Sonic Hedgehog Protein (SHH) Antibody Pair

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1573€ (5 × 96 tests)

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935106861
info@markelab.com
name
Sonic Hedgehog Protein (SHH) Antibody Pair
category
Antibody Pairs
provider
Abbexa
reference
abx370329
tested applications
ELISA

Description

Sonic Hedgehog Protein (SHH) Antibody Pair for use in Sandwich ELISA assay development.
This antibody pair contains:
Detection: 50 µg
Capture: 200 µg
Standard: 2 µg

Documents del producto

Instrucciones
Data sheet
Descargar

Product specifications

Category
Antibody Pairs
Immunogen Target
Sonic Hedgehog Protein (SHH)
Reactivity
Rat
Assay Data
Sandwich
Assay Type
Capture Antibody: 0.5 mg/ml  Biotin-Conjugated Detection Antibody: 0.2 mg/ml
Reconstitute the standard with Standard Diluent. The volume, and therefore standard concentration, should be determined by the end user.
Recommended Dilution
Dilute the Capture Antibody 125-fold with Coating Buffer.  Dilute the Biotin-Conjugated Detection Antibody 200-fold with Detection Antibody Diluent.  Optimal dilutions/concentrations should be determined by the end user.
Conjugation
Biotin
Size 1
5 × 96 tests
Size 2
10 × 96 tests
Form
Standard form: Lyophilized
Capture Ab: Liquid
Detection Ab: Liquid
Tested Applications
ELISA
Buffer
The Capture and Detection Antibody both contain 0.1% sodium azide.
Availability
Please enquire.
Storage
Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles.
Dry Ice
No
Background
Antibody pair for SHH
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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FNab07847

SHH antibody

This gene encodes a protein that is instrumental in patterning the early embryo. It has been implicated as the key inductive signal in patterning of the ventral neural tube, the anterior-posterior limb axis, and the ventral somites. Of three human proteins showing sequence and functional similarity to the sonic hedgehog protein of Drosophila, this protein is the most similar. The protein is made as a precursor that is autocatalytically cleaved; the N-terminal portion is soluble and contains the signalling activity while the C-terminal portion is involved in precursor processing. More importantly, the C-terminal product covalently attaches a cholesterol moiety to the N-terminal product, restricting the N-terminal product to the cell surface and preventing it from freely diffusing throughout the developing embryo. Defects in this protein or in its signalling pathway are a cause of holoprosencephaly (HPE), a disorder in which the developing forebrain fails to correctly separate into right and left hemispheres. HPE is manifested by facial deformities. It is also thought that mutations in this gene or in its signalling pathway may be responsible for VACTERL syndrome, which is characterized by vertebral defects, anal atresia, tracheoesophageal fistula with esophageal atresia, radial and renal dysplasia, cardiac anomalies, and limb abnormalities. Additionally, mutations in a long range enhancer located approximately 1 megabase upstream of this gene disrupt limb patterning and can result in preaxial polydactyly.

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