Homeobox A11 antibody (AA 1-180)

Catalog No. ABIN1680330

The Rabbit Polyclonal anti-Homeobox A11 antibody has been validated for WB and IF. It is suitable to detect Homeobox A11 in samples from Human.

Quick Overview for Homeobox A11 antibody (AA 1-180) (ABIN1680330)

Target: Homeobox A11 (HOXA11)

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This Homeobox A11 antibody is un-conjugated

Application: Western Blotting (WB), Immunofluorescence (IF)

Product Details anti-Homeobox A11 Antibody

Binding Specificity: AA 1-180

Sequence: MDFDERGPCS SNMYLPSCTY YVSGPDFSSL PSFLPQTPSS RPMTYSYSSN LPQVQPVREV TFREYAIEPA TKWHPRGNLA HCYSAEELVH RDCLQAPSAA GVPGDVLAKS SANVYHHPTP AVSSNFYSTV GRNGVLPQAF DQFFETAYGT PENLASSDYP GDKSAEKGPP AATATSAAAA

Cross-Reactivity: Human

Characteristics: Polyclonal Antibodies

Purification: Affinity purification

Immunogen: Recombinant fusion protein containing a sequence corresponding to amino acids 1-180 of human HOXA11 (NP_005514.1).

Isotype: IgG

Application Details

Application Notes: WB,1:500 - 1:2000,IF,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 Homeobox A11

Target: Homeobox A11 (HOXA11)

Alternative Name: HOXA11

Background: In vertebrates, the genes encoding the class of transcription factors called homeobox genes are found in clusters named A, B, C, and D on four separate chromosomes. Expression of these proteins is spatially and temporally regulated during embryonic development. This gene is part of the A cluster on chromosome 7 and encodes a DNA-binding transcription factor which may regulate gene expression, morphogenesis, and differentiation. This gene is involved in the regulation of uterine development and is required for female fertility. Mutations in this gene can cause radio-ulnar synostosis with amegakaryocytic thrombocytopenia.,HOXA11,HOX1,HOX1I,RUSAT1,Epigenetics & Nuclear Signaling,Transcription Factors,HOXA11

Molecular Weight: 34 kDa

Gene ID: 3207

UniProt: P31270