Form

Liquid

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Description

  • This gene encodes a protein which is a member of the cysteine-aspartic acid protease (caspase) family
  • Sequential activation of caspases plays a central role in the execution-phase of cell apoptosis
  • Caspases exist as inactive proenzymes which undergo proteolytic processing at conserved aspartic residues to produce 2 subunits, large and small, that dimerize to form the active enzyme
  • This gene was identified by its ability to proteolytically cleave and activate the inactive precursor of interleukin-1, a cytokine involved in the processes such as inflammation, septic shock, and wound healing
  • This gene has been shown to induce cell apoptosis and may function in various developmental stages
  • Studies of a similar gene in mouse suggest a role in the pathogenesis of Huntington disease
  • Alternative splicing of this gene results in five transcript variants encoding distinct isoforms
  • [provided by RefSeq] Sequence: RKVRFSFEQPDGRAQMPTTE