SOX9 antibody (AA 100-200)

Catalog No. ABIN1682861

The Rabbit Polyclonal anti-SOX9 antibody has been validated for WB and IHC. It is suitable to detect SOX9 in samples from Human.

Quick Overview for SOX9 antibody (AA 100-200) (ABIN1682861)

Target: SOX9 (SRY (Sex Determining Region Y)-Box 9 (SOX9))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This SOX9 antibody is un-conjugated

Application: Western Blotting (WB), Immunohistochemistry (IHC)

Product Details anti-SOX9 Antibody

Binding Specificity: AA 100-200

Sequence: KNKPHVKRPM NAFMVWAQAA RRKLADQYPH LHNAELSKTL GKLWRLLNES EKRPFVEEAE RLRVQHKKDH PDYKYQPRRR KSVKNGQAEA EEATEQTHIS P

Cross-Reactivity: Human, Mouse, Rat

Characteristics: Polyclonal Antibodies

Immunogen: A synthetic peptide corresponding to a sequence within amino acids 100-200 of human SOX9 (NP_000337.1).

Isotype: IgG

Application Details

Application Notes: WB,1:500 - 1:2000,IHC,1:50 - 1:200

Restrictions: For Research Use only

Handling

Buffer: PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: -20 °C

Storage Comment: Store at -20°C. Avoid freeze / thaw cycles.

Target Details for SOX9

Target: SOX9 (SRY (Sex Determining Region Y)-Box 9 (SOX9))

Alternative Name: SOX9

Background: The protein encoded by this gene 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.,CMD1,CMPD1,SRA1,SRXX2,SRXY10,SOX9,SRY-box 9,Epigenetics & Nuclear Signaling,Transcription Factors,Cell Biology & Developmental Biology,Apoptosis,Neuroscience,Stem Cells,Mesenchymal Stem Cells,Neural Stem Cells,SOX9

Molecular Weight: 56 kDa

Gene ID: 6662

UniProt: P48436

Pathways: EGFR Signaling Pathway, Stem Cell Maintenance, Regulation of Muscle Cell Differentiation, Tube Formation, Skeletal Muscle Fiber Development