Complement C1s Subcomponent (C1S) Antibody

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195€ (20 µl)

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935106861
info@markelab.com
name
Complement C1s Subcomponent (C1S) Antibody
category
Primary Antibodies
provider
Abbexa
reference
abx005238
tested applications
WB

Description

C1S Antibody is a Rabbit Polyclonal antibody against C1S. This gene encodes a serine protease, which is a major constituent of the human complement subcomponent C1. C1s associates with two other complement components C1r and C1q in order to yield the first component of the serum complement system. Defects in this gene are the cause of selective C1s deficiency.

Documents del producto

Instrucciones
Data sheet
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Product specifications

Category
Primary Antibodies
Immunogen Target
Target: Complement C1s Subcomponent (C1S)
Immunogen: Recombinant protein corresponding to C1S. The exact sequence is proprietary.
Host
Rabbit
Reactivity
Human, Rat
Assay Type
Concentration: > 0.2 mg/ml
Recommended Dilution
WB: 1/500 - 1/2000. Optimal dilutions/concentrations should be determined by the end user.
Clonality
Polyclonal
Conjugation
Unconjugated
Isotype
IgG
Observed MW
Calculated MW: 77 kDa  Observed MW: 77 kDa
Purification
Purified by affinity chromatography.
Size 1
20 µl
Size 2
100 µl
Size 3
2 × 100 µl
Form
Liquid
Tested Applications
WB
Buffer
PBS, pH 7.3, containing 0.02% sodium azide, 50% glycerol.
Availability
Shipped within 5-10 working days.
Storage
Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles.
Dry Ice
No
UniProt ID
P09871
Gene ID
716
NCBI Accession
NP_958850.1
Background
Antibody anti-C1S
Status
RUO
Note
THIS PRODUCT IS FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC, THERAPEUTIC OR COSMETIC PROCEDURES. NOT FOR HUMAN OR ANIMAL CONSUMPTION.

Descripción

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Complement C1s Subcomponent (C1S) Antibody

C1S Antibody is a Rabbit Polyclonal antibody against C1S. This gene encodes a serine protease, which is a major constituent of the human complement subcomponent C1. C1s associates with two other complement components C1r and C1q in order to yield the first component of the serum complement system. Defects in this gene are the cause of selective C1s deficiency.

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