HOXA13 Antikörper (C-Term)

Produktnummer ABIN5531398

Produktdetails anti-HOXA13 Antikörper

Target: HOXA13 (Homeobox A13 (HOXA13))

Bindungsspezifität: AA 356-383, C-Term

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser HOXA13 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Aufreinigung: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogen: This HOXA13 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 356-383 amino acids from the C-terminal region of human HOXA13.

Isotyp: Ig Fraction

Anwendungsinformationen

Applikationshinweise: For WB starting dilution is: 1:1000

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 0.5 mg/mL

Buffer: Supplied in PBS with 0.09 % (W/V) sodium azide.

Konservierungsmittel: Sodium azide

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

Lagerung: 4 °C,-20 °C

Informationen zur Lagerung: Store at 4°C for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.

Details zu HOXA13

Target: HOXA13 (Homeobox A13 (HOXA13))

Andere Bezeichnung: HOXA13 (HOXA13 Produkte)

Synonyme: HOXA13 antikoerper, RGD1562483 antikoerper, HOX1 antikoerper, HOX1J antikoerper, Hd antikoerper, Hox-1.10 antikoerper, homeobox A13 antikoerper, homeo box A13 antikoerper, HOXA13 antikoerper, Hoxa13 antikoerper

Hintergrund: 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. Expansion of a polyalanine tract in the encoded protein can cause hand-foot-uterus syndrome, also known as hand-foot-genital syndrome.

Molekulargewicht: 40 kDa

Gen-ID: 3209

UniProt: P31271