ARG65207

anti-HOXD13 antibody

anti-HOXD13 antibody for ICC/IF,IHC-Formalin-fixed paraffin-embedded sections and Human

Gene Regulation antibody

Overview

Product Description Goat Polyclonal antibody recognizes HOXD13
Tested Reactivity Hu
Predict Reactivity Ms, Rat, Cow
Tested Application ICC/IF, IHC-P
Host Goat
Clonality Polyclonal
Isotype IgG
Target Name HOXD13
Antigen Species Human
Immunogen C-KSSFPGDVALNQPD
Conjugation Un-conjugated
Alternate Names BDE; HOX4I; Homeobox protein Hox-4I; Homeobox protein Hox-D13; SPD; BDSD

Application Instructions

Application Suggestion
Tested Application Dilution
ICC/IF10 µg/ml
IHC-P1 - 2 µg/ml
Application Note IHC-P: Antigen Retrieval: Steam tissue section in Citrate buffer (pH 6.0).
* The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist.

Properties

Form Liquid
Purification Purified from goat serum by antigen affinity chromatography.
Buffer Tris saline (pH 7.3), 0.02% Sodium azide and 0.5% BSA.
Preservative 0.02% Sodium azide
Stabilizer 0.5% BSA
Concentration 0.5 mg/ml
Storage Instruction For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C or below. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use.
Note For laboratory research only, not for drug, diagnostic or other use.

Bioinformation

Database Links

GeneID: 3239 Human HOXD13

Swiss-port # P35453 Human Homeobox protein Hox-D13

Background This gene belongs to the homeobox family of genes. The homeobox genes encode a highly conserved family of transcription factors that play an important role in morphogenesis in all multicellular organisms. Mammals possess four similar homeobox gene clusters, HOXA, HOXB, HOXC and HOXD, located on different chromosomes, consisting of 9 to 11 genes arranged in tandem. This gene is one of several homeobox HOXD genes located in a cluster on chromosome 2. Deletions that remove the entire HOXD gene cluster or the 5' end of this cluster have been associated with severe limb and genital abnormalities. Mutations in this particular gene cause synpolydactyly. [provided by RefSeq, Jul 2008]
Research Area Gene Regulation antibody
Calculated MW 36 kDa