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Anti-SOX9 Antibody (C-Terminus) LS-C144931

Catalog	Size	Price
LS-C144931-100	100 µl	Unavailable

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Reactivity:	Human, Mouse, Rat, Chicken, Frog, Zebrafish
Application:	Western blot
Format:	Unconjugated

Anti-SOX9 Antibody (clone 3C10) IHC-plus™ LS-B4420

Antibody:	Mouse Monoclonal [clone 3C10] (IgG2a,k) to Human SOX9
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Application:	IHC - Paraffin, Immunofluorescence, Western blot, ELISA
Format:	Unconjugated

Anti-SOX9 Antibody (clone 3F11) IHC-plus™ LS-B4421

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Anti-SOX9 Antibody (aa147-196) IHC-plus™ LS-B5761

Antibody:	Rabbit Polyclonal (IgG) to Human SOX9
Reactivity:	Human, Mouse
Application:	IHC - Paraffin, Immunofluorescence, Western blot, ELISA
Format:	Unconjugated

Anti-SOX9 Antibody (aa225-275) IHC-plus™ LS-B12075

Antibody:	Rabbit Polyclonal to Human SOX9
Reactivity:	Human, Mouse, Rat, Dog
Application:	IHC - Paraffin, Western blot
Format:	Unconjugated

Antibody:	Rabbit Polyclonal to Human SOX9
Reactivity:	Human
Application:	IHC, Western blot
Format:	Unconjugated

Details

Target:	Human SOX9
Host:	Rabbit
Reactivity:	Human (tested or 100% immunogen sequence identity)
Clonality:	Polyclonal
Conjugations:	Unconjugated
Purification:	Antiserum
Modifications:	Unmodified

Applications

Approved:

IHC (1:100 - 1:1000)
Western blot (1:500 - 1:5000)

Specificity and Use

Immunogen:	SOX9 antibody was raised against synthetic peptide derived from Cter domain of human SOX-9 protein
Epitope:	C-Terminus
Specificity:	Human 56 kD protein

Packaging

Presentation:	Lyophilized antiserum
Reconstitution:	100 µl Distilled water
Storage:	Long term: -20°C; Short term: +4°C; Avoid freeze-thaw cycles.
Restrictions:	For research use only.

About SOX9

Uniprot: P48436 NCBI: NM_000346 NP_000337.1

Synonyms: SOX9 Antibody, CMD1 Antibody, CMPD1 Antibody, SRY-related HMG-box, gene 9 Antibody, Transcription factor SOX-9 Antibody

Description: The SOX9 protein recognizes the sequence CCTTGAG along with other members of the HMG-box class DNA-binding proteins. It acts during chondrocyte differentiation and, with steroidogenic factor 1, regulates transcription of the anti-Muellerian hormone (AMH) gene. Deficiencies lead to the skeletal malformation syndrome campomelic dysplasia, frequently with sex reversal.

(More About SOX9)

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Date Requested: 8/17/2017

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